Clinicopathological Characteristics and Outcomes of Patients With Endometriosis-Related Hemorrhagic Ascites: An Updated Systematic Review of the Literature

The presence of ascites is a common clinical presentation in gynecologic oncology patients. Hemorrhagic ascites (HA) due to endometriosis is a rare presentation that can be easily misdiagnosed as ovarian malignancies. The present study aims to update the currently available knowledge on the characteristics of patients presenting with HA due to endometriosis. A systematic search was conducted for articles published from January 2000 to July 2020 using the Medline, Scopus, and Google Scholar databases along with the references of the full-text articles retrieved. Papers describing cases of women over 18 years with or without previous history of endometriosis were assessed. Only cases with histologically proven hemorrhagic ascites of endometriosis origin were included. Twenty-nine studies (27 case reports and two case series) comprising 32 patients were evaluated. The mean patients’ age was 32 years, while six of the patients had a previous history of endometriosis. The mean amount of drained ascitic fluid was 4,200 mL, whereas three patients underwent thoracentesis due to pleural effusions. The treatment options included not only medical but also surgical therapies. Fertility preservation was achieved in 27 patients, while two of them achieved pregnancy with in vitro fertilization (IVF) techniques. Endometriosis-related hemorrhagic ascites is a relatively rare expression of the disease. Endometriosis- related hemorrhagic ascites should be considered in the differential diagnosis (DD) of women with ascites and clinical suspicion of endometriosis. The available literature is limited to case reports and case series and thus indicates further research in the field to decode the pathophysiology of the disease and decide on the optimal treatment. Categories: Obstetrics/Gynecology

hemorrhagic, ascites, hemoperitoneum, ovarian cancer, endometriosis

And Background Ascites is the accumulation of fluid in the peritoneal cavity and are typically presented with abdominal distension, tenderness, dyspnea, and fatigue [1] . The differential diagnosis (DD) of ascites is complicated by atypical symptoms and the wide variety of diseases included and thus disabling the final diagnosis [2] . In that setting, the most common cause of ascites is hepatic cirrhosis due to portal hypertension, which accounts for approximately 80% of ascites DD [3] . Among the other causes, peritoneal disease (cancerous, infectious, or inflammatory), hypoalbuminemia (nephrotic syndrome), and rare conditions (chylous, pancreatic, urinary, and hemoperitoneum) have also been reported in the etiology of peritoneal fluid concentration [4] . Hemorrhagic (or bloody) ascites have been reported as the presence of red blood cells (RBC) ≥ 10,000 per mm 3 , while in dark blood-colored ascitic fluid, about 50,000 RBCs per mm 3 have been measured [5] . From the point of view of gynecology, ascites is a frequent presentation in women with ovarian malignancies investigated in gynecologic oncology clinics [6] . In addition to this, there are also various benign gynecologic diseases that have been characterized by the presence of ascites, including ovarian hyperstimulation syndrome, Meigs syndrome, benign ovarian tumors, fibroids, and endometriosis, which makes the final diagnosis difficult to be established [7] . Paracentesis and cytological examination of the ascitic fluid is a simple procedure but with limited diagnostic accuracy. 1 1 1 2 3 4 1 1 Open Access Review Article DOI: 10.7759/cureus.26222 How to cite this article Pandraklakis A, Prodromidou A, Haidopoulos D, et al. (June 22, 2022) Clinicopathological Characteristics and Outcomes of Patients With Endometriosis-Related Hemorrhagic Ascites: An Updated Systematic Review of the Literature. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 Endometriosis is a common benign gynecologic disorder that is mainly found in women of reproductive age and is defined as the presence of endometriotic tissue in areas outside the uterine cavity [8] . The pelvic structures and organs are the most prevalent sites of endometriosis despite the fact that in rare cases endometriotic lesions can grow in extrapelvic sites [9] . Hemorrhagic ascites (HA) associated with endometriosis is a rare entity that creates diagnostic dilemmas for gynecologists and complicates the management of the disease. The aim of the present study was to update the currently available knowledge on the characteristics of patients presenting with HA due to endometriosis. More specifically, given the lack of specific guidelines and consensus on the appropriate management, we sought to investigate the potential mechanisms of endometriosis-related ascites formation, clinical presentation, and disease characteristics, as well as the type of interventions for the management of the disease and postoperative outcomes. Review

Study Design and Eligible Studies The present systematic review was performed in accordance with the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) according to the authors’ predetermined inclusion criteria [10] . Three authors (APr, APan, and NT) independently and meticulously searched the literature, excluded overlaps, and structured the tables with the selected indices. All appropriate observational studies (prospective and retrospective) and case reports and case series of patients with a diagnosis of endometriosis-related HA were considered eligible for inclusion in the present study. The cases with hemorrhagic peritoneal fluid due to endometriosis were considered eligible, while cases of hemoperitoneum related to rupture of ovarian endometrioma or other endometriotic nodules were excluded. Additionally, those reported respective cases of HA and hemoperitoneum during pregnancy were also not included. Cases describing the identification of ascetic fluid in which the paracentesis revealed “yellow” fluid were also not included. Review articles, conference papers, abstracts, letters to the editor, and animal studies were excluded from analysis and tabulation. Additionally, video articles that were accompanied by abstracts with insufficient data were also excluded. Only articles written in the English language were included. Search Strategy and Data Collection We performed a meticulous and systematic search of the literature for articles published from January 2000 to July 2020 using the Medline (2000-2020), Scopus (2000-2020), and Google Scholar (2000-2020) databases along with the references of the articles that were retrieved in full text. The following keywords were used for the search: “endometriosis,” “hemorrhagic ascites,” “hemoperitoneum,” and “bloody ascites.” A minimum number of search keywords were utilized in an attempt to assess an eligible number that could be easily searched while simultaneously minimizing the potential loss of articles. Articles that fulfilled or were deemed to fulfill the inclusion criteria were retrieved; all articles describing cases of women aged >18 years with or without previous history of endometriosis who were diagnosed with HA that was histologically proven to be of endometriosis origin were included. The PRISMA flow diagram schematically presents the process of article selection (Figure 1 ). 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 2 of 13 FIGURE 1: Search flow diagram Our search strategy included the following MeSH terms: (“blood” (MeSH Subheading) OR “blood” (All Fields) OR “blood” (MeSH Terms) OR “bloods” (All Fields) OR “haematology” (All Fields) OR “hematology” (MeSH Terms) OR “hematology” (All Fields) OR “haematoma” (All Fields) OR “hematoma” (MeSH Terms) OR “hematoma” (All Fields) OR “haemorrhage” (All Fields) OR “hemorrhage” (MeSH Terms) OR “hemorrhage” (All Fields) OR “haemorrhages” (All Fields) OR “hemorrhages” (All Fields) OR “haemorrhagic” (All Fields) OR “haemorrhaging” (All Fields) OR “hematologies” (All Fields) OR “haematomas” (All Fields) OR “hematomas” (All Fields) OR “hematomas” (All Fields) OR “hematomae” (All Fields) OR “hemorrhaged” (All Fields) OR “hemorrhagic” (All Fields) OR “hemorrhagical” (All Fields) OR “hemorrhaging” (All Fields)) AND (“ascite” (All Fields) OR “ascites” (MeSH Terms) OR “ascites” (All Fields) OR “ascitic” (All Fields)) AND (“endometriosis” (MeSH Terms) OR “endometriosis” (All Fields) OR “endometrioses” (All Fields)). Outcomes Retrieved The management of the disease and recurrences and reoperation rates during follow-up were set as the main outcomes of the present study. Concerning the secondary findings of our study, the characteristics of the disease, including the concomitant presence of pleural effusion, clinical presentation and symptomatology, type of diagnostic procedure, amount of fluid drained recurrence rates, and follow-up after the last treatment, were appraised. Additionally, levels of CA 125 (for studies with multiple values, we considered the highest one) and hemoglobin were evaluated. Data on patient characteristics included age, ethnicity, parity, and gravidity of women. Definitions Hemorrhagic ascites is defined as the detection of more than 10,000 red blood cells (RBC) per μ L in the ascitic fluid. However, when RBC count in the ascitic fluid was not available, the diagnosis of HA was based on the radiographic findings and/or macroscopic appearance of the bloody/dark red color of the fluid drained. Quality Assessment 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 3 of 13 Case reports and case series are associated with elevated bias due to the nature of those types of studies [11] . Nonetheless, in the case where data on a certain condition is limited, evidence from those studies is considered of clinical importance. We evaluated the quality of the enrolled studies by adopting the quality assessment tool for case reports and case series proposed by Murad et al. [11] . More specifically, the methodological quality of the studies was assessed based on the criteria, including the domains of ascertainment, causality, selection, and reporting. The sum of the scores derived from eight critical questions that referred to the domains was used to evaluate the quality of each study and the reviewer’s judgment on the presence of the most important domains according to a certain clinical case. Statistical Analysis Continuous variables were interpreted as median and range, while categorical variables as frequencies and percentages. The level of statistical significance was set at p < 0.05.

Included and Excluded Studies A total of 34 full-text articles were assessed to figure out the eligible studies. Among them, 29 studies (27 case reports and two case series) that recruited 32 patients were considered eligible for inclusion [12-40] , while the remaining five were excluded with reasons [41-45] . The study by Kishino et al. was excluded due to the fact that the hemorrhagic peritoneal fluid was attributed to retrograde menstruation, whereas the study by Bean et al. was excluded due to insufficient data [41,45] . More specifically, three studies were excluded due to the fact that the full text could not be reached despite multiple attempts to contact the journal and authors [42-44] . Patient Characteristics The median age of the 32 included patients was 32 years (range: 21-46 years). Data concerning ethnicity was available for 14 patients. More specifically, nine patients were of African origin (African-American, Afro- Brazilian, Afro- Caribbean, and Nigerian), while two patients were Caucasian, one was Hispanic, and two were Asian. Regarding the 26 patients with parity information available, 19 patients were nulliparous, whereas four were primiparous, and the remaining three were multiparous. Six patients reported a previous history of endometriosis, five of whom underwent an exploratory laparoscopy for the diagnosis and management of the disease. The median CA 125 values were 184 U/L (range: 22 to >5,009), as reported by 16 studies, while the median values for hemoglobin were 9.8 g/dL (range: 6.9-12.9 g/dL), which were data from 12 studies. Six patients were diagnosed with the presence of concomitant pleural effusion. Abdominal distention and progressively worsened discomfort were reported as the main symptoms, followed by abdominal pain, weight loss, anorexia, fever, nausea, and breathing difficulty (Table 1 ). Author and year Age Ethnicity History of EM G/P Pleural effusion CA 125 (U/mL) Hb (g/dL) Clinical symptoms Clinical examination findings Diagnosis (imaging or drainage) Bhojawala et al. (2000) [12] 34 Black No G0P0 Yes N/A 11.4 Abdominal distension (four months), malaise, loose stools, nausea and vomiting (two weeks), shortness of breath, appetite loss Tense and distended abdomen, hyperactive bowel sounds, positive fluid thrill Laparotomy Dias et al. (2000) [13] 41 Black No G0P0 No N/A N/A No N/A Exploratory laparotomy Cheong et al. (2003) [14] 41 Malay No P1 Yes Normal Normal Worsening abdominal distension Gross ascites Paracentesis Goumenou et al. (2006) [15] 46 N/A Yes, laparoscopy (30 years old), infertility G3P0 Yes, bilateral 3,504 10.2 Progressive dyspnea, abdominal distension, nausea, 7 kg weight loss Tachypnea, ↓breath sounds, abdominal distension, fever Thoracocentesis, paracentesis Alabi et al. (2007) [16] 30 Black African Yes, vaginal EM, six months, GnRH analog and goserelin N/A No 56 8.5 Abdominal distension and pain during IVF treatment with GnRH agonist N/A Paracentesis Palayekar et al. (2007) [17] N/A African- American No P1 No 33.6 N/A Abdominal distension, anemia Moderate abdominal distension Paracentesis Santos et Yes, laparoscopy 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 4 of 13 al. (2007) [18] 40 Brazilian (longstanding amenorrhea) G0P0 No N/A N/A Upper abdominal pain, vomiting and weight loss of 11 kg, anemia N/A Paracentesis Sait (2008) [19] 26 N/A No P0 No 3,140 N/A Increased abdominal girth Distended abdomen Laparotomy Ussia et al. (2008) [20] 26 Caucasian Yes, thoracic and diaphragmatic G0P0 No Ν/A N/A Ascites N/A Laparoscopy 23 N/A No G0P0 Yes N/A N/A Severe dysmenorrhea and menstrual R shoulder pain N/A Thoracocentesis (twice) Day et al. (2009) [21] 24 N/A No, EM-related symptoms G0P0 No N/A 10.7 Two-year abdominal pain, nausea, vomiting, constipation, infertility N/A Paracentesis turbid brown fluid Lin et al. (2010) [22] 29 N/A No G2P2 Yes N/A 12.9 Light-headedness, palpitations Hypovolemic shock Paracentesis Suchetha et al.(2010) [23] 36 N/A No Parous No >5,000 N/A Massive ascites Nodularity in Douglas Paracentesis, laparotomy Fernandes et al. (2011) [25] 28 Afro- Brazilian No G0P0 No N/A 9.5 Progressive increase in abdominal girth, weight loss Distended, nontender abdomen, positive shifting dullness Paracentesis Shabeerali et al. (2012) [24] 28 N/A No N/A No N/A N/A Abdominal distension (five weeks) Ascites and mild tenderness Paracentesis 30 N/A No P2 No 96 N/A Progressive abdominal distension and weight loss N/A Paracentesis 40 N/A No G6P4 No N/A N/A Ascites Ascites Paracentesis Morgan et al. (2013) [26] 27 African Yes, COC G0P0 No N/A 7 R neck and flank pain, light-headedness, and palpitations Mildly distended abdomen, tender in the RUQ Paracentesis Mumtahana et al. (2014) [27] 36 Chinese Yes G0P0 No 78.23, 86.6, 5,009 N/A Ascites, anemia Abdominal distension Paracentesis Appleby et al. (2014) [28] 34 Nigerian No N/A No N/A 9.6 Abdominal distention, 4 kg weight loss Gross ascites Drainage Asano et al. (2014) [29] 35 Japanese No G0P0 No 22 10 Dysmenorrhea, abdominal distention Abdominal distention Drainage Bignall et al. (2014) [30] 36 Afro- Caribbean No G0P0 No 1123 10.8 Seven-month dysmenorrhea, deep dyspareunia, constipation Abdominal tenderness and distention Paracentesis Cosma et al. (2014) [31] 36 N/A Deep pelvic EM N/A No 184 N/A Dysmenorrhea, dyschezia, epigastric menstrual pain N/A Drainage Hasdemir et al. (2014) [32] 32 N/A Yes, EM (laparoscopic biopsies) N/A Yes 47 N/A Abdominal distension and shortness of breath Massive ascites Laparoscopy, drainage Hinduja et al. (2015) [33] 34 N/A No P1A1 No N/A N/A Abdominal bloating N/A Transvaginal aspiration of Douglas Setubal et al. (2015) [40] 26 Caucasian No G0P0 No 100 N/A Upper abdominal pain and distention N/A Paracentesis Dun et al. 26 Nigerian Yes P0 No N/A N/A Ascites N/A Drainage 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 5 of 13 (2016) [34] Pereira et al. (2017) [35] 21 N/A No G0P0 No N/A 7.5 Abdominal distension, dyspnea N/A Laparoscopy Magalhães et al. (2018) [36] 28 N/A No N/A No 107.8, 889.6 N/A Wasting syndrome, ↑abdominal girth, shortness of breath,c↓appetite N/A Diagnostic laparoscopy Pang et al. (2019) [37] 40 N/A No G1P0 No 372.4 N/A Lower abdominal pain, pelvic mass, dysmenorrhea Palpable pelvic mass Laparoscopy Wang et al. (2019) [38] 24 Nigerian No G0P0 No 41.54, 113 6.9 Rapidly enlarging abdominal distension Massive ascites N/A Gonzalez et al. (2020) [39] 32 Hispanic Yes, massive hemorrhagic ascites Null N/A N/A N/A Malaise, abdominal distension, loss of appetite, diffuse abdominal pain, breathing difficulty N/A Paracentesis TABLE 1: Main characteristics of the included studies R: right, RUQ: right upper quadrant, EM: endometriosis, G: gravidity, P: parity, Hb: hemoglobin, N/A: not available, COC: combined oral contraceptives Additionally, endometriosis-related symptoms including dysmenorrhea, dyspareunia, and dyschezia were also recorded. Clinical examination revealed abdominal tenderness and distention with shifting dullness in palpation, palpable pelvic mass if present, and diminished breath sound in patients with simultaneous pleural effusion. In critically ill patients, signs of hemodynamic instability were also noted. In 19 cases, the diagnosis was established with an examination of the percutaneously drained HA, while in one patient, a transvaginal paracentesis through the pouch of Douglas was performed. Five patients underwent an exploratory laparoscopy and drainage, whereas an open surgical approach was applied to three women. Quality Assessment Based on the type of the included clinical cases, we considered the score of 5 points as the highest that could be assessed when excluding the three questions (from 4 to 6) from the quality assessment tool that attributed to cases of adverse drug events. A mean score of 3.5 (SD: ±0.85) was calculated, whereas the overall judgment on the quality of the recruited studies was that they were of moderate quality. Main Outcomes The median amount of fluid drained was 4,200 mL (range: 1,500-9,400 mL), and four patients underwent two or more sessions of paracentesis. Concomitant thoracentesis was performed three patients due to pleural effusion. The main treatment modalities included hormonal therapy, other medications for symptomatic relief, and surgical procedures. Various hormonal modalities were adopted, including GnRH agonists/analogs (goserelin and leuprorelin), combined oral contraceptives (COC), luteinizing hormone (LH) agonists, dienogest, medroxyprogesterone, and norethindrone. GnRH agonist treatment was used in 17 patients, GnRH antagonists in one patient, COC in three patients, LH agonist in one patient, dienogest in two patients, and medroxyprogesterone and norethindrone in one patient. There is a case that was treated with chemotherapeutic agents for suspected ovarian cancer [15] and two cases that were initially treated with antituberculous agents for suspected tuberculous ascites [24,38] . Therapy with fertility- preserving management was decided in all but five patients at the initial management and included resection of all visible endometriotic nodules, adhesiolysis, and respective repairs of the affected organs such as colectomies and anastomosis, as shown in Table 2 . However, fertility was finally preserved in 27 patients. Seven patients underwent bilateral salpingo-oophorectomy with hysterectomy along with excision of all macroscopic pelvic endometriotic nodules and other procedures including omentectomy, appendectomy, and lymphadenectomy (Table 2 ). In 13 patients, an open approach was applied, whereas 24 patients had laparoscopic procedures. Six of them underwent both laparoscopic and laparotomic evaluation. Pregnancy outcomes were available for two patients who achieved a single and twin pregnancy [30,40] . Both of them conceived with the use of in vitro fertilization (IVF) techniques and delivered preterm through cesarean section at 32 and 35 weeks of gestation, respectively. Two of the patients had postoperative ileus; among them, one died due to peritonitis and sepsis after intestinal obstruction and enterocutaneous fistulae. Author Amount of fluid Management Histology Follow-up (recurrence- 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 6 of 13 and year drained Primary treatment Secondary treatment reoperation) Bhojawala et al. (2000) [12] 9,000 Laparotomy, TAH-RSO, adhesions N/A Endometriosis of the cervix, R fallopian tube, and ovary One mo - R exploratory thoracotomy, decortication of the R lung, and parietal pleurectomy; six wks - NED Dias et al. (2000) [13] N/A GnRH analog N/A N/A Six mo - progressive ↓ of ascites Cheong et al. (2003) [14] 5,600 Exploratory laparotomy-peritoneal biopsies Yes, medical EM N/A Goumenou et al. (2006) [15] 4,000 First-line chemotherapy (carboplatin/taxol), suspected malignancy Two mo - exploratory laparotomy debulking/TAH-BSO, omentectomy, appendectomy, biopsies, L pelvic lymphadenectomy Inflammation and EM Six mo - NED Alabi et al. (2007) [16] 5,000 Emergent diagnostic laparoscopy, extensive pelvic EM including the bowel Second laparoscopy after one wk, adhesiolysis, and bowel mobilization EM Two mo - ascites (2.5 L), recurrence; one mo - laparoscopy multiple biopsies; spontaneous conceive Palayekar et al. (2007) [17] 4,000- 6,000 Exploratory laparotomy - advanced pelvic EM, TAH-BSO Declined hormonal therapy EM 12 mo - NED Santos et al. (2007) [18] N/A Laparoscopy (nondiagnostic), laparotomy - adhesiolysis, encapsulating peritonitis N/A EM Five mo - intestinal obstruction, enterocutaneous fistulae, DOD (peritonitis and sepsis) Sait (2008) [19] 5,000 Laparotomy - bilateral ovarian cystectomy, multiple biopsies GnRH analog for six mo, maintenance with COC EM 12 mo - NED Ussia et al. (2008) [20] 1,000, >1,000, 2,000, 1,500 Three laparoscopies during three yrs, two mo laparotomy - massive adhesiolysis, appendicectomy, omentectomy, USO GnRH EM 36 mo - NED 1,500 Laparoscopy - ascites, frozen pelvis, bowel adhesions, and EM spots; second laparoscopy (one yr after GnRH agonist) - ascites, adhesions, DIE, rectovaginal nodule excision, ureterolysis, resection sigmoid anastomosis GnRH agonist and intermittent corticosteroids EM NED Day et al. (2009) [21] 4,000 Exploratory laparoscopy - stage IV ASRM EM, multiple biopsies Leuprolide acetate 11.25 mg EM Ileus PO (44-d admission - conservative management), three mo - NED Lin et al. (2010) [22] 2,000 Diagnostic laparoscopy - electrocauterization EM of the L broad ligament N/A N/A N/A Suchetha et al.(2010) [23] 6,000 Diagnostic laparotomy - abdominal cocoon, biopsies of the adnexa, bladder, peritoneum, omentum, and stomach One yr - leuprolide Three mo - bilateral ovarian masses, hydronephrosis - omentectomy Fernandes et al. 9,400 Laparoscopy - adhesions, mesosigmoid biopsy Three mo - GnRH analog estrogen and then continuous Fibrosis and extensive hemosiderin deposition, 12 mo - NED 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 7 of 13 (2011) [25] estrogen-progestin endometrial glands and stroma Shabeerali et al. (2012) [24] N/A Diagnostic laparoscopy conversion to laparotomy, dense adhesions with small and large bowel, biopsies; second operation TAH-BSO One yr - GnRH analogs (partial response), TAH-BSO N/A 12 mo - NED N/A Laparoscopy - ascites, peritoneal biopsies Subtotal hysterectomy and BSO EM 12 mo - NED 2,500, 3,000 Two laparoscopies - suspected tuberculosis (antituberculosis treatment); third laparoscopy - ascites, adhesions, biopsies GnRH analogs Endometrial glands and endometrioid stroma NED Morgan et al. (2013) [26] 4,500 Leuprolide N/A N/A N/A Mumtahana et al. (2014) [27] 3,000, 2,500 Exploratory laparoscopy, dense adhesions, bilateral ovarian masses, Douglas nodules Goserelin acetate/mo EM NED Appleby et al. (2014) [28] N/A Laparoscopy - endometrial ovarian and fallopian tube deposits (biopsies) GnRH antagonist EM Six mo - NED Asano et al. (2014) [29] 5,500 Exploratory laparotomy - adhesions, biopsies of brown omental nodules stage IV EM Eight y - GnRH agonist and ascites drainage (13 times) - switch to DNG EM 12 mo - NED Bignall et al. (2014) [30] 3,500, 1,600 Laparoscopy - biopsies of uterosacral ligament and bowel nodules stage IV EM GnRH analogs Cyclical endometrium in proliferative phase Pregnancy achieved (IVF) - live birth at 32 wks emergent CS/two wks recurrent ascites - 5 GnRH injections NED Cosma et al. (2014) [31] 4,200, 250 Laparoscopy - adhesions, excision of pelvic EM, colectomies, three anastomoses, and temporarily ileostomy Second-look laparoscopy and ileostomy closing (22 days) EM 48 mo - NED Hasdemir et al. (2014) [32] 2,500 Paracentesis and six mo leuprorelin N/A EM by paracentesis Three mo - recurrence - DNG Hinduja et al. (2015) [33] 4,500, 2,500, 3,000, 4,000, 3,500 Diagnostic laparoscopy - biopsies of omental and bowel nodules Three mo - leuprolide 3.75 mg EM Six mo - multiple recurrences of ascites, recurrence of ascites after TAH-BSO with vaginal discharge/one y - NED Setubal et al. (2015) [40] 2,500, 1,000 Diagnostic laparoscopy - pelvic adhesions, rectal and ovarian implants, omental retractions, hematic liver implants, multiple biopsies Three mo - COC EM Three mo - ascites recurrence-GnRH agonist; second laparoscopy - DIE, GnRH agonist; pregnancy achieved, live birth of twins at 35 weeks/NED on COC Dun et al. (2016) [34] 7,000, 7,800 Exploratory laparotomy - biopsies Three mo - goserelin and oral and one y oral medroxyprogesterone EM Three mo - recurrence, unsuccessful conceive attempt; laparoscopy, EM resection with peritoneal stripping, laser excision, ablation; six mo - NED Pereira et Laparoscopy (third laparoscopy) - 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 8 of 13 al. (2017) [35] 4,000 extensive EM adhesions in the pelvis, bipolar and monopolar excision of EM Monophasic oral contraceptive pills EM NED Magalhães et al. (2018) [36] 8,000 Diagnostic laparoscopy - multiple adhesions and encapsulating peritonitis (nondiagnostic); second laparoscopy - biopsies Goserelin acetate Chronic peritonitis and hemosiderin deposits Six mo - NED Pang et al. (2019) [37] 2,000 Laparoscopy converted to laparotomy (bleeding) - TAH BSO, R broad ligament mass excision No Mass with a monolayer of normal-looking endometrial glands and stroma Three mo - NED Wang et al. (2019) [38] N/A GnRH analogs (leuprorelin) for three mo and then droperidol and ethinyl estradiol tb for eight mo No Endometrial glandular cells and surrounding stromal cells (core needle biopsy of the omentum) Five mo - stable ascites - symptom improvement TABLE 2: Main outcomes N/A: not available, EM: endometriosis, R: right, L: left, PO: postoperative, wk: week, mo: months, yr: year, TAH: total abdominal hysterectomy, BSO: bilateral salpingo-oophorectomy, USO: unilateral salpingo-oophorectomy, COC: combined oral contraceptive, CS: cesarean section, NED: no evidence of disease, DOD: die of disease, DIE: deep infiltrating endometriosis, DNG: dienogest

In the present study, we analyzed the characteristics of 32 women with EM-related hemorrhagic ascites. The majority of patients were nulliparous, while abdominal distention and progressively worsened discomfort were recorded as the main symptoms at presentation. The mean amount of drained ascitic fluid was 4,200 mL. The treatment options included not only medical-hormonal but also surgical therapeutic modalities. Fertility preservation was achieved in 27 patients, while two of them achieved pregnancy with IVF techniques. Two cases of postoperative ileus were reported and one postoperative death due to peritonitis. The role of elevated CA 125 levels is debatable; there have been reports indicating elevated CA 125 levels in patients with ascites that are non-cancer-related, such as cirrhotic or even in heart failure [46,47] . According to the findings of the present study, CA 125 levels ranged from 22 to 5,000, which could be considered conflicting given the high suspicion of malignancy in patients with ascites and elevated CA 125 levels. Furthermore, before confirming the presence of ascites with ultrasound, there are also some percussion signs including puddle signs, floating ice, and flank dullness that could be useful [48] . The reported overall accuracy of physical examination maneuvers is approximately 58%, with sensitivity and specificity ranging from 50% to 94% and from 29% to 82%, respectively [49] . The differential diagnosis of a woman who presents with ascites is relatively challenging. Besides hepatic and renal failure, which are considered the main causes of the formation of ascites, malignant and infectious intra-abdominal diseases are also responsible for the concentration of diffusion of peritoneal fluid rich in proteins [50] . With regard to malignant diseases, epithelial ovarian and tubal cancer, primary peritoneal serous carcinoma, and endometrial cancer can be associated with ascites formation [51] . Furthermore, benign ovarian cysts, endometriosis, ovarian hyperstimulation syndrome, peritoneal tuberculosis, and Meigs syndrome should also be considered in the differential diagnosis of female ascites [51] . Endometriosis-related ascites can be easily misdiagnosed as ovarian cancer-related due to the fact that both entities share some similar symptoms. To that end, hemorrhagic endometriotic ascites can present with abdominal distention and pain, loss of appetite, and weight loss, mimicking atypical cancer symptoms. However, careful evaluation of patients’ medical history and endometriosis-related symptoms such as dysmenorrhea, dyspareunia, and cyclical pain should be thoroughly investigated. Furthermore, high clinical suspicion should be paid to the cases of malignancy arising from endometriosis [52] . The prevalence of malignancy is about 0.7%-1.6% in patients with endometriosis [52] . Consequently, the exclusion of malignancy is of critical importance, and thus, it is considered safer to set the final diagnosis after surgical evaluation and histological examination of the excised specimens. In that setting, some of the patients included in the present study underwent a diagnostic laparoscopy with a concomitant aspiration of the ascitic fluid and peritoneal biopsies. The percutaneous aspiration of the ascites has also been applied in 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 9 of 13 some cases. This first-line diagnostic modality is an easy-to-perform bedside practice and can facilitate a more accurate further management of the disease [53] . The cytological findings of the aspired ascitic fluid can reveal epithelial and stromal cells in a hemorrhagic environment with hemosiderin and hemofuscin- laden macrophages [53,54] . There are some reports available in the literature indicating the concomitant detection of encapsulating peritonitis in patients with endometriosis-related ascites. Encapsulating peritonitis, also known as abdominal cocoon or frozen ascites, is a rare entity defined as the formation of a thick fibrin membrane that entraps the bowel loops [36] . According to a recent systematic review by Magalhães et al. on endometriosis- related ascites and encapsulating peritonitis, only six cases of endometriosis-associated encapsulating peritonitis have been recorded in the literature [18,36] . Additionally, another case of encapsulating peritonitis has been recently published by Gonzalez et al. and was attributed to recurrent HA due to endometriosis [39] . A potential theory supports that endometriosis-related inflammation causes peritoneal irritation and further enhances fibrosis and inflammation, resulting in the formation of encapsulating peritonitis. The exact pathophysiology of the formation of endometriosis-related ascites still remains ill-defined. Bernstein et al. were the first to study on the pathogenesis of endometriosis-associated ascites. The authors claimed that the presence of endometrial cells in the peritoneal cavity under unknown mechanisms can activate the peritoneal cells to produce ascitic fluid [54] . Additionally, another theory suggested the peritoneal irritation from the spontaneous rupture of endometriotic cysts, which can produce reactive peritoneal fluid [54] . Another potential mechanism is based on the inflammatory response caused by the effect of the uterine hormones on the ectopic endometriotic lesions [55] . The aforementioned theories are well supported by recent studies speculating on the diversity of the biochemical and metabolic profiles of the peritoneal fluid in patients with endometriosis. More specifically, according to Polak et al., the hemoglobin levels in the peritoneal fluid of patients with endometriosis were significantly elevated compared to both controls and women with ovarian cysts, while, interestingly, antioxidant parameters were significantly lower in patients with endometriosis, creating an oxidative intraperitoneal environment [56- 58] . The outcomes of the present study indicated a high prevalence of HA in patients of African origin. A respective high prevalence was also observed in the systematic review by Gungor et al. who reported a proportion of more than 60% of African ethnicity among women with endometriosis-related ascites [54] . Little is known with regard to the potential association between endometriosis and race. Despite the fact that the currently available literature provides evidence of a higher prevalence of endometriosis in White women compared to African, those reports are subjected to significant bias related to diversity in socioeconomic status, access to the healthcare system, and childbearing age [59] . Additionally, Bougie et al. highlighted the potential diversity of symptoms and clinical presentation of endometriosis among different ethnicities, which could also explain the elevated prevalence of HA among African populations with endometriosis [59,60] . Concerning the management of endometriosis-associated ascites, it is mainly based on the extent of the underlying endometriosis and is that of endometriosis including surgery or medication or both. Additionally, the drainage of the ascetic fluid is crucial for the alleviation of abdominal distention and discomfort. Due to the fact that a significant proportion of patients (six in the present study) presented with concomitant pleural effusion, thoracentesis is also indicated for the symptomatic relief of breath discomfort. The majority of the patients in the present study underwent surgery for the management of endometriosis. The extent of surgical procedures is based on the age of the patient and the desire for fertility preservation [61] . Moreover, adjuvant pharmaceutical therapy was administered to 16 patients postoperatively. A favorable effect of postoperative medication maintenance therapy has been reported for symptomatic relief and recurrence prevention, but its exact role still remains controversial [61,62] .

Despite the plethora of reports, the true prevalence of HA could not be precisely reached since no observational studies are available in the field and thus precluded further research. The fact that our results are based only on case reports and two case series constitutes the main limitation of the study and precludes generalization of the conclusions and further quantitative and qualitative analysis. In addition to this, there is no sufficient evidence concerning the pathophysiology of ascites formation, while it is not clear for all cases whether the bloody peritoneal fluid was concentrated after the rupture of an ovarian endometrioma or whether other mechanisms similar to those forming malignant ascites are involved. Finally, there is significant heterogeneity in the included studies, and some parameters were omitted by some studies, which was another limitation and precluded reaching firm results.

The present review accumulates the current knowledge with regard to the natural history, characteristics, and management of adult females who presented with hemorrhagic ascites due to endometriosis. The differential diagnosis of a woman who presents with ascites is relatively challenging. Endometriosis-related 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 10 of 13 hemorrhagic ascites is a relatively rare expression of the disease. Nonetheless, it should be considered in the differential diagnosis of women with ascites and clinical suspicion of endometriosis. Additionally, the exclusion of malignancy is considered of critical importance. High clinical suspicion should be paid to cases of malignancy arising from endometriosis. The exact pathophysiologic pathways of endometriotic hemorrhagic ascites formation still remain elusive, despite the plethora of available theories. The management of hemorrhagic ascites should speculate on both alleviation of the abdominal distention due to the presence of ascites and treatment of the underlying disease. The currently available literature is limited to case reports and case series, thus precluding reaching firm conclusions. Further research in the field is needed to decode the pathophysiology of the disease and decide on the optimal treatment. Additional Information Disclosures Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

1 . Cavazzoni E, Bugiantella W, Graziosi L, Franceschini MS, Donini A: Malignant ascites: pathophysiology and treatment . Int J Clin Oncol. 2013, 18:1-9. 10.1007/s10147-012-0396-6 2 . Ford CE, Werner B, Hacker NF, Warton K: The untapped potential of ascites in ovarian cancer research and treatment . Br J Cancer. 2020, 123:9-16. 10.1038/s41416-020-0875-x 3 . Pericleous M, Sarnowski A, Moore A, Fijten R, Zaman M: The clinical management of abdominal ascites, spontaneous bacterial peritonitis and hepatorenal syndrome: a review of current guidelines and recommendations . Eur J Gastroenterol Hepatol. 2016, 28:e10-8. 10.1097/MEG.0000000000000548 4 . Greenberger, N.J: Ascites & spontaneous bacterial peritonitis . CURRENT Diagnosis & Treatment: Gastroenterology, Hepatology, & Endoscopy, Second Edition. McGraw-Hill, New York; 2012. 515. 5 . Urrunaga NH, Singal AG, Cuthbert JA, Rockey DC: Hemorrhagic ascites. Clinical presentation and outcomes in patients with cirrhosis . J Hepatol. 2013, 58:1113-8. 10.1016/j.jhep.2013.01.015 6 . Ayantunde AA, Parsons SL: Pattern and prognostic factors in patients with malignant ascites: a retrospective study . Ann Oncol. 2007, 18:945-9. 10.1093/annonc/mdl499 7 . Yaguchi A, Ban K, Koshida Y, et al.: Pseudo-Meigs syndrome caused by a giant uterine leiomyoma with cystic degeneration: a case report . J Nippon Med Sch. 2020, 87:80-6. 10.1272/jnms.JNMS.2020_87-205 8 . Giudice LC, Kao LC: Endometriosis . Lancet. 2004, 364:1789-99. 10.1016/S0140-6736(04)17403-5 9 . Machairiotis N, Stylianaki A, Dryllis G, et al.: Extrapelvic endometriosis: a rare entity or an under diagnosed condition? . Diagn Pathol. 2013, 8:194. 10.1186/1746-1596-8-194 10 . Liberati A, Altman DG, Tetzlaff J, et al.: The PRISMA statement for reporting systematic reviews and meta- analyses of studies that evaluate healthcare interventions: explanation and elaboration . BMJ. 2009, 339:b2700. 10.1136/bmj.b2700 11 . Murad MH, Sultan S, Haffar S, Bazerbachi F: Methodological quality and synthesis of case series and case reports . BMJ Evid Based Med. 2018, 23:60-3. 10.1136/bmjebm-2017-110853 12 . Bhojawala J, Heller DS, Cracchiolo B, Sama J: Endometriosis presenting as bloody pleural effusion and ascites-report of a case and review of the literature . Arch Gynecol Obstet. 2000, 264:39-41. 10.1007/pl00007484 13 . Dias CC, Andrade JM, Ferriani RA, et al.: Hemorrhagic ascites associated with endometriosis. A case report . The Journal of Reproductive Medicine. 2000, 45:688-690. 14 . Cheong EC, Lim DT: Massive ascites--an uncommon presentation of endometriosis . Singapore Med J. 2003, 44:98-100. 15 . Goumenou A, Matalliotakis I, Mahutte N, Koumantakis E: Endometriosis mimicking advanced ovarian cancer . Fertil Steril. 2006, 86:219.e23-5. 10.1016/j.fertnstert.2005.12.044 16 . Alabi C, Evbuomwan I, Attwood S, Brady J: Recurrent haemorrhagic ascites secondary to endometriosis: case report . Gynecol Surg. 2007, 4:285-7. 10.1007/s10397-007-0282-9 17 . Palayekar M, Jenci J, Carlson JA Jr: Recurrent hemorrhagic ascites: a rare presentation of endometriosis . Obstet Gynecol. 2007, 110:521-2. 10.1097/01.AOG.0000268283.99315.58 18 . Santos VM, Barbosa ER Jr, Lima SH, Porto AS: Abdominal cocoon associated with endometriosis . Singapore Med J. 2007, 48:e240-2. 19 . Sait KH: Massive ascites as a presentation in a young woman with endometriosis: a case report . Fertil Steril. 2008, 90:2015.e17-9. 10.1016/j.fertnstert.2008.07.021 20 . Ussia A, Betsas G, Corona R, De Cicco C, Koninckx PR: Pathophysiology of cyclic hemorrhagic ascites and endometriosis . J Minim Invasive Gynecol. 2008, 15:677-81. 10.1016/j.jmig.2008.08.012 21 . Day T, Hui K, Perkins S, Pelletier P: Ascites and ileus due to endometriosis: a conservative management approach . Female Pelvic Medicine & Reconstructive Surgery. 2009, 15:471-5. 10.1097/spv.0b013e3181c6e90b 22 . Lin JN, Lin HL, Huang CK, Lai CH, Chung HC, Liang SH, Lin HH: Endometriosis presenting as bloody ascites and shock . J Emerg Med. 2010, 38:30-2. 10.1016/j.jemermed.2008.03.031 23 . Suchetha S, Rema P, Mathew AP, Sebastian P: Endometriosis with massive hemorrhagic ascites . Indian J Cancer. 2010, 47:224-5. 10.4103/0019-509X.63004 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 11 of 13 24 . Shabeerali TU, Rajan R, Kuruvilla AP, et al.: Hemorrhagic ascites: are we missing endometriosis? . Indian J Gastroenterol. 2012, 31:195-7. 10.1007/s12664-012-0221-1 25 . Fernandes LF, Podgaec S, Cotti GC, Abrao MS: Severe endometriosis may be considered in the differential diagnosis in young women presenting massive hemorrhagic ascites . Gynecol Surg. 2011, 8:459. 10.1007/s10397-011-0690-8 26 . Morgan TL, Tomich EB, Heiner JD: Endometriosis presenting with hemorrhagic ascites, severe anemia, and shock . Am J Emerg Med. 2013, 31:272.e1-3. 10.1016/j.ajem.2012.05.008 27 . Mumtahana F, Jiao J, Baoxia CA: Case report: a rare presentation of endometriosis with recurrent massive hemorrhagic ascites which can mislead . Int J Womens Health Reprod Sci. 2014, 2:144-8. 28 . Appleby R, Saroya H, Postgate A, Meer Z: A young woman with abdominal distension . BMJ Case Rep. 2014, 2014: 10.1136/bcr-2014-203726 29 . Asano R, Nakazawa T, Hirahara F, Sakakibara H: Dienogest was effective in treating hemorrhagic ascites caused by endometriosis: a case report . J Minim Invasive Gynecol. 2014, 21:1110-2. 10.1016/j.jmig.2014.04.014 30 . Bignall J, Arambage K, Vimplis S: Endometriosis: a rare and interesting cause of recurrent haemorrhagic ascites . BMJ Case Rep. 2014, 2014: 10.1136/bcr-2013-010052 31 . Cosma S, Ceccaroni M, Benedetto C: A pseudoneoplastic finding of deep endometriosis: laparoscopic triple segmental bowel resection . Wideochir Inne Tech Maloinwazyjne. 2014, 9:463-7. 10.5114/wiitm.2014.41617 32 . Hasdemir PS, Ikiz N, Ozcakir HT, Kara E, Guvenal T: Endometriosis associated with relapsing ascites and pleural effusions . J Obstet Gynaecol. 2015, 35:419. 10.3109/01443615.2014.948823 33 . Hinduja I, Kapadia K, Udwadia F, Bhilawadikar R, Adhe A, Zaveri K: Unusual presentation of endometriosis with haemorrhagic ascites - a case report . J Obstet Gynaecol. 2016, 36:133-4. 10.3109/01443615.2015.1030605 34 . Dun EC, Wong S, Lakhi NA, Nehzat CH: Recurrent massive ascites due to mossy endometriosis . Fertil Steril. 2016, 106:e14. 10.1016/j.fertnstert.2016.07.1119 35 . Pereira N, Gunnala V, Palermo GD, Elias RT: Laparoscopic management of severe endometriosis-related hemorrhagic ascites . J Minim Invasive Gynecol. 2018, 25:8-9. 10.1016/j.jmig.2017.03.010 36 . Magalhães TF, Augusto KL, Mota LP, Costa AR, Puster RA, Bezerra LR: Ascites and encapsulating peritonitis in endometriosis: a systematic review with a case report . Rev Bras Ginecol Obstet. 2018, 40:147-55. 10.1055/s-0038-1626700 37 . Pang L, Shi H, Wang T, et al.: Endometriosis on the surface of the uterus mimicking a malignant tumor: a case report with literature review . Medicine (Baltimore). 2019, 98:e15741. 10.1097/MD.0000000000015741 38 . Wang X, Li Y, Tong J, et al.: Endometriosis presenting with recurrent massive hemorrhagic ascites and diagnosed by core needle biopsy: a case report . Medicine (Baltimore). 2019, 98:e15477. 10.1097/MD.0000000000015477 39 . Gonzalez A, Artazcoz S, Elorriaga F, Timmons D, Carugno J: Endometriosis presenting as recurrent haemorrhagic ascites: a case report and literature review . Int J Fertil Steril. 2020, 14:72-5. 10.22074/ijfs.2020.5895 40 . Setubal A, Sidiropoulou Z, Soares S, Barbosa C: Endometriosis and ascites: a strategy to achieve pregnancy . J Minim Invasive Gynecol. 2015, 22:1104-8. 10.1016/j.jmig.2015.05.013 41 . Kishino F, Inokuchi R, Komaru Y, Takaya N, Yamamoto M, Nakajima S, Yahagi N: A healthy young woman with massive hemorrhagic ascites . Am J Emerg Med. 2015, 33:1841.e1-2. 10.1016/j.ajem.2015.04.039 42 . Soyman Z, Bacanakgil BH, Kaya S, Hasanova M: An uncommon presentation of endometriosis a case report . Int J Reprod Med. 2018, 63:317-8. 43 . Mendes S, Carvalho C, Rodrigues G, Barata S, Calhaz-Jorge C, Osório F: Successful treatment of endometriosis-related hemorrhagic ascites: a report of three cases . Surg Technol Int. 2018, 32:150-5. 44 . Lodha A, Klein T, Elish D, Tarkovsky R: Endometriosis: a rare presentation as hemorrhagic ascites . Pract Gastroenterol. 2008, 32:48-9. 45 . Bean E, Cutner A, Saridogan E, Wong M, Naftalin J, Jurkovic D: Hemoperitoneum as a precursor of deep pelvic endometriosis: prospective cohort study . Ultrasound Obstet Gynecol. 2019, 54:389-94. 10.1002/uog.20222 46 . Rubin J, Rockey DC: Cirrhotic ascites, ovarian carcinoma, and CA-125 . South Med J. 1999, 92:248-50. 10.1097/00007611-199902000-00019 47 . Lockhart CJ, McVeigh GE, Harbinson MT: Elevated CA 125 and ascites: not always malignancy . Ir J Med Sci. 2008, 177:63-6. 10.1007/s11845-007-0070-6 48 . Neighbor ML: Ascites . Emerg Med Clin North Am. 1989, 7:683-97. 49 . Cattau EL Jr, Benjamin SB, Knuff TE, Castell DO: The accuracy of the physical examination in the diagnosis of suspected ascites . JAMA. 1982, 247:1164-6. 50 . Cheng MH, Yen Μ S, Chao KC, Sheu BC, Wang PH: Differential diagnosis of gynecologic organ-related diseases in women presenting with ascites . Taiwan J Obstet Gynecol. 2008, 47:384-90. 10.1016/S1028- 4559(09)60003-6 51 . Su MH, Cho SW, Kung YS, Lin JH, Lee WL, Wang PH: Update on the differential diagnosis of gynecologic organ-related diseases in women presenting with ascites . Taiwan J Obstet Gynecol. 2019, 58:587-91. 10.1016/j.tjog.2019.07.002 52 . Santoro A, Angelico G, Inzani F, et al.: The many faces of endometriosis-related neoplasms in the same patient: a brief report . Gynecol Obstet Invest. 2020, 85:371-6. 10.1159/000508225 53 . Catalina-Fernández I, López-Presa D, Sáenz-Santamaria J: Fine needle aspiration cytology in cutaneous and subcutaneous endometriosis . Acta Cytol. 2007, 51:380-4. 10.1159/000325751 54 . Gungor T, Kanat-Pektas M, Ozat M, Zayifoglu Karaca M: A systematic review: endometriosis presenting with ascites . Arch Gynecol Obstet. 2011, 283:513-8. 10.1007/s00404-010-1664-1 55 . Zeppa P, Vetrani A, Cozzolino I, Palombini L: Endometrial glands in ascites secondary to endometriosis . Diagn Cytopathol. 2004, 30:131-2. 10.1002/dc.10390 56 . Polak G, Barczyński B, Wertel I, et al.: Disrupted iron metabolism in peritoneal fluid may induce oxidative stress in the peritoneal cavity of women with endometriosis . Ann Agric Environ Med. 2018, 25:587-92. 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 12 of 13 10.26444/aaem/75802 57 . Amreen S, Kumar P, Gupta P, Rao P: Evaluation of oxidative stress and severity of endometriosis . J Hum Reprod Sci. 2019, 12:40-6. 10.4103/jhrs.JHRS_27_17 58 . Zhang Z, Zhang M, Li L: Sclerosing encapsulating peritonitis: three case reports and review of the literature . J Int Med Res. 2020, 48:300060520949104. 10.1177/0300060520949104 59 . Bougie O, Healey J, Singh SS: Behind the times: revisiting endometriosis and race . Am J Obstet Gynecol. 2019, 221:35.e1-5. 10.1016/j.ajog.2019.01.238 60 . Bougie O, Yap MI, Sikora L, Flaxman T, Singh S: Influence of race/ethnicity on prevalence and presentation of endometriosis: a systematic review and meta-analysis . BJOG. 2019, 126:1104-15. 10.1111/1471- 0528.15692 61 . Schippert C, Witte Y, Bartels J, Garcia-Rocha GJ, Jentschke M, Hillemanns P, Kundu S: Reproductive capacity and recurrence of disease after surgery for moderate and severe endometriosis - a retrospective single center analysis . BMC Womens Health. 2020, 20:144. 10.1186/s12905-020-01016-3 62 . Zhu Q, Ma J, Zhao X, Liang G, Zhai J, Zhang J: Effects of postoperative medical treatment and expectant treatment on dysmenorrhea after conservative laparoscopic surgery for deep-infiltrating endometriosis accompanied by dysmenorrhea . J Int Med Res. 2020, 48:300060520931666. 10.1177/0300060520931666 2022 Pandraklakis et al. Cureus 14(6): e26222. DOI 10.7759/cureus.26222 13 of 13