Subscribe to RSS

DOI: 10.1055/a-1580-0601
Diagnostic Benefit of the Detection of Mitotic Figures in Endometriotic Lesions
Diagnostischer Vorteil des Nachweises von Mitosefiguren in endometriotischen Läsionen
Abstract
Objectives Endometriosis is a chronic disease which is diagnosed by surgical intervention combined with a histological work-up. Current international and national recommendations do not require the histological determination of the proliferation rate. The diagnostic and clinical importance of the mitotic rate in endometriotic lesions still remains to be elucidated.
Methods In this retrospective study, the mitotic rates and clinical data of 542 patients with histologically diagnosed endometriosis were analyzed. The mean patient age was 33.5 ± 8.0 (17 – 72) years, and the mean reproductive lifespan was 21.2 ± 7.8 (4 – 41) years. Patients were divided into two groups and patientsʼ reproductive history and clinical endometriosis characteristics were compared between groups. The study group consisted of women with confirmed mitotic figures (n = 140, 25.83%) and the control group comprised women without proliferative activity according to their mitotic rates (n = 402, 74.27%).
Results Women with endometriotic lesions and histologically confirmed mitotic figures were significantly more likely to have a higher endometriosis stage (p = 0.001), deep infiltrating endometriosis (p < 0.001), ovarian endometrioma (p = 0.012), and infertility (p = 0.049). A mitotic rate > 0 was seen significantly less often in cases with incidental findings of endometriosis (p = 0.031). The presence of symptoms and basic characteristics such as age, age at onset of menarche, reproductive lifespan and parity did not differ between the group with and the group without mitotic figures.
Conclusion This study shows that a simple histological assessment of the mitotic rate offers additional diagnostic value for the detection of advanced stages of endometriosis. The possible role as a predictive marker for the recurrence of endometriosis or the development of endometriosis-associated cancer will require future study.
Zusammenfassung
Ziele Endometriose ist eine chronische Erkrankung, die durch einen chirurgischen Eingriff und einen histologischen Nachweis diagnostiziert wird. Laut den aktuellen internationalen und nationalen Empfehlungen ist der histologische Nachweis der Proliferationsrate nicht nötig. Die diagnostische und klinische Bedeutung der Mitoserate in endometriotischen Läsionen ist immer noch ungeklärt.
Methoden In dieser retrospektiven Studie wurden die Mitoseraten und die klinischen Daten von 542 Patientinnen mit histologisch nachgewiesener Endometriose analysiert. Das durchschnittliche Alter der Patientinnen betrug 33,5 ± 8,0 (17 – 72) Jahre, und ihre durchschnittliche Reproduktionsspanne lag bei 21,2 ± 7,8 (4 – 41) Jahren. Die Reproduktionsgeschichte und klinischen Endometriosemerkmale wurden verglichen. Die Studiengruppe bestand aus Frauen, bei denen Mitosefiguren nachgewiesen wurden (n = 140, 25,83%), und die Kontrollgruppe bestand aus Frauen ohne Proliferationsaktivität (n = 402, 74,27%).
Ergebnisse Frauen mit endometriotischen Läsionen und einem histologischen Nachweis von Mitosefiguren hatten signifikant häufiger ein klinisch höheres Endometriosestadium (p = 0,001), tief infiltrierende Endometriose (p < 0,001), ovarielle Endometriome (p = 0,012) oder Infertilität (p = 0,049). Frauen, bei denen eine Endometriose als Zufallsbefund entdeckt wurde, hatten signifikant weniger oft eine Mitoserate von > 0 (p = 0,031). Es gab keine Unterschiede in den Symptomen und Charakteristika wie Alter, Menarche, Reproduktionsspanne und Parität zwischen der Gruppe mit und der Gruppe ohne Mitosefiguren.
Schlussfolgerung Diese Studie zeigt, dass eine einfache histologische Evaluierung der Mitoserate für die Erkennung einer Endometriose im fortgeschrittenen Stadium einen diagnostischen Mehrwert bietet. Um die Bedeutung der Mitoserate als prädiktiven Marker für das Wiederauftreten einer Endometriose bzw. für die Entwicklung von endometrioseassoziiertem Krebs zu evaluieren, werden weitere Untersuchungen benötigt.
Key words
endometriosis - mitotic rate - infertility - laparoscopy - endometriosis-associated ovarian cancerSchlüsselwörter
Endometriose - Mitoserate - Infertilität - Laparoskopie - endometrioseassoziiertes OvarialkarzinomPublication History
Received: 22 April 2021
Accepted after revision: 05 August 2021
Article published online:
10 January 2022
© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References
- 1 Giudice LC, Kao LC. Endometriosis. Lancet 2004; 364: 1789-1799
- 2 Nicolaus K, Reckenbeil L, Bräuer D. et al. Cycle-related diarrhea and dysmenorrhea are independent predictors of peritoneal endometriosis, cycle-related dyschezia is an independent predictor of rectal involvement. Geburtshilfe Frauenheilkd 2020; 80: 307-315
- 3 Bjorkman S, Taylor HS. MicroRNAs in endometriosis: biological function and emerging biomarker candidates. Biol Reprod 2019; 100: 1135-1146
- 4 Moustafa S, Burn M, Mamillapalli R. et al. Accurate diagnosis of endometriosis using serum microRNAs. Am J Obstet Gynecol 2020; 22: 557.e1-557.e11
- 5 Dunselman GA, Vermeulen N, Becker C. et al. European Society of Human Reproduction and Embryology. ESHRE guideline: management of women with endometriosis. Hum Reprod 2014; 29: 400-412
- 6 Burghaus S, Schäfer SD, Beckmann MW. et al. Diagnosis and Treatment of Endometriosis. Guideline of the DGGG, SGGG and OEGGG (S2k Level, AWMF Registry Number 015/045, August 2020). Geburtshilfe Frauenheilkd 2021; 81: 422-446
- 7 Zeppernick F, Zeppernick M, Janschek E. et al. for the QS Endo Working Group of the Endometriosis Research Foundation (SEF). QS ENDO Real – A Study by the German Endometriosis Research Foundation (SEF) on the Reality of Care for Patients with Endometriosis in Germany, Austria and Switzerland. Geburtshilfe Frauenheilkd 2020; 80: 179-189
- 8 Nisolle-Pochet M, Casanas-Roux F, Donnez J. Histologic study of ovarian endometriosis after hormonal therapy. Fertil Steril 1988; 49: 423-426
- 9 Nisolle M, Casanas-Roux F, Anaf V. et al. Morphometric study of the stromal vascularization in peritoneal endometriosis. Fertil Steril 1993; 59: 681-684
- 10 Yadav KS, Gonuguntla S, Ealla KK. et al. Assessment of interobserver variability in mitotic figure counting in different histological grades of oral squamous cell carcinoma. J Contemp Dent Pract 2012; 13: 339-344
- 11 Barry M, Sinha SK, Leader MB. et al. Poor agreement in recognition of abnormal mitoses: requirement for standardized and robust definitions. Histopathology 2001; 38: 68-72
- 12 Kahyaoglu I, Kahyaoglu S, Moraloglu O. et al. Comparison of Ki-67 proliferative index between eutopic and ectopic endometrium: a case control study. Taiwan J Obstet Gynecol 2012; 51: 393-396
- 13 Fukunaga M, Nomura K, Ishikawa E. et al. Ovarian atypical endometriosis: its close association with malignant epithelial tumours. Histopathology 1997; 30: 249-255
- 14 DeAngelo C, Tarasiewicz MB, Strother A. et al. Endometriosis: A malignant fingerprint. J Cancer Res Ther Oncol 2020; 8: 206
- 15 Revised American Society for Reproductive Medicine classification of endometriosis: 1996. Fertil Steril 1997; 67: 817-821
- 16 Haas D, Chvatal R, Habelsberger A. et al. Preoperative planning of surgery for deeply infiltrating endometriosis using the ENZIAN classification. Eur J Obstet Gynecol Reprod Biol 2013; 166: 99-103
- 17 Nisolle M, Casanas-Roux F, Donnez J. Immunohistochemical analysis of proliferative activity and steroid receptor expression in peritoneal and ovarian endometriosis. Fertil Steril 1997; 68: 912-919
- 18 Louis D, Ohgaki H, Wiestler O, Cavenee W. eds. WHO Classification of Tumours of the central nervous System. 4th ed. Lyon: WHO Press; 2016
- 19 Sinaii N, Plumb K, Cotton L. et al. Differences in characteristics among 1,000 women with endometriosis based on extent of disease. Fertil Steril 2008; 89: 538-545
- 20 Abbas S, Ihle P, Köster I. et al. Prevalence and incidence of diagnosed endometriosis and risk of endometriosis in patients with endometriosis-related symptoms: findings from a statutory health insurance-based cohort in Germany. Eur J Obstet Gynecol Reprod Biol 2012; 160: 79-83
- 21 Fauconnier A, Chapron C, Dubuisson J-B. et al. Relation between pain symptoms and the anatomic location of deep infiltrating endometriosis. Fertil Steril 2002; 78: 719-726
- 22 Kho RM, Andres MP, Borrelli GM. et al. Surgical treatment of different types of endometriosis: Comparison of major society guidelines and preferred clinical algorithms. Best Pract Res Clin Obstet Gynaecol 2018; 51: 102-110
- 23 Vercellini P, Fedele L, Aimi G. et al. Association between endometriosis stage, lesion type, patient characteristics and severity of pelvic pain symptoms: a multivariate analysis of over 1000 patients. Hum Reprod 2007; 22: 266-271
- 24 Wimberger P, Grübling N, Riehn A. et al. Endometriosis – A Chameleon: Patientsʼ Perception of Clinical Symptoms, Treatment Strategies and Their Impact on Symptoms. Geburtshilfe Frauenheilkd 2014; 74: 940-946
- 25 Nepomnyashchikh LM, Lushnikova EL, Molodykh OP. et al. Immunocytochemical analysis of proliferative activity of endometrial and myometrial cell populations in focal and stromal adenomyosis. Bull Exp Biol Med 2013; 155: 512-517
- 26 Audebert A, Petousis S, Margioula-Siarkou C. et al. Anatomic distribution of endometriosis: A reappraisal based on series of 1101 patients. Eur J Obstet Gynecol Reprod Biol 2018; 230: 36-40
- 27 Findeklee S, Radosa JC, Hamza A. et al. Treatment algorithm for women with endometriosis in a certified Endometriosis Unit. Minerva Ginecol 2020; 72: 43-49
- 28 Bulun SE, Wan Y, Matei D. Epithelial Mutations in Endometriosis: Link to Ovarian Cancer. Endocrinology 2019; 160: 626-638