Accessory cavitated uterine malformation (ACUM): A scoping review.
Mullerian anomalies
accessory cavitated uterine malformation
adenomyosis
juvenile cystic adenomyosis
mullerianosis
ultrasound
uterus
Journal
Acta obstetricia et gynecologica Scandinavica
ISSN: 1600-0412
Titre abrégé: Acta Obstet Gynecol Scand
Pays: United States
ID NLM: 0370343
Informations de publication
Date de publication:
12 Feb 2024
12 Feb 2024
Historique:
revised:
09
01
2024
received:
15
09
2023
accepted:
28
01
2024
medline:
12
2
2024
pubmed:
12
2
2024
entrez:
12
2
2024
Statut:
aheadofprint
Résumé
Accessory cavitated uterine malformation (ACUM) is a relatively recent term used to describe a noncommunicating, accessory uterine cavity. ACUM have been published under different terms ranging from juvenile cystic adenomyosis to "uterus-like mass". The objective of this study was to systematically identify all cases of ACUM and definitions described in the literature, regardless of label, and identify morphological, epidemiological, and clinical characteristics as well as management, while also highlighting knowledge gaps. A systematic literature search of three databases was performed, reviewing all records of cystic myometrial lesions. Cases that fitted common definitions for ACUM were included and clinical and imaging characteristics were documented in detail. This work was registered to PROSPERO and reporting followed PRISMA guidelines for scoping reviews. A total of 53 articles were included, comprising 115 cases that met the minimal criteria for ACUM. The median age at onset of symptoms was 17 years, presenting with dysmenorrhea soon after menarche. A total of 19 women were parous. On ultrasound, ACUM appears as unilocular myometrial cysts, usually with ground-glass content. Hemorrhagic content is also observed on magnetic resonance imaging (MRI), with high signal intensity on both T2 and T1-weighted images. Ninety-five (83%) cases were managed surgically, with a trend towards primary nonsurgical options. Although no adverse outcomes were reported, long-term follow-up on subsequent fertility and pregnancy was rare. Despite its increasing recognition as a clinical entity, ACUM often remains underdiagnosed as it shares similarities with other myometrial masses. We propose a unified terminology and definition for ACUM based on the data in this review. ACUM presents as a cavitated lesion, surrounded by a myometrial mantle, in continuity with the anterolateral uterine wall and located beneath the insertion of the round ligament and the interstitial portion of the fallopian tube. In contrast to other uterine abnormalities, a normal uterine cavity is visualized. Future studies are needed, using a clear definition for ACUM, and prospectively investigating management strategies, including long-term follow-up of patient-reported symptoms, fertility, and pregnancy outcomes.
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© 2024 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG).
Références
Grimbizis GF, Di Spiezio SA, Saravelos SH, et al. The Thessaloniki ESHRE/ESGE consensus on diagnosis of female genital anomalies. Hum Reprod. 2016;31:2-7.
Acién P, Acién M, Fernández F, José Mayol M, Aranda I. The cavitated accessory uterine mass: a Müllerian anomaly in women with an otherwise normal uterus. Obstet Gynecol. 2010;116:1101-1109.
Takeuchi H, Kitade M, Kikuchi I, Kumakiri J, Kuroda K, Jinushi M. Diagnosis, laparoscopic management, and histopathologic findings of juvenile cystic adenomyoma: a review of nine cases. Fertil Steril. 2010;94:862-868.
Naftalin J, Bean E, Saridogan E, Barton-Smith P, Arora R, Jurkovic D. Imaging in gynecological disease (21): clinical and ultrasound characteristics of accessory cavitated uterine malformations. Ultrasound Obstet Gynecol. 2021;57:821-828.
Ahmed AA, Swan RW, Owen A, Kraus FT, Patrick F. Uterus-like mass arising in the broad ligament: a metaplasia or Mu ̈ llerian duct anomaly? Case report. Int J Gynecol Pathol. 1997;16:279-281.
Batt RE. Pathogenesis of a parauterine uterus-like mass: developmentally misplaced müllerian tissue-müllerianosis. Fertil Steril. 2010;94:e45.
Batt RE, Smith RA, Buck Louis GM, et al. Müllerianosis. Histol Histopathol. 2007;22:1161-1166.
Zhao CZ, Wang B, Zhong CY, Lu ST, Lei L. Management of uterine cystic adenomyosis by laparoscopic surgery: case report. BMC Womens Health. 2021;21:263.
Fisseha S, Smith YR, Kumetz LM, Mueller GC, Hussain H, Quint EH. Cystic myometrial lesion in the uterus of an adolescent girl. Fertil Steril. 2006;86:716-718.
David C, Burette J, Duminil L, et al. Uterus-like mass: a case report. Eur J Obstet Gynecol Reprod Biol. 2019;233:162-163.
Grimbizis GF, Gordts S, Di Spiezio Sardo A, et al. The ESHRE-ESGE consensus on the classification of female genital tract congenital anomalies. Gynecol Surg. 2013;10:199-212.
Pfeifer SM, Attaran M, Goldstein J, et al. ASRM müllerian anomalies classification 2021. Fertil Steril. 2021;116:1238-1252.
Tricco AC, Lillie E, Zarin W, et al. PRISMA extension for scoping reviews (PRISMA-ScR): checklist and explanation. Ann Intern Med. 2018;169:467-473.
Education and Practical Standards Committee (EFSUMB), European Federation of Societies for Ultrasound in Medicine and Biology. Minimum training recommendations for the practice of medical ultrasound. Ultraschall Med. 2006;27:79-105.
Cozzutto C. Uterus-like mass replacing ovary: report of a new entity. Arch Pathol Lab Med. 1981;105:508-511.
Zhao X, Yang Y. Ultrasound-guided transvaginal aspiration and sclerotherapy for uterine cystic adenomyosis: case report and literature review. Front Med (Lausanne). 2022;9:764523.
Merviel P, Lelievre C, Cambier T, Thomas-Kergastel I, Dupré PF. The first ethanol sclerotherapy of an accessory cavitated uterine mass. Clin Case Reports. 2020;9:19-22.
Minelli F, Agostini A, Siles P, Gnisci A, Pivano A. Treatment of juvenile cystic adenomyoma by sclerotherapy with alcohol instillation: a case report. J Gynecol Obstet Hum Reprod. 2021;50:102081.
Dadhwal V, Sharma A, Khoiwal K. Juvenile cystic adenomyoma mimicking a uterine anomaly: a report of two cases. Eur J Med. 2017;49:59-61.
Nabeshima H, Murakami T, Terada Y, Noda T, Yaegashi N, Okamura K. Total laparoscopic surgery of cystic adenomyoma under hydroultrasonographic monitoring. J Am Assoc Gynecol Laparosc. 2003;10:195-199.
Supermaniam S, Thye WL. Diagnosis and laparoscopic excision of accessory cavitated uterine mass in young women: two case reports. Case Rep Womens Health. 2020;26:e00187.
Stedman TL. Choristoma. Stedman's Medical Dictionary. 28th ed. Lippincott Williams & Wilkins; 2006:371.
Jurkovic D, Gruboeck K, Tailor A, Nicolaides KH. Ultrasound screening for congenital uterine anomalies. Br J Obstet Gynaecol. 1997;104:1320-1321.
Salim R, Woelfer B, Backos M, Regan L, Jurkovic D. Reproducibility of three-dimensional ultrasound diagnosis of congenital uterine anomalies. Ultrasound Obstet Gynecol. 2003;21:578-582.
Chapron C, Tosti C, Marcellin L, et al. Relationship between the magnetic resonance imaging appearance of adenomyosis and endometriosis phenotypes. Hum Reprod. 2017;32:1393-1401.
Kishi Y, Suginami H, Kuramori R, Yabuta M, Suginami R, Taniguchi F. Four subtypes of adenomyosis assessed by magnetic resonance imaging and their specification. Am J Obstet Gynecol. 2012;207(114):e1-e7.
Van den Bosch T, Dueholm M, Leone FP, et al. Terms, definitions and measurements to describe sonographic features of myometrium and uterine masses: a consensus opinion from the morphological uterus sonographic assessment (MUSA) group. Ultrasound Obstet Gynecol. 2015;46:284-298.
García-Tejedor A, Castellarnau M, Ponce J, Fernández ME, Burdio F. Ethanol sclerotherapy of ovarian endometrioma: a safe and effective minimal invasive procedure. Preliminary results. Eur J Obstet Gynecol Reprod Biol. 2015;187:25-29.
Kim GH, Kim PH, Shin JH, Nam IC, Chu HH, Ko HK. Ultrasound-guided sclerotherapy for the treatment of ovarian endometrioma: an updated systematic review and meta-analysis. Eur Radiol. 2022;32:1726-1737.
Xu S, Rao M, Pu Y, Zhou J, Zhang Y. The efficacy of laparoscopic lauromacrogol sclerotherapy in the treatment of simple hepatic cysts located in posterior segments: a refined surgical approach. Ann Palliat Med. 2020;9:3462-3471.
Yalcinkaya TM, Leezer K, Akar ME. Robotic-assisted laparoscopic Management of Juvenile Cystic Adenomyoma: a case report. J Minim Invasive Gynecol. 2010;17(Supplement):S35.
Deblaere L, Froyman W, Van den Bosch T, et al. Juvenile cystic adenomyosis: a case report and review of the literature. Australas J Ultrasound Med. 2019;22:295-300.
Guimarães I, Póvoa AM. Primary dysmenorrhea: assessment and treatment. Rev Bras Ginecol Obstet. 2020;42:501-507.
Mondal R, Bhave P. Accessory cavitated uterine malformation: enhancing awareness about this unexplored perpetrator of dysmenorrhea. Int J Gynaecol Obstet. 2023;162:409-432.
Gupta S, Manchanda S, Vyas S, Malhotra N, Mathur SR, Kulshrestha V. Imaging features of accessory cavitated uterine mass (ACUM): a peculiar yet correctable cause of dysmenorrhea. Abdom Radiol (NY). 2023;48:1100-1106.
Arya S, Burks HR. Juvenile cystic adenomyoma, a rare diagnostic challenge: case reports and literature review. F S Rep. 2021;2:166-171.