Epididymal adenomatoid tumor: a case report and literature review

Abstract Background Adenomatoid tumor is a very rare benign neoplasm of mesothelial origin affecting mainly female and male genital tracts. The diagnosis is challenging as this tumor mimics many differential diagnoses. The current literature offers only some case reports and short series of adenomat...

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Main Authors: Boubacar Efared, Idrissa Boubacar, Djibo Soumana, Aïchatou Balaraba Abani Bako, Idrissa Seriba Coulibaly, Hamadou Halidou Koura, Habiba Salifou Boureima, Hassan Nouhou
Format: Article
Language:English
Published: SpringerOpen 2022-11-01
Series:African Journal of Urology
Subjects:
Online Access:https://doi.org/10.1186/s12301-022-00329-z
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author Boubacar Efared
Idrissa Boubacar
Djibo Soumana
Aïchatou Balaraba Abani Bako
Idrissa Seriba Coulibaly
Hamadou Halidou Koura
Habiba Salifou Boureima
Hassan Nouhou
author_facet Boubacar Efared
Idrissa Boubacar
Djibo Soumana
Aïchatou Balaraba Abani Bako
Idrissa Seriba Coulibaly
Hamadou Halidou Koura
Habiba Salifou Boureima
Hassan Nouhou
author_sort Boubacar Efared
collection DOAJ
description Abstract Background Adenomatoid tumor is a very rare benign neoplasm of mesothelial origin affecting mainly female and male genital tracts. The diagnosis is challenging as this tumor mimics many differential diagnoses. The current literature offers only some case reports and short series of adenomatoid tumors. Case presentation A 47-year-old patient with unremarkable medical history presented for chronic mild pain of the right testis evolving for months. The physical examination shows a palpable right intrascrotal nodule of 10 mm in greatest diameter. The nodule was painful, mobile with firm consistency. The laboratory investigations were within normal limits, the scrotal ultrasonography showed a well-circumscribed predominantly hyperechoic intrascrotal nodule in the right epididymal head with heterogeneous echostructure. Excisional biopsy of the lesion was performed and the histopathological analysis showed a well-circumscribed tumor with microcystic and trabecular architecture made of small interconnected tubules and cysts lined by flattened cells with prominent vacuolization and thread-like bridging strands, consistent with an epididymal adenomatoid tumor. The postoperative course was uneventful and the patient was discharged. Four months after surgical treatment, the patient has no sign of the disease. Conclusion Testicular adenomatoid tumors are uncommon benign neoplasms with diagnostic challenge. Adenomatoid tumors arising in epididymis are managed by excisional biopsy with testis-sparing surgery avoiding unnecessary orchidectomy.
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spelling doaj.art-eca4a7d0e27e4956a7da1d5731bb00632022-12-22T02:55:07ZengSpringerOpenAfrican Journal of Urology1110-57041961-99872022-11-012811610.1186/s12301-022-00329-zEpididymal adenomatoid tumor: a case report and literature reviewBoubacar Efared0Idrissa Boubacar1Djibo Soumana2Aïchatou Balaraba Abani Bako3Idrissa Seriba Coulibaly4Hamadou Halidou Koura5Habiba Salifou Boureima6Hassan Nouhou7Faculty of Health Sciences, Abdou Moumouni UniversityPathology Laboratory, Niamey National HospitalGeneral Referral HospitalFaculty of Health Sciences, Abdou Moumouni UniversityGeneral Referral HospitalGeneral Referral HospitalGeneral Referral HospitalFaculty of Health Sciences, Abdou Moumouni UniversityAbstract Background Adenomatoid tumor is a very rare benign neoplasm of mesothelial origin affecting mainly female and male genital tracts. The diagnosis is challenging as this tumor mimics many differential diagnoses. The current literature offers only some case reports and short series of adenomatoid tumors. Case presentation A 47-year-old patient with unremarkable medical history presented for chronic mild pain of the right testis evolving for months. The physical examination shows a palpable right intrascrotal nodule of 10 mm in greatest diameter. The nodule was painful, mobile with firm consistency. The laboratory investigations were within normal limits, the scrotal ultrasonography showed a well-circumscribed predominantly hyperechoic intrascrotal nodule in the right epididymal head with heterogeneous echostructure. Excisional biopsy of the lesion was performed and the histopathological analysis showed a well-circumscribed tumor with microcystic and trabecular architecture made of small interconnected tubules and cysts lined by flattened cells with prominent vacuolization and thread-like bridging strands, consistent with an epididymal adenomatoid tumor. The postoperative course was uneventful and the patient was discharged. Four months after surgical treatment, the patient has no sign of the disease. Conclusion Testicular adenomatoid tumors are uncommon benign neoplasms with diagnostic challenge. Adenomatoid tumors arising in epididymis are managed by excisional biopsy with testis-sparing surgery avoiding unnecessary orchidectomy.https://doi.org/10.1186/s12301-022-00329-zTestisEpididymisAdenomatoid tumorHistopathology
spellingShingle Boubacar Efared
Idrissa Boubacar
Djibo Soumana
Aïchatou Balaraba Abani Bako
Idrissa Seriba Coulibaly
Hamadou Halidou Koura
Habiba Salifou Boureima
Hassan Nouhou
Epididymal adenomatoid tumor: a case report and literature review
African Journal of Urology
Testis
Epididymis
Adenomatoid tumor
Histopathology
title Epididymal adenomatoid tumor: a case report and literature review
title_full Epididymal adenomatoid tumor: a case report and literature review
title_fullStr Epididymal adenomatoid tumor: a case report and literature review
title_full_unstemmed Epididymal adenomatoid tumor: a case report and literature review
title_short Epididymal adenomatoid tumor: a case report and literature review
title_sort epididymal adenomatoid tumor a case report and literature review
topic Testis
Epididymis
Adenomatoid tumor
Histopathology
url https://doi.org/10.1186/s12301-022-00329-z
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AT idrissaseribacoulibaly epididymaladenomatoidtumoracasereportandliteraturereview
AT hamadouhalidoukoura epididymaladenomatoidtumoracasereportandliteraturereview
AT habibasalifouboureima epididymaladenomatoidtumoracasereportandliteraturereview
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