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Vaginal leiomyoma mimicking a Cystocele (report case)
INTRODUCTION AND IMPORTANCE: Leiomyoma, known as a disease of the uterus, composed of spindle-shaped smooth muscle fibers and collagenous stroma, is rarely encountered in other sites especially in the vagina. CASE PRESENTATION: We report, here, an exceptional case of a vaginal leiomyoma situated in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968001/ https://www.ncbi.nlm.nih.gov/pubmed/35364392 http://dx.doi.org/10.1016/j.ijscr.2022.106955 |
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author | Touimi Benjelloun, Ahmed Ziad, Imane Elkaroini, Douha Boufettal, Houssine Mahdaoui, Sakher Samouh, Naima |
author_facet | Touimi Benjelloun, Ahmed Ziad, Imane Elkaroini, Douha Boufettal, Houssine Mahdaoui, Sakher Samouh, Naima |
author_sort | Touimi Benjelloun, Ahmed |
collection | PubMed |
description | INTRODUCTION AND IMPORTANCE: Leiomyoma, known as a disease of the uterus, composed of spindle-shaped smooth muscle fibers and collagenous stroma, is rarely encountered in other sites especially in the vagina. CASE PRESENTATION: We report, here, an exceptional case of a vaginal leiomyoma situated in the anterior vaginal wall suggesting in the first place a cystocele. The MRI objectified a rounded formation of the anterior wall of the vagina with regular contours highly suggestive of a vaginal leimyoma. The tumor was surgically removed by the vaginal route. The histopathologic examination confirmed the diagnosis of vaginal leiomyoma. CLINICAL DISCUSSION: Vaginal leiomyomas are commonly seen in women between the ages of 35 and 50 and are believed to be more common in Caucasian women. Although a rare tumor, vaginal leiomyomas may present with a variety of clinical features and may be mistaken preoperatively for a cystocele, urethrocele, Skene's duct abscess, Gartner's duct cysts, urethral diverticulum, vaginal cysts, cysts Bartholin's gland or a malignant vaginal tumor. The diagnosis is based on careful examination and preoperative imaging (ultrasonography and MRI). Removal of the tumor by vaginal route, wherever possible, with subsequent histopathological examination appears to be the optimum management plan. Although the lesion is benign, local recurrences following incomplete resection and sarcomatous changes have been reported. CONCLUSION: Vaginal leiomyoma is a rare benign tumor. The diagnosis is often made only postoperatively after resection of the mass. The tumors may be found in any location within the vagina but are most commonly located on an anterior wall. Imaging can confirm the vaginal origin of the lesion. Surgical excision is the treatment of choice. The diagnosis is based on the histological study of the tumor. |
format | Online Article Text |
id | pubmed-8968001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-89680012022-04-01 Vaginal leiomyoma mimicking a Cystocele (report case) Touimi Benjelloun, Ahmed Ziad, Imane Elkaroini, Douha Boufettal, Houssine Mahdaoui, Sakher Samouh, Naima Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Leiomyoma, known as a disease of the uterus, composed of spindle-shaped smooth muscle fibers and collagenous stroma, is rarely encountered in other sites especially in the vagina. CASE PRESENTATION: We report, here, an exceptional case of a vaginal leiomyoma situated in the anterior vaginal wall suggesting in the first place a cystocele. The MRI objectified a rounded formation of the anterior wall of the vagina with regular contours highly suggestive of a vaginal leimyoma. The tumor was surgically removed by the vaginal route. The histopathologic examination confirmed the diagnosis of vaginal leiomyoma. CLINICAL DISCUSSION: Vaginal leiomyomas are commonly seen in women between the ages of 35 and 50 and are believed to be more common in Caucasian women. Although a rare tumor, vaginal leiomyomas may present with a variety of clinical features and may be mistaken preoperatively for a cystocele, urethrocele, Skene's duct abscess, Gartner's duct cysts, urethral diverticulum, vaginal cysts, cysts Bartholin's gland or a malignant vaginal tumor. The diagnosis is based on careful examination and preoperative imaging (ultrasonography and MRI). Removal of the tumor by vaginal route, wherever possible, with subsequent histopathological examination appears to be the optimum management plan. Although the lesion is benign, local recurrences following incomplete resection and sarcomatous changes have been reported. CONCLUSION: Vaginal leiomyoma is a rare benign tumor. The diagnosis is often made only postoperatively after resection of the mass. The tumors may be found in any location within the vagina but are most commonly located on an anterior wall. Imaging can confirm the vaginal origin of the lesion. Surgical excision is the treatment of choice. The diagnosis is based on the histological study of the tumor. Elsevier 2022-03-19 /pmc/articles/PMC8968001/ /pubmed/35364392 http://dx.doi.org/10.1016/j.ijscr.2022.106955 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Touimi Benjelloun, Ahmed Ziad, Imane Elkaroini, Douha Boufettal, Houssine Mahdaoui, Sakher Samouh, Naima Vaginal leiomyoma mimicking a Cystocele (report case) |
title | Vaginal leiomyoma mimicking a Cystocele (report case) |
title_full | Vaginal leiomyoma mimicking a Cystocele (report case) |
title_fullStr | Vaginal leiomyoma mimicking a Cystocele (report case) |
title_full_unstemmed | Vaginal leiomyoma mimicking a Cystocele (report case) |
title_short | Vaginal leiomyoma mimicking a Cystocele (report case) |
title_sort | vaginal leiomyoma mimicking a cystocele (report case) |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968001/ https://www.ncbi.nlm.nih.gov/pubmed/35364392 http://dx.doi.org/10.1016/j.ijscr.2022.106955 |
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