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A rare case of uterine leiomyosarcoma: a case report
INTRODUCTION: Malignant change in a leiomyoma or uterine fibroid is termed leiomyosarcoma. It arises from smooth muscle of the uterus and is a rare tumor that accounts for 2% to 5% of all uterine malignancies. Very few cases are reported in the literature. Our patient did not have any history of gen...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2917442/ https://www.ncbi.nlm.nih.gov/pubmed/20649999 http://dx.doi.org/10.1186/1752-1947-4-222 |
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author | Vellanki, Venkata Sujatha Rao, Meghana Sunkavalli, Chinna Babu Chinamotu, Rao N Kaja, Shailaja |
author_facet | Vellanki, Venkata Sujatha Rao, Meghana Sunkavalli, Chinna Babu Chinamotu, Rao N Kaja, Shailaja |
author_sort | Vellanki, Venkata Sujatha |
collection | PubMed |
description | INTRODUCTION: Malignant change in a leiomyoma or uterine fibroid is termed leiomyosarcoma. It arises from smooth muscle of the uterus and is a rare tumor that accounts for 2% to 5% of all uterine malignancies. Very few cases are reported in the literature. Our patient did not have any history of genital bleeding, which is the usual presentation in uterine sarcoma. We report an original case report of an unusual presentation of this rare tumor arising from the uterus. CASE PRESENTATION: A 40-year-old nulliparous woman of South Indian origin presented with a mass in her abdomen for one year with a rapid increase in size over the previous three months. Tumor marker CA-125 was raised, and a computed tomography scan showed a mass arising from the pelvis. An exploratory laparotomy was performed and the histopathology report confirmed the diagnosis of uterine leiomyosarcoma. CONCLUSION: Because of their rarity, uterine sarcomas are not suitable for screening. Diagnosis is by histopathologic examination and surgery is the only treatment. The prognosis for women with uterine sarcoma primarily depends on the extent of disease at the time of diagnosis and the mitotic index. |
format | Text |
id | pubmed-2917442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29174422010-08-07 A rare case of uterine leiomyosarcoma: a case report Vellanki, Venkata Sujatha Rao, Meghana Sunkavalli, Chinna Babu Chinamotu, Rao N Kaja, Shailaja J Med Case Reports Case Report INTRODUCTION: Malignant change in a leiomyoma or uterine fibroid is termed leiomyosarcoma. It arises from smooth muscle of the uterus and is a rare tumor that accounts for 2% to 5% of all uterine malignancies. Very few cases are reported in the literature. Our patient did not have any history of genital bleeding, which is the usual presentation in uterine sarcoma. We report an original case report of an unusual presentation of this rare tumor arising from the uterus. CASE PRESENTATION: A 40-year-old nulliparous woman of South Indian origin presented with a mass in her abdomen for one year with a rapid increase in size over the previous three months. Tumor marker CA-125 was raised, and a computed tomography scan showed a mass arising from the pelvis. An exploratory laparotomy was performed and the histopathology report confirmed the diagnosis of uterine leiomyosarcoma. CONCLUSION: Because of their rarity, uterine sarcomas are not suitable for screening. Diagnosis is by histopathologic examination and surgery is the only treatment. The prognosis for women with uterine sarcoma primarily depends on the extent of disease at the time of diagnosis and the mitotic index. BioMed Central 2010-07-22 /pmc/articles/PMC2917442/ /pubmed/20649999 http://dx.doi.org/10.1186/1752-1947-4-222 Text en Copyright ©2010 Vellanki et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Vellanki, Venkata Sujatha Rao, Meghana Sunkavalli, Chinna Babu Chinamotu, Rao N Kaja, Shailaja A rare case of uterine leiomyosarcoma: a case report |
title | A rare case of uterine leiomyosarcoma: a case report |
title_full | A rare case of uterine leiomyosarcoma: a case report |
title_fullStr | A rare case of uterine leiomyosarcoma: a case report |
title_full_unstemmed | A rare case of uterine leiomyosarcoma: a case report |
title_short | A rare case of uterine leiomyosarcoma: a case report |
title_sort | rare case of uterine leiomyosarcoma: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2917442/ https://www.ncbi.nlm.nih.gov/pubmed/20649999 http://dx.doi.org/10.1186/1752-1947-4-222 |
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