Cargando…
Ovarian Granulosa Cell Tumor: Clinical Features, Treatment, Outcome, and Prognostic Factors
BACKGROUND: Granulosa cell tumors are rare neoplasms characterized by long natural history and favorable prognosis. AIMS: The objective of this study was to determine the clinical presentation, treatment, outcome, and prognostic factors for patients of granulosa cell tumors. MATERIALS AND METHODS: A...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978936/ https://www.ncbi.nlm.nih.gov/pubmed/24741552 http://dx.doi.org/10.4103/1947-2714.128475 |
_version_ | 1782310654137335808 |
---|---|
author | Khosla, Divya Dimri, Kislay Pandey, Awadhesh K. Mahajan, Rohit Trehan, Romeeta |
author_facet | Khosla, Divya Dimri, Kislay Pandey, Awadhesh K. Mahajan, Rohit Trehan, Romeeta |
author_sort | Khosla, Divya |
collection | PubMed |
description | BACKGROUND: Granulosa cell tumors are rare neoplasms characterized by long natural history and favorable prognosis. AIMS: The objective of this study was to determine the clinical presentation, treatment, outcome, and prognostic factors for patients of granulosa cell tumors. MATERIALS AND METHODS: A retrospective analysis of 26 patients of granulosa cell tumor of ovary from 2002 to 2011 was carried out. The records of all patients were analyzed to determine clinical presentation, treatment, survival, and prognostic factors. RESULTS: The median age of the patients was 50 years (range, 17-71 years). Abdominal pain was the most common presenting symptom. The median follow-up was 71.4 months (range, 21.6-149.9 months). The estimated 5 and 10 year overall survival (OS) was 84.6 and 72.5%, respectively. Event-free survival (EFS) was 76.5 and 52.9% at 5 and 10 years, respectively. Advanced stage was significant independent poor prognostic indicator for both OS and EFS. CONCLUSION: Majority of the patients with granulosa cell tumors of the ovary present in early stage. Surgery is the primary treatment modality for granulosa cell tumors. Advanced stage and presence of residual disease were associated with inferior survival, but only prospective studies can ascertain their definite role. |
format | Online Article Text |
id | pubmed-3978936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39789362014-04-16 Ovarian Granulosa Cell Tumor: Clinical Features, Treatment, Outcome, and Prognostic Factors Khosla, Divya Dimri, Kislay Pandey, Awadhesh K. Mahajan, Rohit Trehan, Romeeta N Am J Med Sci Original Article BACKGROUND: Granulosa cell tumors are rare neoplasms characterized by long natural history and favorable prognosis. AIMS: The objective of this study was to determine the clinical presentation, treatment, outcome, and prognostic factors for patients of granulosa cell tumors. MATERIALS AND METHODS: A retrospective analysis of 26 patients of granulosa cell tumor of ovary from 2002 to 2011 was carried out. The records of all patients were analyzed to determine clinical presentation, treatment, survival, and prognostic factors. RESULTS: The median age of the patients was 50 years (range, 17-71 years). Abdominal pain was the most common presenting symptom. The median follow-up was 71.4 months (range, 21.6-149.9 months). The estimated 5 and 10 year overall survival (OS) was 84.6 and 72.5%, respectively. Event-free survival (EFS) was 76.5 and 52.9% at 5 and 10 years, respectively. Advanced stage was significant independent poor prognostic indicator for both OS and EFS. CONCLUSION: Majority of the patients with granulosa cell tumors of the ovary present in early stage. Surgery is the primary treatment modality for granulosa cell tumors. Advanced stage and presence of residual disease were associated with inferior survival, but only prospective studies can ascertain their definite role. Medknow Publications & Media Pvt Ltd 2014-03 /pmc/articles/PMC3978936/ /pubmed/24741552 http://dx.doi.org/10.4103/1947-2714.128475 Text en Copyright: © North American Journal of Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Khosla, Divya Dimri, Kislay Pandey, Awadhesh K. Mahajan, Rohit Trehan, Romeeta Ovarian Granulosa Cell Tumor: Clinical Features, Treatment, Outcome, and Prognostic Factors |
title | Ovarian Granulosa Cell Tumor: Clinical Features, Treatment, Outcome, and Prognostic Factors |
title_full | Ovarian Granulosa Cell Tumor: Clinical Features, Treatment, Outcome, and Prognostic Factors |
title_fullStr | Ovarian Granulosa Cell Tumor: Clinical Features, Treatment, Outcome, and Prognostic Factors |
title_full_unstemmed | Ovarian Granulosa Cell Tumor: Clinical Features, Treatment, Outcome, and Prognostic Factors |
title_short | Ovarian Granulosa Cell Tumor: Clinical Features, Treatment, Outcome, and Prognostic Factors |
title_sort | ovarian granulosa cell tumor: clinical features, treatment, outcome, and prognostic factors |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978936/ https://www.ncbi.nlm.nih.gov/pubmed/24741552 http://dx.doi.org/10.4103/1947-2714.128475 |
work_keys_str_mv | AT khosladivya ovariangranulosacelltumorclinicalfeaturestreatmentoutcomeandprognosticfactors AT dimrikislay ovariangranulosacelltumorclinicalfeaturestreatmentoutcomeandprognosticfactors AT pandeyawadheshk ovariangranulosacelltumorclinicalfeaturestreatmentoutcomeandprognosticfactors AT mahajanrohit ovariangranulosacelltumorclinicalfeaturestreatmentoutcomeandprognosticfactors AT trehanromeeta ovariangranulosacelltumorclinicalfeaturestreatmentoutcomeandprognosticfactors |