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Ovarian cysts and tumors in infancy and childhood

AIM: Review of the clinical presentation, types (histology), and stages of presentation and overall outcome of ovarian tumors. MATERIALS AND METHODS: This is a retrospective study. Forty nine girls from 3 days to 12 years were included in the study. RESULTS: Fourteen girls had benign and thirty thre...

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Autores principales: Mukhopadhyay, Madhumita, Shukla, Ram Mohan, Mukhopadhyay, Biswanath, Mandal, Kartik C., Ray, Amit, Sisodiya, Neha, Patra, Mahadev Prasad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628238/
https://www.ncbi.nlm.nih.gov/pubmed/23599577
http://dx.doi.org/10.4103/0971-9261.107010
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author Mukhopadhyay, Madhumita
Shukla, Ram Mohan
Mukhopadhyay, Biswanath
Mandal, Kartik C.
Ray, Amit
Sisodiya, Neha
Patra, Mahadev Prasad
author_facet Mukhopadhyay, Madhumita
Shukla, Ram Mohan
Mukhopadhyay, Biswanath
Mandal, Kartik C.
Ray, Amit
Sisodiya, Neha
Patra, Mahadev Prasad
author_sort Mukhopadhyay, Madhumita
collection PubMed
description AIM: Review of the clinical presentation, types (histology), and stages of presentation and overall outcome of ovarian tumors. MATERIALS AND METHODS: This is a retrospective study. Forty nine girls from 3 days to 12 years were included in the study. RESULTS: Fourteen girls had benign and thirty three had malignant ovarian tumors. One girl had bilateral ovarian non-Hodgkin lymphoma. Dysgerminoma (40%) was the commonest malignant tumor followed by malignant teratoma (16.6%). CONCLUSION: Pain and abdominal lump are the most common modes of presentation. Prognosis depends on the size of the tumor, stage and histology of the tumor. Conservative surgery should be the aim. Multidisciplinary management gives good prognosis.
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spelling pubmed-36282382013-04-18 Ovarian cysts and tumors in infancy and childhood Mukhopadhyay, Madhumita Shukla, Ram Mohan Mukhopadhyay, Biswanath Mandal, Kartik C. Ray, Amit Sisodiya, Neha Patra, Mahadev Prasad J Indian Assoc Pediatr Surg Original Article AIM: Review of the clinical presentation, types (histology), and stages of presentation and overall outcome of ovarian tumors. MATERIALS AND METHODS: This is a retrospective study. Forty nine girls from 3 days to 12 years were included in the study. RESULTS: Fourteen girls had benign and thirty three had malignant ovarian tumors. One girl had bilateral ovarian non-Hodgkin lymphoma. Dysgerminoma (40%) was the commonest malignant tumor followed by malignant teratoma (16.6%). CONCLUSION: Pain and abdominal lump are the most common modes of presentation. Prognosis depends on the size of the tumor, stage and histology of the tumor. Conservative surgery should be the aim. Multidisciplinary management gives good prognosis. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3628238/ /pubmed/23599577 http://dx.doi.org/10.4103/0971-9261.107010 Text en Copyright: © Journal of Indian Association of Pediatric Surgeons 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
Mukhopadhyay, Madhumita
Shukla, Ram Mohan
Mukhopadhyay, Biswanath
Mandal, Kartik C.
Ray, Amit
Sisodiya, Neha
Patra, Mahadev Prasad
Ovarian cysts and tumors in infancy and childhood
title Ovarian cysts and tumors in infancy and childhood
title_full Ovarian cysts and tumors in infancy and childhood
title_fullStr Ovarian cysts and tumors in infancy and childhood
title_full_unstemmed Ovarian cysts and tumors in infancy and childhood
title_short Ovarian cysts and tumors in infancy and childhood
title_sort ovarian cysts and tumors in infancy and childhood
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628238/
https://www.ncbi.nlm.nih.gov/pubmed/23599577
http://dx.doi.org/10.4103/0971-9261.107010
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