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Clinicopathological correlation of choroidal melanoma in Indian population: A study of 113 cases
AIM: To correlate the clinical presentation, tumor characteristics, and histopathological findings of choroidal melanoma in the Indian population MATERIALS AND METHODS: A retrospective analysis of 113 patients of choroidal melanoma over a period of 10 years was done. Patient demography, clinical pre...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339674/ https://www.ncbi.nlm.nih.gov/pubmed/22557876 http://dx.doi.org/10.4103/0974-620X.94766 |
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author | Dhupper, Maneesh Biswas, Jyotirmay Gopal, Lingam Kumar, S. Krishna Khetan, Vikas |
author_facet | Dhupper, Maneesh Biswas, Jyotirmay Gopal, Lingam Kumar, S. Krishna Khetan, Vikas |
author_sort | Dhupper, Maneesh |
collection | PubMed |
description | AIM: To correlate the clinical presentation, tumor characteristics, and histopathological findings of choroidal melanoma in the Indian population MATERIALS AND METHODS: A retrospective analysis of 113 patients of choroidal melanoma over a period of 10 years was done. Patient demography, clinical presentation, tumor characteristics, and histopathological findings were correlated. RESULTS: Among 113 patients histopathologically diagnosed with choroidal melanoma over 10 years, most were males. The mean age was 45.9 ± 14.84 years among which 6 (5.3%) patients were less than 20 years. Thirty-six (31.8%) patients were misdiagnosed. The mean basal diameter was 12.41 ± 1.4 mm. Mixed cell type was seen in 71 (63%) patients, while 28 (25%) patients had spindle cell type. Epithelioid cell type was present in 11 (10%) patients and necrotic cell type was seen in 3 (2%) patients. Enucleation was the primary treatment modality in 107 (94.6%) patients, while exenteration was done in 6 (5.3%) patients. Three patients with epithelioid cell type with orbital extension underwent exenteration. The mean follow-up period was 14 months. No mortality was reported at the end of 5 years in patients with longer follow-up. CONCLUSIONS: Malignant melanoma of the choroid is a rare occurrence. They can occur in younger age group and can be misdiagnosed. Mixed cell type is commonest. Diffuse tumors with epithelioid cell type are likely to have orbital extension. |
format | Online Article Text |
id | pubmed-3339674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33396742012-05-03 Clinicopathological correlation of choroidal melanoma in Indian population: A study of 113 cases Dhupper, Maneesh Biswas, Jyotirmay Gopal, Lingam Kumar, S. Krishna Khetan, Vikas Oman J Ophthalmol Original Article AIM: To correlate the clinical presentation, tumor characteristics, and histopathological findings of choroidal melanoma in the Indian population MATERIALS AND METHODS: A retrospective analysis of 113 patients of choroidal melanoma over a period of 10 years was done. Patient demography, clinical presentation, tumor characteristics, and histopathological findings were correlated. RESULTS: Among 113 patients histopathologically diagnosed with choroidal melanoma over 10 years, most were males. The mean age was 45.9 ± 14.84 years among which 6 (5.3%) patients were less than 20 years. Thirty-six (31.8%) patients were misdiagnosed. The mean basal diameter was 12.41 ± 1.4 mm. Mixed cell type was seen in 71 (63%) patients, while 28 (25%) patients had spindle cell type. Epithelioid cell type was present in 11 (10%) patients and necrotic cell type was seen in 3 (2%) patients. Enucleation was the primary treatment modality in 107 (94.6%) patients, while exenteration was done in 6 (5.3%) patients. Three patients with epithelioid cell type with orbital extension underwent exenteration. The mean follow-up period was 14 months. No mortality was reported at the end of 5 years in patients with longer follow-up. CONCLUSIONS: Malignant melanoma of the choroid is a rare occurrence. They can occur in younger age group and can be misdiagnosed. Mixed cell type is commonest. Diffuse tumors with epithelioid cell type are likely to have orbital extension. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3339674/ /pubmed/22557876 http://dx.doi.org/10.4103/0974-620X.94766 Text en Copyright: © 2012 Dhupper M, et al http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Original Article Dhupper, Maneesh Biswas, Jyotirmay Gopal, Lingam Kumar, S. Krishna Khetan, Vikas Clinicopathological correlation of choroidal melanoma in Indian population: A study of 113 cases |
title | Clinicopathological correlation of choroidal melanoma in Indian population: A study of 113 cases |
title_full | Clinicopathological correlation of choroidal melanoma in Indian population: A study of 113 cases |
title_fullStr | Clinicopathological correlation of choroidal melanoma in Indian population: A study of 113 cases |
title_full_unstemmed | Clinicopathological correlation of choroidal melanoma in Indian population: A study of 113 cases |
title_short | Clinicopathological correlation of choroidal melanoma in Indian population: A study of 113 cases |
title_sort | clinicopathological correlation of choroidal melanoma in indian population: a study of 113 cases |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339674/ https://www.ncbi.nlm.nih.gov/pubmed/22557876 http://dx.doi.org/10.4103/0974-620X.94766 |
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