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Clinical and Pathological Analysis of Two Cases of Cutaneous Malignant Melanoma

ABSTRACT: The purpose of this study was the clinical and histo-immunohistochemical analysis of two cases: a cutaneous pigmented facial malignant melanoma and a lumbar congenital nevus with malignant transformation. A series of clinical elements raised the suspicion of some malignant melanocytic lesi...

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Autores principales: BLENDEA, A., GEORGESCU, D.M., PURCARU, Ş.O., TACHE, D.E., FLOREA, I, STOICA, L.E., ȚOLEA, I, GEORGESCU, C.V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medical University Publishing House Craiova 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246982/
https://www.ncbi.nlm.nih.gov/pubmed/30534430
http://dx.doi.org/10.12865/CHSJ.41.03.14
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author BLENDEA, A.
GEORGESCU, D.M.
PURCARU, Ş.O.
TACHE, D.E.
FLOREA, I
STOICA, L.E.
ȚOLEA, I
GEORGESCU, C.V.
author_facet BLENDEA, A.
GEORGESCU, D.M.
PURCARU, Ş.O.
TACHE, D.E.
FLOREA, I
STOICA, L.E.
ȚOLEA, I
GEORGESCU, C.V.
author_sort BLENDEA, A.
collection PubMed
description ABSTRACT: The purpose of this study was the clinical and histo-immunohistochemical analysis of two cases: a cutaneous pigmented facial malignant melanoma and a lumbar congenital nevus with malignant transformation. A series of clinical elements raised the suspicion of some malignant melanocytic lesions and the histopathological analysis through the paraffin embedding technique confirmed the clinical suspicion. The immunohistochemical analysis using the streptavidin-biotin-peroxydase method of the facial malignant melanoma showed: S100 protein intense and diffuse positive, Tyrosinase diffuse positive, HMB45 strong and focal positive, Cyclin D1 positive in approximately 40% and Ki-67 positive in almost 70% of the tumor cells. The malignant melanoma developed on the nevocellular nevus displayed: S100 protein intense and diffuse positive, both in the nevus cells and in the malignant melanocytes as well, Tyrosinase intense and diffuse positive in the malignant melanocytes, poor and focal positive in the nevus cells and HMB45 intense and focal positive in the malignant cells and positive in the isolated nevus cells. Cyclin D1 was positive in about 70% of the malignant cells, but negative in the nevus area and Ki-67 was found positive in relatively 30% of the malignant melanocytes, also in less than 1% of the nevus cells. The pattern and the intensity of the Tyrosinase and HMB45 immunoexpression are important in the differentiation of the nevus cells from the malignant melanocytic cells. The immunoexpression of Cyclin D1 does not correlate directly with the proliferating activity of the malignant melanocytic cells in all types of malignant melanomas.
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spelling pubmed-62469822018-12-10 Clinical and Pathological Analysis of Two Cases of Cutaneous Malignant Melanoma BLENDEA, A. GEORGESCU, D.M. PURCARU, Ş.O. TACHE, D.E. FLOREA, I STOICA, L.E. ȚOLEA, I GEORGESCU, C.V. Curr Health Sci J Case Report ABSTRACT: The purpose of this study was the clinical and histo-immunohistochemical analysis of two cases: a cutaneous pigmented facial malignant melanoma and a lumbar congenital nevus with malignant transformation. A series of clinical elements raised the suspicion of some malignant melanocytic lesions and the histopathological analysis through the paraffin embedding technique confirmed the clinical suspicion. The immunohistochemical analysis using the streptavidin-biotin-peroxydase method of the facial malignant melanoma showed: S100 protein intense and diffuse positive, Tyrosinase diffuse positive, HMB45 strong and focal positive, Cyclin D1 positive in approximately 40% and Ki-67 positive in almost 70% of the tumor cells. The malignant melanoma developed on the nevocellular nevus displayed: S100 protein intense and diffuse positive, both in the nevus cells and in the malignant melanocytes as well, Tyrosinase intense and diffuse positive in the malignant melanocytes, poor and focal positive in the nevus cells and HMB45 intense and focal positive in the malignant cells and positive in the isolated nevus cells. Cyclin D1 was positive in about 70% of the malignant cells, but negative in the nevus area and Ki-67 was found positive in relatively 30% of the malignant melanocytes, also in less than 1% of the nevus cells. The pattern and the intensity of the Tyrosinase and HMB45 immunoexpression are important in the differentiation of the nevus cells from the malignant melanocytic cells. The immunoexpression of Cyclin D1 does not correlate directly with the proliferating activity of the malignant melanocytic cells in all types of malignant melanomas. Medical University Publishing House Craiova 2015 2015-03-15 /pmc/articles/PMC6246982/ /pubmed/30534430 http://dx.doi.org/10.12865/CHSJ.41.03.14 Text en Copyright © 2015, Medical University Publishing House Craiova http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited.
spellingShingle Case Report
BLENDEA, A.
GEORGESCU, D.M.
PURCARU, Ş.O.
TACHE, D.E.
FLOREA, I
STOICA, L.E.
ȚOLEA, I
GEORGESCU, C.V.
Clinical and Pathological Analysis of Two Cases of Cutaneous Malignant Melanoma
title Clinical and Pathological Analysis of Two Cases of Cutaneous Malignant Melanoma
title_full Clinical and Pathological Analysis of Two Cases of Cutaneous Malignant Melanoma
title_fullStr Clinical and Pathological Analysis of Two Cases of Cutaneous Malignant Melanoma
title_full_unstemmed Clinical and Pathological Analysis of Two Cases of Cutaneous Malignant Melanoma
title_short Clinical and Pathological Analysis of Two Cases of Cutaneous Malignant Melanoma
title_sort clinical and pathological analysis of two cases of cutaneous malignant melanoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246982/
https://www.ncbi.nlm.nih.gov/pubmed/30534430
http://dx.doi.org/10.12865/CHSJ.41.03.14
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