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Primary cutaneous follicle center lymphoma

Cutaneous lymphomas are classified according to their cellular origin into T-cell lymphoma and B-cell lymphoma. The annual incidence rate is 0.3 per 100,000 population. We report a case of a 56-year-old male patient who presented with a two-month history of nodules of varying sizes, some ulcerated,...

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Autores principales: Costa, Eline Pinheiro Weba, de Lucena, Bethänia Dias, Amin, Gabriela Athayde, Bittencourt, Maraya de Jesus Semblano, Dias Junior, Leonidas Braga, Pires, Carla Andréa Avelar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682700/
https://www.ncbi.nlm.nih.gov/pubmed/29166511
http://dx.doi.org/10.1590/abd1806-4841.20175457
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author Costa, Eline Pinheiro Weba
de Lucena, Bethänia Dias
Amin, Gabriela Athayde
Bittencourt, Maraya de Jesus Semblano
Dias Junior, Leonidas Braga
Pires, Carla Andréa Avelar
author_facet Costa, Eline Pinheiro Weba
de Lucena, Bethänia Dias
Amin, Gabriela Athayde
Bittencourt, Maraya de Jesus Semblano
Dias Junior, Leonidas Braga
Pires, Carla Andréa Avelar
author_sort Costa, Eline Pinheiro Weba
collection PubMed
description Cutaneous lymphomas are classified according to their cellular origin into T-cell lymphoma and B-cell lymphoma. The annual incidence rate is 0.3 per 100,000 population. We report a case of a 56-year-old male patient who presented with a two-month history of nodules of varying sizes, some ulcerated, on the face, abdomen, and upper limbs. Histopathological examination and immunohistochemical study confirmed the diagnosis of primary cutaneous centrofollicular lymphoma. Studies have shown an increased incidence of non-Hodgkin lymphomas in the last decade. We report an infrequent case that should be kept as a differential diagnosis of patients with nodules and cutaneous papules.
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spelling pubmed-56827002017-11-16 Primary cutaneous follicle center lymphoma Costa, Eline Pinheiro Weba de Lucena, Bethänia Dias Amin, Gabriela Athayde Bittencourt, Maraya de Jesus Semblano Dias Junior, Leonidas Braga Pires, Carla Andréa Avelar An Bras Dermatol Case Report Cutaneous lymphomas are classified according to their cellular origin into T-cell lymphoma and B-cell lymphoma. The annual incidence rate is 0.3 per 100,000 population. We report a case of a 56-year-old male patient who presented with a two-month history of nodules of varying sizes, some ulcerated, on the face, abdomen, and upper limbs. Histopathological examination and immunohistochemical study confirmed the diagnosis of primary cutaneous centrofollicular lymphoma. Studies have shown an increased incidence of non-Hodgkin lymphomas in the last decade. We report an infrequent case that should be kept as a differential diagnosis of patients with nodules and cutaneous papules. Sociedade Brasileira de Dermatologia 2017 /pmc/articles/PMC5682700/ /pubmed/29166511 http://dx.doi.org/10.1590/abd1806-4841.20175457 Text en ©2017 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Case Report
Costa, Eline Pinheiro Weba
de Lucena, Bethänia Dias
Amin, Gabriela Athayde
Bittencourt, Maraya de Jesus Semblano
Dias Junior, Leonidas Braga
Pires, Carla Andréa Avelar
Primary cutaneous follicle center lymphoma
title Primary cutaneous follicle center lymphoma
title_full Primary cutaneous follicle center lymphoma
title_fullStr Primary cutaneous follicle center lymphoma
title_full_unstemmed Primary cutaneous follicle center lymphoma
title_short Primary cutaneous follicle center lymphoma
title_sort primary cutaneous follicle center lymphoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682700/
https://www.ncbi.nlm.nih.gov/pubmed/29166511
http://dx.doi.org/10.1590/abd1806-4841.20175457
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