Cutaneous mantle cell lymphoma: A rare case report
Cutaneous mantle cell lymphoma (MCL) is a very rare entity with very few cases reported till date. We report a case of 69-year-old man with generalized lymphadenopathy who was diagnosed with mitotically active B-cell lymphoma and a year later developed multiple large maculopapular skin rashes which...
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Wolters Kluwer Medknow Publications
2020-01-01
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doaj-51e7c97b139e4bdebb79b03783f049b92021-08-09T09:52:01ZengWolters Kluwer Medknow PublicationsClinical Dermatology Review2542-551X2542-55282020-01-0141616310.4103/CDR.CDR_58_18Cutaneous mantle cell lymphoma: A rare case reportSalwa BanoVeena RamaswamyB N TejaswiniChaitra ChandrashekarCutaneous mantle cell lymphoma (MCL) is a very rare entity with very few cases reported till date. We report a case of 69-year-old man with generalized lymphadenopathy who was diagnosed with mitotically active B-cell lymphoma and a year later developed multiple large maculopapular skin rashes which on biopsy showed infiltration of large atypical blast-like cells in the skin and on immunohistochemistry was in favor of MCL-blastoid variant. Skin involvement is rare in MCL, although in some cases, cutaneous manifestations are the first symptom. Skin involvement suggests a disseminated disease and is often associated with blastoid cytological features. Awareness of skin manifestations of MCL is crucial for dermatologists and hematologists for prompt diagnosis and timely treatment. Moreover, it has a dismal prognosis and shows a poor response to standard treatment.http://www.cdriadvlkn.org/article.asp?issn=2542-551X;year=2020;volume=4;issue=1;spage=61;epage=63;aulast=Banocutaneous lymphomacyclin d1mantle cell lymphoma |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Salwa Bano Veena Ramaswamy B N Tejaswini Chaitra Chandrashekar |
spellingShingle |
Salwa Bano Veena Ramaswamy B N Tejaswini Chaitra Chandrashekar Cutaneous mantle cell lymphoma: A rare case report Clinical Dermatology Review cutaneous lymphoma cyclin d1 mantle cell lymphoma |
author_facet |
Salwa Bano Veena Ramaswamy B N Tejaswini Chaitra Chandrashekar |
author_sort |
Salwa Bano |
title |
Cutaneous mantle cell lymphoma: A rare case report |
title_short |
Cutaneous mantle cell lymphoma: A rare case report |
title_full |
Cutaneous mantle cell lymphoma: A rare case report |
title_fullStr |
Cutaneous mantle cell lymphoma: A rare case report |
title_full_unstemmed |
Cutaneous mantle cell lymphoma: A rare case report |
title_sort |
cutaneous mantle cell lymphoma: a rare case report |
publisher |
Wolters Kluwer Medknow Publications |
series |
Clinical Dermatology Review |
issn |
2542-551X 2542-5528 |
publishDate |
2020-01-01 |
description |
Cutaneous mantle cell lymphoma (MCL) is a very rare entity with very few cases reported till date. We report a case of 69-year-old man with generalized lymphadenopathy who was diagnosed with mitotically active B-cell lymphoma and a year later developed multiple large maculopapular skin rashes which on biopsy showed infiltration of large atypical blast-like cells in the skin and on immunohistochemistry was in favor of MCL-blastoid variant. Skin involvement is rare in MCL, although in some cases, cutaneous manifestations are the first symptom. Skin involvement suggests a disseminated disease and is often associated with blastoid cytological features. Awareness of skin manifestations of MCL is crucial for dermatologists and hematologists for prompt diagnosis and timely treatment. Moreover, it has a dismal prognosis and shows a poor response to standard treatment. |
topic |
cutaneous lymphoma cyclin d1 mantle cell lymphoma |
url |
http://www.cdriadvlkn.org/article.asp?issn=2542-551X;year=2020;volume=4;issue=1;spage=61;epage=63;aulast=Bano |
work_keys_str_mv |
AT salwabano cutaneousmantlecelllymphomaararecasereport AT veenaramaswamy cutaneousmantlecelllymphomaararecasereport AT bntejaswini cutaneousmantlecelllymphomaararecasereport AT chaitrachandrashekar cutaneousmantlecelllymphomaararecasereport |
_version_ |
1721214613627863040 |