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Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome

Thrombocytopenia, anasarca, myelofibrosis, renal dysfunction and organomegaly (TAFRO) syndrome is a variant of Castleman's disease recently identified in Japan. A 73-year-old man was diagnosed with TAFRO syndrome according to clinical findings, and his symptoms improved after corticosteroid the...

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Autores principales: Ohya, Eiko, Mizutani, Minoru, Sakaguchi, Haruna, Sekine, Takao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088550/
https://www.ncbi.nlm.nih.gov/pubmed/27725549
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author Ohya, Eiko
Mizutani, Minoru
Sakaguchi, Haruna
Sekine, Takao
author_facet Ohya, Eiko
Mizutani, Minoru
Sakaguchi, Haruna
Sekine, Takao
author_sort Ohya, Eiko
collection PubMed
description Thrombocytopenia, anasarca, myelofibrosis, renal dysfunction and organomegaly (TAFRO) syndrome is a variant of Castleman's disease recently identified in Japan. A 73-year-old man was diagnosed with TAFRO syndrome according to clinical findings, and his symptoms improved after corticosteroid therapy. Ten months later, lymphadenopathy worsened during tapering of corticosteroids. Histological findings of abdominal lymph nodes showed diffuse large B-cell lymphoma. After 6 cycles of R-CHOP therapy, he has remained in sustained complete remission. This is a rare case of the development of malignant lymphoma during the treatment of TAFRO syndrome, which suggests an association between diffuse large B-cell lymphoma and TAFRO syndrome.
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spelling pubmed-50885502016-11-07 Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome Ohya, Eiko Mizutani, Minoru Sakaguchi, Haruna Sekine, Takao Intern Med Case Report Thrombocytopenia, anasarca, myelofibrosis, renal dysfunction and organomegaly (TAFRO) syndrome is a variant of Castleman's disease recently identified in Japan. A 73-year-old man was diagnosed with TAFRO syndrome according to clinical findings, and his symptoms improved after corticosteroid therapy. Ten months later, lymphadenopathy worsened during tapering of corticosteroids. Histological findings of abdominal lymph nodes showed diffuse large B-cell lymphoma. After 6 cycles of R-CHOP therapy, he has remained in sustained complete remission. This is a rare case of the development of malignant lymphoma during the treatment of TAFRO syndrome, which suggests an association between diffuse large B-cell lymphoma and TAFRO syndrome. The Japanese Society of Internal Medicine 2016-10-01 /pmc/articles/PMC5088550/ /pubmed/27725549 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Ohya, Eiko
Mizutani, Minoru
Sakaguchi, Haruna
Sekine, Takao
Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome
title Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome
title_full Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome
title_fullStr Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome
title_full_unstemmed Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome
title_short Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome
title_sort diffuse large b-cell lymphoma during corticosteroid therapy for tafro syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088550/
https://www.ncbi.nlm.nih.gov/pubmed/27725549
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