Synchronous brain and intravascular B‐cell lymphoma after remission of an adult hemophagocytic syndrome

Hemophagocytic lymphohistiocytosis (HLH) should be considered in the differential diagnosis of adult patients with white matter disease. Brain involvement can be life‐threatening and should prompt aggressive therapy. Even after HLH remission, the possibility of subsequent deterioration due to emerge...

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Autores principales: Fonseca, Válter R., Espada, Eduardo, Geraldes, Ruth, Ortiz, Santiago, Sousa, Rita, Lopez, Dolores, Silva, Marisa Teixeira, Victorino, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831375/
https://www.ncbi.nlm.nih.gov/pubmed/27099719
http://dx.doi.org/10.1002/ccr3.507
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author Fonseca, Válter R.
Espada, Eduardo
Geraldes, Ruth
Ortiz, Santiago
Sousa, Rita
Lopez, Dolores
Silva, Marisa Teixeira
Victorino, Rui
author_facet Fonseca, Válter R.
Espada, Eduardo
Geraldes, Ruth
Ortiz, Santiago
Sousa, Rita
Lopez, Dolores
Silva, Marisa Teixeira
Victorino, Rui
author_sort Fonseca, Válter R.
collection PubMed
description Hemophagocytic lymphohistiocytosis (HLH) should be considered in the differential diagnosis of adult patients with white matter disease. Brain involvement can be life‐threatening and should prompt aggressive therapy. Even after HLH remission, the possibility of subsequent deterioration due to emergence of an aggressive intravascular lymphoma is highlighted here.
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spelling pubmed-48313752016-04-20 Synchronous brain and intravascular B‐cell lymphoma after remission of an adult hemophagocytic syndrome Fonseca, Válter R. Espada, Eduardo Geraldes, Ruth Ortiz, Santiago Sousa, Rita Lopez, Dolores Silva, Marisa Teixeira Victorino, Rui Clin Case Rep Case Reports Hemophagocytic lymphohistiocytosis (HLH) should be considered in the differential diagnosis of adult patients with white matter disease. Brain involvement can be life‐threatening and should prompt aggressive therapy. Even after HLH remission, the possibility of subsequent deterioration due to emergence of an aggressive intravascular lymphoma is highlighted here. John Wiley and Sons Inc. 2016-02-16 /pmc/articles/PMC4831375/ /pubmed/27099719 http://dx.doi.org/10.1002/ccr3.507 Text en © 2016 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Fonseca, Válter R.
Espada, Eduardo
Geraldes, Ruth
Ortiz, Santiago
Sousa, Rita
Lopez, Dolores
Silva, Marisa Teixeira
Victorino, Rui
Synchronous brain and intravascular B‐cell lymphoma after remission of an adult hemophagocytic syndrome
title Synchronous brain and intravascular B‐cell lymphoma after remission of an adult hemophagocytic syndrome
title_full Synchronous brain and intravascular B‐cell lymphoma after remission of an adult hemophagocytic syndrome
title_fullStr Synchronous brain and intravascular B‐cell lymphoma after remission of an adult hemophagocytic syndrome
title_full_unstemmed Synchronous brain and intravascular B‐cell lymphoma after remission of an adult hemophagocytic syndrome
title_short Synchronous brain and intravascular B‐cell lymphoma after remission of an adult hemophagocytic syndrome
title_sort synchronous brain and intravascular b‐cell lymphoma after remission of an adult hemophagocytic syndrome
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831375/
https://www.ncbi.nlm.nih.gov/pubmed/27099719
http://dx.doi.org/10.1002/ccr3.507
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