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Chronic Myelomonocytic Leukemia following Multicentric Castleman Disease

Multicentric Castleman disease (MCD) is a rare nonmalignant lymphoproliferative disorder presenting systemic symptoms such as fever, night sweats, fatigue, anemia, effusions, and multifocal lymphadenopathy. The etiology of MCD has not been clarified to date. The coexistence of MCD with chronic myelo...

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Detalles Bibliográficos
Autores principales: Li, Feng, Zhang, Xiaomei, Guo, Yanting, Zhu, Yuandong, Wu, Yicun, Ling, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828649/
https://www.ncbi.nlm.nih.gov/pubmed/29607228
http://dx.doi.org/10.1155/2018/5895903
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author Li, Feng
Zhang, Xiaomei
Guo, Yanting
Zhu, Yuandong
Wu, Yicun
Ling, Yun
author_facet Li, Feng
Zhang, Xiaomei
Guo, Yanting
Zhu, Yuandong
Wu, Yicun
Ling, Yun
author_sort Li, Feng
collection PubMed
description Multicentric Castleman disease (MCD) is a rare nonmalignant lymphoproliferative disorder presenting systemic symptoms such as fever, night sweats, fatigue, anemia, effusions, and multifocal lymphadenopathy. The etiology of MCD has not been clarified to date. The coexistence of MCD with chronic myelomonocytic leukemia (CMML) has been rarely reported. Although the pathogenesis remains unclear, this association probably reflects an incidental and fortuitous finding rather than the alteration of a common pluripotent stem cell precursor. Herein, we report on one case of MCD coexisting with CMML and elucidate the underlying mechanism of pathology in some aspects.
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spelling pubmed-58286492018-04-01 Chronic Myelomonocytic Leukemia following Multicentric Castleman Disease Li, Feng Zhang, Xiaomei Guo, Yanting Zhu, Yuandong Wu, Yicun Ling, Yun Case Rep Hematol Case Report Multicentric Castleman disease (MCD) is a rare nonmalignant lymphoproliferative disorder presenting systemic symptoms such as fever, night sweats, fatigue, anemia, effusions, and multifocal lymphadenopathy. The etiology of MCD has not been clarified to date. The coexistence of MCD with chronic myelomonocytic leukemia (CMML) has been rarely reported. Although the pathogenesis remains unclear, this association probably reflects an incidental and fortuitous finding rather than the alteration of a common pluripotent stem cell precursor. Herein, we report on one case of MCD coexisting with CMML and elucidate the underlying mechanism of pathology in some aspects. Hindawi 2018-01-23 /pmc/articles/PMC5828649/ /pubmed/29607228 http://dx.doi.org/10.1155/2018/5895903 Text en Copyright © 2018 Feng Li et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Li, Feng
Zhang, Xiaomei
Guo, Yanting
Zhu, Yuandong
Wu, Yicun
Ling, Yun
Chronic Myelomonocytic Leukemia following Multicentric Castleman Disease
title Chronic Myelomonocytic Leukemia following Multicentric Castleman Disease
title_full Chronic Myelomonocytic Leukemia following Multicentric Castleman Disease
title_fullStr Chronic Myelomonocytic Leukemia following Multicentric Castleman Disease
title_full_unstemmed Chronic Myelomonocytic Leukemia following Multicentric Castleman Disease
title_short Chronic Myelomonocytic Leukemia following Multicentric Castleman Disease
title_sort chronic myelomonocytic leukemia following multicentric castleman disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828649/
https://www.ncbi.nlm.nih.gov/pubmed/29607228
http://dx.doi.org/10.1155/2018/5895903
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