Incomplete POEMS syndrome with multicentric Castleman's disease and amyloidosis

Authors

  • P. González de la Aleja
  • M. García-Navarro
  • R. Sánchez-Martínez
  • J. M. Ramos

DOI:

https://doi.org/10.23938/ASSN.0041

Keywords:

POEMS syndrome. Castleman's disease. Amyloidosis.

Abstract

Castleman's disease (CD) is an atypical lymphoproliferative disorder of unknown cause, characterized by non-clonal nodal hyperplastic growth. Two forms of clinical presentation are currently recognized, one localized and the other multicentric, and four histopathologic variants. It is characterized by generalized lymphadenopathy, hepatosplenomegaly, fever and night sweats.

CD may present severe pancytopenia, multi-organ failure, lymphoma evolution and it can sometimes be associated with paraneoplastic syndromes such as POEMS syndrome. Associations of these two entities have been widely described in the current literature, although its less common association with amyloidosis is described as isolated clinical cases. We report a case with this triple association: EC, POEMS and amyloidosis.

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Author Biographies

P. González de la Aleja

Servcio de Medicina Interna del Hospital General Universitario de Alicante (HGUA).

M. García-Navarro

Servicio de Medicina Interna. Hospital General Universitario de Alicante (HGUA).

R. Sánchez-Martínez

Servicio de Medicina Interna. Hospital General Universitario de Alicante (HGUA)

J. M. Ramos

Servicio de Medicina Interna. Hospital General Universitario de Alicante (HGUA)

References

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Published

2017-12-29

How to Cite

1.
González de la Aleja P, García-Navarro M, Sánchez-Martínez R, Ramos JM. Incomplete POEMS syndrome with multicentric Castleman’s disease and amyloidosis. An Sist Sanit Navar [Internet]. 2017 Dec. 29 [cited 2026 Jan. 23];40(3):475-8. Available from: https://recyt.fecyt.es/index.php/ASSN/article/view/52410

Issue

Section

Clinical notes

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