Literature DB >> 17665027

POEMS (polyneuropathy, organomegaly, endocrinopathy, M protein, skin lesions) syndrome: a South America's report.

Ana Claudia Celestino Leite1, Osvaldo J M Nascimento, Marco Antonio Lima, Maria José Andrada-Serpa.   

Abstract

The POEMS syndrome, also known as Crow-Fukase syndrome, is an unusual systemic disorder described mainly in Asian individuals. It is characterized by the presence of (P)polyneuropathy, (O)organomegaly, (E)endocrinopathy, (M) M-protein, and (S) skin changes. Several other associated conditions such as sclerotic bone lesions, Castleman disease, low-grade fever, edema and hematologic disorders are usually seen. We describe five Brazilian patients with this syndrome. Two patients presented Castleman disease, one patient presented osteosclerotic myeloma and in two patients no associated conditions were found.

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Year:  2007        PMID: 17665027     DOI: 10.1590/s0004-282x2007000300030

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  2 in total

1.  Adenopathy and Extensive Skin Patch Overlying a Plasmacytoma (AESOP) Syndrome.

Authors:  Uzma Farooq; Sonal Choudhary; Michael P McLeod; Daniele Torchia; Franco Rongioletti; Paolo Romanelli
Journal:  J Clin Aesthet Dermatol       Date:  2012-11

2.  Mitral valve prolapse and the association with cutaneous mucin infiltration: ("cardiocutaneous mucinosis").

Authors:  Uzma Farooq; Sonal Choudhary; Michael P McLeod; Daniele Torchia; Paolo Romanelli
Journal:  J Clin Aesthet Dermatol       Date:  2013-05
  2 in total

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