| Literature DB >> 31282978 |
Hyo Jung Kim1, Ju Hee Han, Chul Hwan Bang, Kyung Shin Park, Seok-Goo Cho, Dong Su Yoo, Kyung Moon Kim, Hyun Jung Park, Young Min Park, Jun Young Lee, Ji Hyun Lee.
Abstract
Castleman's disease is a rare disease of the lymph nodes and related tissues, presenting as angiofollicular or giant lymph node hyperplasia. Although various skin manifestations have been reported to occur in Castleman's disease, a comprehensive study of cutaneous disorders in Castleman's disease is lacking. Therefore, the aim of this study was to investigate Castleman's disease-associated cutaneous disorders. The medical records of 57 patients with Castleman's disease who visited our hospitals from January 2007 to May 2018 were analysed retrospectively. Patients were classified according to the presence of skin involvement. Plasma variant-type Castleman's disease and multicentric Castleman's disease were more commonly found in patients with Castleman's disease with a cutaneous disorder than in those without a cutaneous disorder. In addition, the skin disorders were classified according to pathomechanisms: immune complex-related (paraneoplastic pemphigus, xanthogranulomas), cytokine-related (vasculitis-like lesion, cherry angioma, hyperpigmentation), and non-specific (pruritus). This study builds on previous case reports of cutaneous disorders in Castleman's disease and proposes a new classification system.Entities:
Keywords: POEMS syndrome; interleukin-6; lymphoproliferative disorder; paraneoplastic itch; Castleman’s disease
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Year: 2019 PMID: 31282978 DOI: 10.2340/00015555-3253
Source DB: PubMed Journal: Acta Derm Venereol ISSN: 0001-5555 Impact factor: 4.437