| Literature DB >> 25627230 |
Denise de Fatima Forteski1, Fernanda Calil Machado Netto1, Andrea Barranjard Vannucci Lomonte1, Bruno César Cavalcanti dos Anjos1, Maria Claudia Nogueira Zerbini2, Cristiano Augusto de Freitas Zerbini3.
Abstract
Castleman's disease (CD) is a polyclonal lymphoproliferative disorder also known as giant nodular hyperplasia or angiofollicular lymph node hyperplasia. It is a rare disease often associated to human immunodeficiency virus (HIV) and human herpes virus 8 (HHV-8). Histopathological findings in Castleman's disease suggest an exaggerated response to antigenic stimuli seen in other diseases associated with immune activation, such as rheumatoid arthritis. An important aspect of its pathogenesis is the autonomous production of interleukin-6 (IL-6). In this disease, the clinical manifestations are associated to IL-6 serum levels, and surgical removal of the compromised lymph nodes or use of anti-IL-6 antibodies can slow down the symptoms. We describe a multicentric Castleman's disease in a young woman not associated to HHV-8 virus infection or immunosuppression. A short review of the literature follows the description of this clinical case.Entities:
Keywords: Anaemia; Anemia; Autoimmune; Autoimune; B lymphocytes; Castleman's disease; Doença de Castleman; Inflamação; Inflammation; Interleucina‐6; Interleukyn‐6; Linfócitos B
Mesh:
Year: 2014 PMID: 25627230 DOI: 10.1016/j.rbr.2013.05.004
Source DB: PubMed Journal: Rev Bras Reumatol ISSN: 0482-5004