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Autoreactive Antibodies Associated with Castleman Disease Triad

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Publisher Wiley
Date 2024 Mar 14
PMID 38482465
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Abstract

The Castleman triad has been described in a select few patients presenting with a retroperitoneal mass, mucocutaneous pemphigus vulgaris, and bronchiolitis obliterans. Here, we describe the Castleman triad in a 19-year-old male with unicentric hyaline vascular type Castleman disease (HV-CD). This patient presented with an array of positive antibodies, including anti-cyclic citrullinated peptide, anti-double-stranded DNA, and Sjogren's IgG. Interestingly, the patient's rheumatologic symptoms resolved after tumor resection, while his antibody profile remained relatively unchanged. HV-CD, with a triad presentation, was thought to be from a paraneoplastic syndrome secondary to an underlying lymphoproliferative disorder. The findings presented here identify multiple autoantibodies potentially contributing to this patient's presentation with HV-CD.

Citing Articles

Case Report: A rare pediatric case of paraneoplastic pemphigus associated with Castleman disease misdiagnosed as Behçets disease.

Zhang R, Liu J, Nie N, Wang D, Wu J, Zhang H Front Pediatr. 2024; 12:1469495.

PMID: 39649406 PMC: 11620853. DOI: 10.3389/fped.2024.1469495.

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