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Diaphragmatic Castleman's disease: A rare lymphoproliferative disorder: Clinical and radiological perspectives
Journal article   Peer reviewed

Diaphragmatic Castleman's disease: A rare lymphoproliferative disorder: Clinical and radiological perspectives

Pritish Aher, Raed Zughul, Sameer Samtani, Sarv Priya, Yoel Siegel and Chris Schettino
Radiology case reports, Vol.19(12), pp.6390-6393
12/2024
DOI: 10.1016/j.radcr.2024.09.077
PMCID: PMC11461952
PMID: 39387026

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Abstract

Castleman's disease (CD) is a rare, benign nonclonal lymphoproliferative disorder with an unclear etiology, presenting significant diagnostic challenges due to its nonspecific features. CD is categorized into unicentric (UCD) and multicentric (MCD) types, with MCD further divided into HHV-8-associated and idiopathic (iMCD) forms. Clinical manifestations include fever, weight loss, night sweats, and organomegaly, with specific symptoms depending on the subtype. Diagnostic criteria for CD involve a combination of major criteria-histopathologic examination and minor criteria. Imaging techniques, including CT, MRI, and PET-CT, play a crucial role in diagnosis, staging, and differentiation from other diseases. This paper discusses the pathophysiology, clinical features, diagnostic criteria, and imaging findings of CD, illustrated by a case of a patient with renal disease with incidentally detected a right cardiophrenic mass. The case highlights the importance of comprehensive imaging and clinical evaluation in managing CD.
Cardiophrenic mass Diaphragmatic mass Lymphoproliferative disorders Thoracic Castleman disease Thoracic liposarcoma

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