| Literature DB >> 17616028 |
Jun Bean Park1, Jin Hyeok Hwang, Haeryoung Kim, Hyung Sim Choe, Yu Kyeong Kim, Hong Bin Kim, Soo-Mee Bang.
Abstract
Castleman disease (CD) is a rare lymphoproliferative disorder of unknown etiology with different clinical manifestations. A previous healthy 50 year-old man was hospitalized for right upper quadrant (RUQ) abdominal pain. He had jaundice and a 1 cm-sized lymph node in the right supraclavicular area. Pancreas and biliary computed tomography (CT) showed masses at the right renal hilum and peripancreatic areas. Positron emission tomography (PET) showed widespread systemic lymphadenopathy. Excisional biopsy of the right supraclavicular node revealed a hyaline vascular variant of CD. Corticosteroid therapy was started and the extent of disease decreased. We here report a case of multicentric CD, the hyaline vascular variant, presenting with jaundice, diagnosed by excisional biopsy and successfully treated with corticosteroids.Entities:
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Year: 2007 PMID: 17616028 PMCID: PMC2687612 DOI: 10.3904/kjim.2007.22.2.113
Source DB: PubMed Journal: Korean J Intern Med ISSN: 1226-3303 Impact factor: 2.884