| Literature DB >> 19730402 |
Nariaki Toita1, Nobuaki Kawamura, Norikazu Hatano, Syun-ichiro Takezaki, Yuka Ohkura, Masafumi Yamada, Motohiko Okano, Tadao Okada, Fumiaki Sasaki, Kanako C Kubota, Tomoo Itoh, Tadashi Ariga.
Abstract
Castleman disease (CD) is a rare lymphoproliferative disorder of unknown etiology. It is quite difficult to diagnose CD without typical localized signs or symptoms. We present a 5-year-old boy with unicentric plasma cell CD in the mesentery, which was too small to be detected by any conventional imaging. (18)F-fluorodeoxyglucose positron emission tomography image and a serum cytokine profile prompted us to perform a curative surgical excision, confirming his diagnosis. Our case also supported an important role of interleukin-6 in the pathophysiology of plasma cell CD.Entities:
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Year: 2009 PMID: 19730402 DOI: 10.1097/MPH.0b013e3181b2708f
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289