Multicentric Castleman's disease associated with inherited epidermolysis bullosa

Yoshio Kawakami, Akiko Nishibu, Satoshi Kikuchi, Mikio Ohtsuka, Koichiro Nakamura, Yoshihiro Nozawa, Masafumi Abe, Keiji Iwatsuki, Fumio Kaneko

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


Multicentric Castleman's disease (MCD) is a rare disorder characterized by fever, polyclonal hypergammaglobulinemia, and generalized lymphadenopathy. It has three histological characteristics: a recognizable architecture, germinal center abnormalities, and plasmacytosis. Inherited epidermolysis bullosa (EB) is also a rare disorder caused by a genetic defect. We report a 43-year-old patient with dystrophic EB, non-Hallopeau-Siemens recessive type or dominant type, displaying clinicopathologic features of MCD. In addition, his serum interleukin-6, which is thought to be responsible for the clinical symptoms in MCD, was elevated.

Original languageEnglish
Pages (from-to)689-693
Number of pages5
JournalJournal of Dermatology
Issue number9
Publication statusPublished - Sept 1 2003
Externally publishedYes


  • Dystrophic epidermolysis bullosa
  • Hypergammaglobulinemia
  • Interleukin-6

ASJC Scopus subject areas

  • Dermatology


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