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Mitochondrial respiratory function in multiple symmetrical lipomatosis: report of two cases.

  • T. P. Wu*
  • , J. G. Tsai
  • , P. H. Chan
  • , H. C. Lee
  • , Y. H. Wei
  • *Corresponding author for this work
  • Cardinal Tien Hospital, Taiwan

Research output: Contribution to journalJournal Article peer-review

12 Scopus citations

Abstract

Madelung's disease is a rare benign disorder characterized by symmetrical deposition of adipose tissue on the neck and shoulders. The cause of Madelung's disease is obscure and may be associated with mitochondrial dysfunction. In this communication, we report two cases encountered at Cardinal Tien Hospital during 1992. Besides physical check-up and laboratory examination, adipose tissue and muscle biopsies from the biceps brachii were performed. As lipid metabolism is closely related to mitochondrial respiration, biochemical studies may be of great value in clarifying the pathogenetic mechanism of Madelung's disease. We thus determined the activities of mitochondrial respiratory enzymes (NADH cytochrome c reductase, succinate cytochrome c reductase, cytochrome c oxidase) in muscle and blood cells and revealed that the electron transport functions were all elevated. Molecular analysis of mitochondrial DNA from the muscle and blood cells of both patients failed to find large-scale deletion or point mutations.

Original languageEnglish
Pages (from-to)513-518
Number of pages6
JournalJournal of the Formosan Medical Association
Volume93
Issue number6
StatePublished - 06 1994
Externally publishedYes

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