J Korean Acad Rehabil Med.  2000 Dec;24(6):1229-1234.

Inclusion Body Myositis: A case report

Affiliations
  • 1Department of Rehabilitation Medicine, Bong Seng Hospital.
  • 2Department of Rehabilitation Medicine, Sung Ae Hospital.

Abstract

In 1971 inclusion body myositis was reported by Yunis and Samaha. This disease is similar with chronic multiple myositis clinically. Pathologically, inclusion body myositis is characterized by intracytoplasmic vacuole with degenerating fibers and accompanied with inclusion body in internal nucleus and cytoplasm. Since then 240 cases of inclusion body myositis have been reported in the world including 3 cases in Korea. A 27 years-old lady had inclusion body myositis, which show slowly progressive muscular weakness. We confirmed this with clinical symptom, muscle biopsy, and electrophysiologic study. We report the typical manifestation of inclusion body myositis in a 27 years-old lady with the brief review of literature.

Keyword

Inclusion body myositis; Vacuole; Progressive muscular weakness; Muscle biopsy; Electrophysiological study

MeSH Terms

Adult
Biopsy
Cytoplasm
Humans
Inclusion Bodies*
Korea
Muscle Weakness
Myositis, Inclusion Body*
Polymyositis
Vacuoles
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