Korean J Med.
1999 Jan;56(1):98-102.
A Case of Reflex Sympathetic Dystrophy Syndrome developed after Protein Losing Enteropathy
- Affiliations
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- 1Department of Internal Medicine Inha University College of Medicine, Inchon, Korea.
- 2Department of Nuclear Medicine Inha University College of Medicine, Inchon, Korea.
Abstract
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A 16-year old girl was admitted for chronic diarrhea, generalized edema, severe pain of lower
extremities, and general weakness. She could not walk because of burning pain of knee and ankle.
99mTc-MDP bone scan demonstrated increased periarticular uptake in both lower extremity with
focal increased activity in proximal portion of both tibias.. Abnormal abdominal activity in
ascending, transverse, and descending colon is also seen. Bone densitometry showed severe
osteoporosis in lower extremity. 99mTc-HSA scan showed abnormal radioactivity in small bowel,
and descending colon indicating protein losing enteropathy. Endoscopic biopsy of terminal ileum
showed a few dilated lymphatics in the submucosa. After steroid and supplemental therapy,
the symptoms and signs of both protein losing enteropathy and RSDS much improved simultaneously.
Reflex sympathetic dystrophy syndrome is a complex of symptoms characterized by severe pain,
swelling, autonomic vasomotor dysfunction, and impaired mobility of affected extremities.
The important causes are trauma, fracture, and inflammation. We assumed that the reflex
sympathetic dystrophy syndrome of this girl was due to protein losing enteropathy. And as far
as we know there has not been reported case that protein losing enteropathy assumed as a cause
of reflex sympathetic dystrophy syndrome.