| Literature DB >> 18751957 |
Duck-Woo Kim1, Sung-Bum Kang, Kyung Ho Lee, Ghee-Young Choe, So Yeon Park, Mikhaylyuk Nicholay.
Abstract
Degos' disease, otherwise known as "malignant atrophic papulosis," is a rare condition characterized by typical cutaneous lesions. Its involvement of the gastrointestinal (GI) tract is usually associated with a poor prognosis. We report a case of Degos' disease with GI involvement, which ultimately caused peritonitis, sepsis, and death, despite all treatment measures. A 59-year old woman was admitted to our hospital with acute generalized abdominal pain. The patient had presented initially with multiple skin lesions 2 years earlier, and even with surgery for small-bowel perforation 10 months before this admission, Degos' disease had not been diagnosed. Explorative laparotomy revealed multifocal, ischemic changes in the small bowel with perforation in the mid-jejunum. After the operation, she suffered recurrent small-bowel fistulas and died within 3 months. In a patient with acute abdominal pain and typical atrophic papules, clinicians should retain a high index of suspicion for Degos' disease with GI involvement, even though it is rare.Entities:
Mesh:
Year: 2008 PMID: 18751957 DOI: 10.1007/s00595-007-3728-9
Source DB: PubMed Journal: Surg Today ISSN: 0941-1291 Impact factor: 2.549