A case report of Degos disease in patient presented with jejunal perforation and peritonitis

ผู้แต่ง

  • Sujirod Hanthavichai DIVISION OF DERMATOLOGY, DEPARMENT OF MEDICINE, FACULTY OF MEDICINE, CHULALONGKORN UNIVERSITY, BANGKOK, THAILAND
  • Ratchathorn Panchaprateep DIVISION OF DERMATOLOGY, DEPARMENT OF MEDICINE, FACULTY OF MEDICINE, CHULALONGKORN UNIVERSITY, BANGKOK, THAILAND
  • Noppadon Noppakun DIVISION OF DERMATOLOGY, DEPARMENT OF MEDICINE, FACULTY OF MEDICINE, CHULALONGKORN UNIVERSITY, BANGKOK, THAILAND

คำสำคัญ:

Degos disease, intestinal perforation

บทคัดย่อ

Degos disease or malignant atrophic papulosis is a progressive small- and medium-size arterial occluding disease, leading to tissue infarction in many organs such as the skin, gastrointestinal and nervous systems. This study reported a 56-year-old female patient who presented with abdominal pain due to jejunal perforation with peritonitis. Later, she developed generalized multiple central white scar and telangiectatic rim on trunk, extremities, palm and sole. The histopathology is characteristic, with wedge-shaped area of homogenized collagen fibers and lymphocytic vasculitis in the dermis. Unfortunately, she died from sepsis and multiorgan failure.

เอกสารอ้างอิง

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ดาวน์โหลด

เผยแพร่แล้ว

2026-06-11

รูปแบบการอ้างอิง

Hanthavichai, S., Panchaprateep, R., & Noppakun, N. (2026). A case report of Degos disease in patient presented with jejunal perforation and peritonitis. วารสารโรคผิวหนัง, 27(3), 198–203. สืบค้น จาก https://he02.tci-thaijo.org/index.php/TJD/article/view/282955

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