MeSH 搜索器

Malignant Atrophic Papulosis

Variously described as a vasculopathy, endovasculitis, or occlusive arteriopathy, this condition occurs in a benign cutaneous form and a lethal multiorgan systemic variant. It is characterized by a narrowing and occlusion of the lumen of small to medium-sized blood vessels, leading to ischemia and infarction in the involved organ systems. The etiology and pathophysiology are unknown.
推出的年份: 2008
副标题
树号: C14.907.137.520, C14.907.940.530, C17.800.862.457
MeSH 单一 ID: D054853
进入的组:
  • Atrophic Papuloses, Malignant
  • Atrophic Papulosis, Malignant
  • Malignant Atrophic Papuloses
  • Papuloses, Malignant Atrophic
  • Degos Syndrome
  • Syndrome, Degos
  • Degos's Malignant Atrophic Papulosis
  • Kohlmeier-Degos Disease
  • Disease, Kohlmeier-Degos
  • Papulosis, Malignant Atrophic
  • Degos Disease
  • Disease, Degos
  • Erythrokeratoderma en cocardes

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