Gran J T
Revmatologisk avdeling Regionsykehuset i Tromsø.
Tidsskr Nor Laegeforen. 1997 Apr 30;117(11):1627-9.
Approximately 1 - 7% of all patients with cutaneous vasculitis have an associated malignant disease. In such cases, vasculitis most often accompanies myelo- and lymphoproliferative diseases. Histologically, leukocytoclastic or panarteritis nodosa-like vasculitis are the most frequently observed types, and in most instances manifest clinically as palpable purpura. Malignancy should be suspected if the clinical picture does not fit into any well defined category of connective tissue disease, and when drugs and infection are excluded as causes of the vasculitis. The author discusses possible mechanisms of paramalignant vasculitis.
所有皮肤血管炎患者中约有1% - 7%伴有恶性疾病。在这种情况下,血管炎最常伴随骨髓和淋巴增殖性疾病。组织学上,白细胞破碎性或结节性多动脉炎样血管炎是最常观察到的类型,在大多数情况下临床上表现为可触及的紫癜。如果临床表现不符合任何明确的结缔组织病类别,且排除药物和感染作为血管炎的病因时,应怀疑有恶性肿瘤。作者讨论了副肿瘤性血管炎的可能机制。