Minkowitz G, Smoller B R, McNutt N S
Department of Pathology and Medicine, New York Hospital-Cornell University Medical Center, New York.
Arch Dermatol. 1991 Oct;127(10):1520-3.
Benign cutaneous polyarteritis nodosa has been described as having a benign course in contrast to that of systemic classic polyarteritis nodosa. We tested the hypothesis that this histologic distinction is false by reviewing nine consecutive cases with the histologic diagnosis of benign cutaneous polyarteritis nodosa. Our study revealed that on follow-up, seven (78%) of nine cases had evidence of involvement of at least one organ other than the skin, with the kidney being the organ most commonly involved. Four (44%) of nine patients had serologic evidence of hepatitis B infection, one had cryoglobulinemia, and one had polyclonal hypergammaglobulinemia associated with acquired immunodeficiency syndrome. We conclude that benign cutaneous polyarteritis nodosa is not necessarily benign and is closely related to systemic polyarteritis nodosa.
与系统性典型结节性多动脉炎相比,良性皮肤结节性多动脉炎被描述为具有良性病程。我们通过回顾连续9例经组织学诊断为良性皮肤结节性多动脉炎的病例,检验了这种组织学差异是错误的这一假设。我们的研究显示,随访发现,9例中有7例(78%)有证据表明至少有一个非皮肤器官受累,其中肾脏是最常受累的器官。9例患者中有4例(44%)有乙型肝炎感染的血清学证据,1例有冷球蛋白血症,1例有与获得性免疫缺陷综合征相关的多克隆高球蛋白血症。我们得出结论,良性皮肤结节性多动脉炎不一定是良性的,且与系统性结节性多动脉炎密切相关。