Suppr超能文献

胶原血管病患者栅栏状中性粒细胞和肉芽肿性皮炎的组织病理学谱。

The histopathologic spectrum of palisaded neutrophilic and granulomatous dermatitis in patients with collagen vascular disease.

作者信息

Chu P, Connolly M K, LeBoit P E

机构信息

Department of Dermatology, University of California--San Francisco.

出版信息

Arch Dermatol. 1994 Oct;130(10):1278-83.

PMID:7944509
Abstract

BACKGROUND AND DESIGN

Patients with lupus erythematosus, rheumatoid arthritis, and other diseases in which circulating immune complexes occur can develop a papular eruption on the extremities. Terms including Churg-Strauss granuloma, cutaneous extravascular necrotizing granuloma, rheumatoid papules, superficial ulcerating rheumatoid necrobiosis, and interstitial granulomatous dermatitis with arthritis have been given to this entity. We evaluated the clinical and histopathologic features of six patients with systemic lupus erythematosus, two patients with rheumatoid arthritis, and one patient with an incompletely characterized collagen vascular disease who developed cutaneous papules.

RESULTS

The lesions were located largely on the extremities and were symmetrically distributed in most of the patients. They ranged from a few to many and from skin colored to erythematous, and they had smooth, ulcerated, or umbilicated surfaces. Histopathologic examination showed a spectrum of changes that, we believe, reflect the evolution of lesions, ie, leukocytoclastic vasculitis with dense neutrophilic infiltrates and degenerated collagen in early lesions; palisaded granulomas surrounding leukocytoclastic debris, fibrin, and altered collagen in fully developed lesions; and, as the process wanes, palisaded granulomas with dermal fibrosis and scant neutrophilic debris. Each stage of development elicits a different differential diagnosis, which can be resolved by the application of histopathologic criteria.

CONCLUSION

The histopathologic findings are consonant with the evolution of an immune complex-mediated disease. The diverse histopathologic, and sometimes clinical, appearances account for the variety of names given to this condition. We propose the name palisaded neutrophilic and granulomatous dermatitis of immune complex disease to reflect the histopathologic evolution and clinical aspects of this condition.

摘要

背景与设计

红斑狼疮、类风湿关节炎及其他会出现循环免疫复合物的疾病患者,四肢可出现丘疹样皮疹。这一病症曾被赋予多种名称,包括变应性肉芽肿性血管炎、皮肤血管外坏死性肉芽肿、类风湿丘疹、浅表溃疡性类风湿性渐进性坏死、以及伴有关节炎的间质性肉芽肿性皮炎。我们评估了6例系统性红斑狼疮患者、2例类风湿关节炎患者以及1例胶原血管病特征未完全明确但出现皮肤丘疹的患者的临床及组织病理学特征。

结果

皮损大多位于四肢,多数患者呈对称分布。皮疹数量不等,少则几个,多则众多,颜色从肤色到红斑色,表面光滑、溃疡或呈脐凹状。组织病理学检查显示一系列变化,我们认为这些变化反映了皮损的演变过程,即早期皮损表现为白细胞破碎性血管炎,伴有密集中性粒细胞浸润和变性胶原;完全发展的皮损表现为围绕白细胞破碎性碎片、纤维蛋白和变性胶原的栅栏状肉芽肿;随着病情缓解,出现伴有真皮纤维化和少量中性粒细胞碎片的栅栏状肉芽肿。每个发展阶段都引发不同的鉴别诊断,可通过应用组织病理学标准来解决。

结论

组织病理学发现与免疫复合物介导疾病的演变过程相符。多样的组织病理学表现,有时还有临床外观,导致了这一病症被赋予多种名称。我们提议将其命名为免疫复合物病的栅栏状中性粒细胞和肉芽肿性皮炎,以反映该病症的组织病理学演变及临床特点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验