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坏疽性脓皮病的组织病理学和免疫病理学研究。

Histopathologic and immunopathologic study of pyoderma gangrenosum.

作者信息

Su W P, Schroeter A L, Perry H O, Powell F C

出版信息

J Cutan Pathol. 1986 Oct;13(5):323-30. doi: 10.1111/j.1600-0560.1986.tb00466.x.

Abstract

Sixty-three patients with pyoderma gangrenosum were seen and studied at the Mayo Clinic from 1971 to 1980. Biopsies from the erythematous border or necrotic edge of the pyoderma gangrenosum lesions usually demonstrated a characteristic pathogenic morphologic evolution. The early lesions revealed mild to moderate perivascular lymphocytic infiltrate associated with endothelial swelling. The fully developed lesions demonstrated necrosis in addition to a dense lymphocytic infiltration surrounding as well as involving the blood vessels. Extravasation of erythrocytes and thrombosis sometimes were seen. Ulceration, infarction, and abscess formation were found in the later stages of evolution. Direct immunofluorescence results were positive in the blood vessels of 36 of 65 (55%) specimens. IgM, C3, and fibrin were found in the papillary and reticular dermal vessels. IgG and IgA were only occasionally present. Pyoderma gangrenosum appears to be a reactive process that is manifested as a vasculitis. Biopsy material from the advancing active erythematous border has early characteristic dermatopathologic findings of lymphocytic vasculitis. Cutaneous vascular immune deposits suggest an immune pathogenesis of either an immune complex disease or lymphocytotoxic reaction.

摘要

1971年至1980年期间,梅奥诊所共诊治了63例坏疽性脓皮病患者并进行了研究。坏疽性脓皮病病变的红斑边缘或坏死边缘的活检通常显示出特征性的致病形态学演变。早期病变表现为轻度至中度血管周围淋巴细胞浸润伴内皮肿胀。完全发展的病变除了血管周围和血管内有密集的淋巴细胞浸润外,还显示出坏死。有时可见红细胞外渗和血栓形成。在演变后期发现溃疡、梗死和脓肿形成。65份标本中有36份(55%)的血管直接免疫荧光结果呈阳性。在乳头层和网状真皮血管中发现了IgM、C3和纤维蛋白。IgG和IgA仅偶尔出现。坏疽性脓皮病似乎是一种表现为血管炎的反应性过程。来自进行性活动性红斑边缘的活检材料具有淋巴细胞性血管炎的早期特征性皮肤病理表现。皮肤血管免疫沉积物提示免疫复合物疾病或淋巴细胞毒性反应的免疫发病机制。

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