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闭塞性非血管炎性血管病

Occlusive Nonvasculitic Vasculopathy.

作者信息

Llamas-Velasco Mar, Alegría Victoria, Santos-Briz Ángel, Cerroni Lorenzo, Kutzner Heinz, Requena Luis

机构信息

*Associate Staff of the Department of Dermatology, Department of Dermatology, Hospital Universitario de la Princesa, Universidad Autónoma, Madrid, Spain; †Associate Staff of the Department of Dermatology, Department of Dermatology, Fundación Jiménez Diaz, Universidad Autónoma, Madrid, Spain; ‡Director of Dermatopathology, Department of Dermatology, Hospital Clínico Universitario, Salamanca, Spain; §Director of Dermatopathology, Dermatopathology Research Unit, Medical University of Graz, Graz, Austria; ¶Director of Dermatopathology, Dermatopathologie Laboratory, Friedrichschafen, Germany; and ‖Chairman of the Department of Dermatology, Department of Dermatology, Hospital Clínico Universitario, Salamanca, Spain.

出版信息

Am J Dermatopathol. 2017 Sep;39(9):637-662. doi: 10.1097/DAD.0000000000000766.

Abstract

We review the most characteristic clinical and histopathologic findings of the cutaneous manifestations of the occlusive nonvasculitic vasculopathic disorders. Clinically, most of these conditions are characterized by retiform purpura. Histopathologic findings consist of occlusion of the vessel lumina with no vasculitis. Different disorders may produce nonvasculitic occlusive vasculopathy in cutaneous blood and lymphatic vessels, including embolization due to cholesterol and oxalate emboli, cutaneous intravascular metastasis from visceral malignancies, atrial myxomas, intravascular angiosarcoma, intralymphatic histiocytosis, intravascular lymphomas, endocarditis, crystal globulin vasculopathy, hypereosinophilic syndrome, and foreign material. Other times, the occlusive disorder is due to platelet pugging, including heparin necrosis, thrombocytosis secondary to myeloproliferative disorders, paroxysmal nocturnal hemoglobinuria, and thrombotic thrombocytopenic purpura. Occlusive vasculopathy may also appear in cold-related gelling agglutination, like that occurring in cryofibrinogenemia, cryoglobulinemia, cold agglutinin syndrome, and crystalglobulinemia. Microorganisms may also occlude the vessels lumina and this is especially frequent in ecthyma gangrenosum, opportunistic fungi as aspergillosis or fusariosis, Lucio phenomenon of lepromatous leprosy and disseminated strongyloidiasis. Systemic coagulopathies due to defects of C and S proteins, coumarin/warfarin-induced skin necrosis, disseminated intravascular coagulation, and antiphospholipid antibody/lupus anticoagulant syndrome may also result in occlusive nonvasculitic vasculopathy. Finally, vascular coagulopathies such as Sneddon syndrome, livedoid vasculopathy, and atrophic papulosis may also cause occlusion of the vessels of the dermis and/or subcutis. Histopathologic study of occlusive vasculopathic lesions is the first step to achieve an accurate diagnosis, and they should be correlated with clinical history, physical examination, and laboratory findings to reach a final diagnosis.

摘要

我们回顾了闭塞性非血管炎性血管病变的皮肤表现中最具特征性的临床和组织病理学发现。临床上,这些病症大多以网状紫癜为特征。组织病理学发现包括血管腔闭塞且无血管炎。不同的病症可在皮肤血管和淋巴管中产生非血管炎性闭塞性血管病变,包括胆固醇和草酸盐栓子导致的栓塞、内脏恶性肿瘤的皮肤血管内转移、心房黏液瘤、血管内血管肉瘤、淋巴管内组织细胞增多症、血管内淋巴瘤、心内膜炎、晶体球蛋白血管病变、高嗜酸性粒细胞综合征以及异物。其他情况下,闭塞性病症是由于血小板聚集,包括肝素坏死、骨髓增殖性疾病继发的血小板增多症、阵发性夜间血红蛋白尿以及血栓性血小板减少性紫癜。闭塞性血管病变也可能出现在与寒冷相关的凝胶凝集中,如在冷纤维蛋白原血症、冷球蛋白血症、冷凝集素综合征和晶体球蛋白血症中发生的情况。微生物也可能阻塞血管腔,这在坏疽性脓皮病、曲霉菌病或镰刀菌病等机会性真菌、瘤型麻风的卢西奥现象以及播散性类圆线虫病中尤为常见。由于C蛋白和S蛋白缺陷、香豆素/华法林诱导的皮肤坏死、弥散性血管内凝血以及抗磷脂抗体/狼疮抗凝物综合征导致的全身性凝血障碍也可能导致闭塞性非血管炎性血管病变。最后,诸如斯内登综合征、萎缩性丘疹性血管病等血管性凝血障碍也可能导致真皮和/或皮下组织血管闭塞。对闭塞性血管病变损害进行组织病理学研究是实现准确诊断的第一步,并且应将其与临床病史、体格检查和实验室检查结果相关联以达成最终诊断。

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