大疱性淀粉样变。超微结构研究的病例报告。
Bullous amyloidosis. Case report with ultrastructural studies.
作者信息
Bluhm J F, Johnson S C, Norback D H
出版信息
Arch Dermatol. 1980 Oct;116(10):1164-8. doi: 10.1001/archderm.116.10.1164.
PMID:7000009
Abstract
A 51-year-old man with primary systemic amyloidosis initially manifested periorbital purpura; later, skin fragility and hemorrhagic bullae developed. The bullae healed with formation of milia. The bullae were shown by electron microscopy to result from breaks in the fragile dermal amyloid deposits well below the basal lamina.
摘要
一名患有原发性系统性淀粉样变性的51岁男性最初表现为眶周紫癜；随后出现皮肤脆弱和出血性大疱。大疱愈合后形成粟丘疹。电子显微镜显示，大疱是由基底膜下方脆弱的真皮淀粉样沉积物破裂所致。
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