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原发性皮肤淀粉样变:25例临床、实验室及组织病理学研究。通过免疫荧光法鉴定病变中的γ球蛋白和C3。

Primary cutaneous amyloidosis: clinical, laboratorial and histopathological study of 25 cases. Identification of gammaglobulins and C3 in the lesions by immunofluorescence.

作者信息

Habermann M C, Montenegro M R

出版信息

Dermatologica. 1980;160(4):240-8. doi: 10.1159/000250500.

Abstract

25 cases of primary cutaneous amyloidosis are studied. 16 patients had macular amyloidosis (MPA) and 9 lichen amyloidosus (LPA). gamma-Globulins were increased in 50% of the patients. IgG and IgA were increased in the serum of 5 and 3 patients with MPA and 4 and 2 patients with LPA, respectively. Volume of amyloid deposits was similar in both forms. By direct immunofluorescence we demonstrated IgG in the amyloid deposits of 21 of the 25 cases and C3 in 13; IgM was present in 9 cases of MPA and in 3 cases of LPA. MPA was more frequent than LPA; histologically, it was impossible to distinguish MPA from LPA; correlation between serum levels of gamma-globulins and their presence in amyloid deposits was weak; MPA and LPA seem to be distinct clinical manifestations of the same disease and itching does not cause transformation of MPA in LPA.

摘要

对25例原发性皮肤淀粉样变进行了研究。16例患者为斑状淀粉样变(MPA),9例为苔藓样淀粉样变(LPA)。50%的患者γ球蛋白升高。MPA患者中有5例、LPA患者中有4例血清IgG升高;MPA患者中有3例、LPA患者中有2例血清IgA升高。两种类型中淀粉样沉积物的量相似。通过直接免疫荧光法,我们在25例中的21例淀粉样沉积物中检测到IgG,13例中检测到C3;9例MPA和3例LPA中存在IgM。MPA比LPA更常见;在组织学上,无法将MPA与LPA区分开来;血清γ球蛋白水平与其在淀粉样沉积物中的存在之间的相关性较弱;MPA和LPA似乎是同一疾病的不同临床表现,瘙痒不会导致MPA转变为LPA。

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