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Subcutaneous amyloid-tumor of beta-2-microglobulin origin in a long-term hemodialysis patient.

作者信息

Floege J, Brandis A, Nonnast-Daniel B, Westhoff-Bleck M, Tiedow G, Linke R P, Koch K M

机构信息

Department of Nephrology, Medizinische Hochschule, Hannover, FRG.

出版信息

Nephron. 1989;53(1):73-5. doi: 10.1159/000185706.

DOI:10.1159/000185706
PMID:2674745
Abstract

beta 2-Microglobulin (beta 2M)-derived amyloidosis has become a major concern in long-term hemodialysis patients. Clinical symptomatology is largely restricted to the articular and periarticular sites and in rare cases systemic manifestations have been described. We present a long-term hemodialysis patient, who after 16 years of hemodialysis with regenerated cellulosic membranes not only had a bilateral carpal tunnel syndrome, cystic bone translucencies and humeroscapular periarthritis but also developed two subcutaneous tumors in both gluteal regions, causing discomfort when sitting. Histology, immunohistology and electron microscopy of the tumor from the right side showed that it consisted of beta 2M-derived amyloid with concurrent scattered amyloid infiltration of the overlying skin. This report therefore adds a new clinical manifestation to the symptomatology of this type of amyloid.

摘要

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Pseudotumoral amyloidosis of beta 2-microglobulin origin in the buttock of a patient receiving long term haemodialysis.
一名长期接受血液透析患者臀部的β2-微球蛋白源性假瘤样淀粉样变。
J Clin Pathol. 1993 Aug;46(8):771-2. doi: 10.1136/jcp.46.8.771.
4
Generalized amyloidosis from beta 2-microglobulin, with caecal perforation after long-term haemodialysis.β2微球蛋白所致的全身性淀粉样变,长期血液透析后出现盲肠穿孔。
Virchows Arch A Pathol Anat Histopathol. 1991;419(4):349-53. doi: 10.1007/BF01606526.