Literature DB >> 11588639

Amyloidotic muscle pseudohypertrophy: case report.

R H Scola1, L C Werneck, C S Ramos, R Pasquini, H Graf, W O Arruda.   

Abstract

The authors report one case of amyloidosis associated with muscular pseudohypertrophy in a 46-year-old woman, who developed weakness, macroglossia and muscle hypertrophy associated with primary systemic amyloidosis. Electromyography showed a myopathic pattern and bilateral carpal tunnel syndrome. The muscle biopsy presented with a type I and II fiber hypertrophy and infiltration of amyloid material in the interstitious space and artery walls. She underwent bone marrow transplantation with stabilization and subjective improvement of the clinical picture.

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Year:  2001        PMID: 11588639     DOI: 10.1590/s0004-282x2001000400018

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  2 in total

1.  Chronic myopathy due to immunoglobulin light chain amyloidosis.

Authors:  Irini Manoli; Justin Y Kwan; Qian Wang; Elisabeth J Rushing; Maria Tsokos; Andrew E Arai; Warner M Burch; Angela Dispenzieri; Alexandra C McPherron; William A Gahl
Journal:  Mol Genet Metab       Date:  2013-02-04       Impact factor: 4.797

2.  Muscle involvement with pseudohypertrophy in systemic light chain amyloidosis: Case report.

Authors:  Mirela Draghici; Andreea Jercan; Sorina Nicoleta Badelita; Ruxandra Maria Irimia; Alexandra Eugenia Bastian; Camelia Dobrea; Monica Popescu; Daniel Coriu
Journal:  Medicine (Baltimore)       Date:  2021-12-23       Impact factor: 1.817

  2 in total

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