Amyloid myopathy presenting with respiratory failure.
Author(s) -
John R. Ashe,
Cecil O. Borel,
G Hart,
Richard L. Humphrey,
D A Derrick,
Ralph W. Kuncl
Publication year - 1992
Publication title -
journal of neurology neurosurgery and psychiatry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.391
H-Index - 206
eISSN - 1468-330X
pISSN - 0022-3050
DOI - 10.1136/jnnp.55.2.162
Subject(s) - macroglossia , myopathy , medicine , pathology , respiratory failure , amyloidosis , pathological , diaphragm (acoustics) , infiltration (hvac) , muscle biopsy , weakness , amyloid (mycology) , respiratory system , biopsy , anatomy , tongue , physics , acoustics , loudspeaker , thermodynamics
Amyloidosis is a rare cause of myopathy. Its prominent or presenting feature may be respiratory failure. Physiological measurement of transdiaphragmatic pressure and biopsy specimens of muscle show the pathological mechanism to be diaphragm weakness due to amyloid infiltration of the diaphragm rather than parenchymal lung involvement. Thus amyloid myopathy even without the typical macroglossia and muscle pseudohypertrophy should be considered as one of the neurological causes of respiratory failure.
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