Literature DB >> 843255

Amyloidosis with plasma cell dyscrasia. An overlooked caused of adult onset sensorimotor neuropathy.

J L Trotter, W K Engel, F I Ignaczak.   

Abstract

In ten previously undiagnosed patients, we have found erstwhile-"primary" nonhereditary amyloidosis as an overlooked cause of a predominately sensory, painful, and hyperesthetic distal neuropathy occurring in middle-age and older patients. These symptoms, associated with orthostatic hypotension, diarrhea or constipation, cardiac abnormality, and male impotence are virtually diagnostic (in the absence of diabetes mellitus). Tissue diagnosis is quickly made by crystal-violet metachromasia of amyloid in fresh-frozen sections of a muscle biopsy specimen. Immunoglobulin and bone marrow evidence of plasma cell dyscrasia in eight of the ten patients suggests that the neuropathy in this form of amyloidosis is actually secondary to a plasma-cell-originating dysproteinemia. Therapy with melphalan and prednisone was not of benefit.

Entities:  

Mesh:

Year:  1977        PMID: 843255     DOI: 10.1001/archneur.1977.00500160023003

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  10 in total

1.  Clinical Autonomic Research Society Proceedings. Abstracts.

Authors: 
Journal:  Clin Auton Res       Date:  1992-02       Impact factor: 4.435

2.  Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy.

Authors:  G Boysen; G Galassi; Z Kamieniecka; J Schlaeger; W Trojaborg
Journal:  J Neurol Neurosurg Psychiatry       Date:  1979-11       Impact factor: 10.154

3.  AL amyloidosis mimicking a preferentially autonomic chronic Guillain-Barré syndrome.

Authors:  T Lingenfelser; R P Linke; S Dette; W Roggendorf; H Wiethölter
Journal:  Clin Investig       Date:  1992-02

4.  Characterization of amyloid deposits in biopsies of 15 with "sporadic" (non-familial or plasma cell dyscrasia amyloid polyneuropathy.

Authors:  M C Dalakas; G Cunningham
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

5.  Ultrastructural immunolabelling of amyloid fibrils in acquired and hereditary amyloid neuropathies.

Authors:  D Adams; G Said
Journal:  J Neurol       Date:  1996-01       Impact factor: 4.849

6.  Neuropathy, amyloidosis, and monoclonal gammopathy.

Authors:  J W Fitting; A Bischoff; F Regli; G De Crousaz
Journal:  J Neurol Neurosurg Psychiatry       Date:  1979-03       Impact factor: 10.154

7.  Neuropathy in IgM lambda paraproteinemia. Immunoreactivity to neural proteins and chondroitin sulfate.

Authors:  W C Yee; A F Hahn; S A Hearn; A R Rupar
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

8.  Nature of amyloid deposits in hypernephroma. Immunocytochemical studies in 2 cases associated with amyloid polyneuropathy.

Authors:  M C Dalakas; S Fujihara; V Askanas; W K Engel; G G Glenner
Journal:  Am J Pathol       Date:  1984-09       Impact factor: 4.307

9.  Myopathy in primary systemic amyloidosis.

Authors:  M A Gertz; R A Kyle
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-06       Impact factor: 10.154

10.  Clinical Neuropathology practice guide 3-2014: combined nerve and muscle biopsy in the diagnostic workup of neuropathy - the Bordeaux experience.

Authors:  Anne Vital; Claude Vital
Journal:  Clin Neuropathol       Date:  2014 May-Jun       Impact factor: 1.368

  10 in total

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