Atypical Presentation of Amyloidosis in a Female Patient with Muscle Weakness.
Journal
Case reports in medicine
ISSN: 1687-9627
Titre abrégé: Case Rep Med
Pays: United States
ID NLM: 101512910
Informations de publication
Date de publication:
2023
2023
Historique:
received:
04
08
2022
revised:
26
02
2023
accepted:
17
03
2023
medline:
24
4
2023
pubmed:
24
4
2023
entrez:
24
04
2023
Statut:
epublish
Résumé
Muscle involvement represents a well-recognized but rare manifestation of amyloidosis. Here, we report a 40-year-old female who presented with muscle weakness, musculoskeletal pain, and proteinuria, which was eventually diagnosed as myopathic amyloidosis based on muscle biopsy results. A multidisciplinary approach appears to be the cornerstone of the diagnostic work up for recognizing the unusual amyloid myopathy.
Identifiants
pubmed: 37090743
doi: 10.1155/2023/1553163
pmc: PMC10118899
doi:
Types de publication
Case Reports
Langues
eng
Pagination
1553163Informations de copyright
Copyright © 2023 Raziyeh Lashkari et al.
Déclaration de conflit d'intérêts
The authors declare that they have no conflicts of interest.
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