Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/29678
Title: Isolated rhabdomyolysis of long head of triceps mimicking upper extremity deep vein thrombosis.
Austin Authors: Filipopoulos, Benjamin;Balanathan, Sharmila
Affiliation: Medicine, Northern Hospital Epping, Epping, Victoria, Australia..
Vascular Surgery, Epworth HealthCare, Richmond, Victoria, Australia..
Surgery
Issue Date: 30-Mar-2022
Date: 2022
Publication information: BMJ case reports 2022; 15(3): e245478
Abstract: Rhabdomyolysis is characterised by skeletal muscle breakdown, with release of toxic intracellular contents into the circulation. A man in his 20s presented to the emergency department with acute-onset right arm swelling, with pitting oedema extending into his forearm without clear precipitant. Initial differential diagnosis was upper extremity deep vein thrombosis, however none was identified on CT venogram. Instead, rhabdomyolysis of long head of triceps was diagnosed after multidisciplinary review of the venogram by the treating vascular surgeon and radiologist. Retrospectively, added serum creatine kinase was found to be 11 587 U/L, and together with MRI of the right arm, the diagnosis was established. Given the patient's lack of comorbidities, normal renal function and reliability, he was managed conservatively as an outpatient without hospital admission for intravenous hydration. This is the only case to our knowledge of isolated long head of triceps' rhabdomyolysis reported in Australia and the second case worldwide.
URI: https://ahro.austin.org.au/austinjspui/handle/1/29678
DOI: 10.1136/bcr-2021-245478
Journal: BMJ case reports
PubMed URL: 35354574
PubMed URL: https://pubmed.ncbi.nlm.nih.gov/35354574/
Type: Journal Article
Subjects: muscle disease
musculoskeletal and joint disorders
musculoskeletal syndromes
vascular surgery
Appears in Collections:Journal articles

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