Title
Brachial plexitis: an unusual presentation in sickle cell disease
Document Type
Article
Publication Title
Journal of Community Hospital Internal Medicine Perspectives
Abstract
Brachial plexitis is defined as an inflammation of the brachial plexus. There are two entities of the disease: idiopathic, which is generally considered to be immune-mediated, and genetic. The disease manifests as the acute onset shoulder pain, weakness of the involving arm ± sensory loss. Brachial plexitis is also known as Parsonage-Turner syndrome and hereditary neuralgic amyotrophy. Diagnosis is made with the help of history, physical exam, and imaging. Conservative management is the mainstay of treatment. There has not been any proven treatment for the condition though some cases have been treated empirically with steroids. We present a case of 61-year-old woman with sickle cell anemia who presented with right upper extremity weakness and MRI findings of brachial plexitis.
First Page
437
Last Page
439
DOI
https://doi.org/10.1080/20009666.2019.1659665
Publication Date
Fall 11-1-2019
Recommended Citation
Dawood M, McArthur J, Tauseef A. Brachial plexitis: an unusual presentation in sickle cell disease. J Community Hosp Intern Med Perspect. 2019 Nov 1;9(5):437-439. doi: 10.1080/20009666.2019.1659665. PMID: 31723392; PMCID: PMC6830239.