Corticosteroid myopathy is a severe side effect of corticosteroid application. Although the risk usually increases with drug dosage, even a single dose can lead to substantial muscular damage. Usually the tissue recovers over time after discontinuation of the responsible drug. We report local corticosteroid myopathy in a patient who had been given corticosteroid injections because of chronic hip pain. In this case, the patient's myopathy in the left hip region had not improved after 6 months.

Download full-text PDF

Source
http://dx.doi.org/10.1097/01376517-200610000-00002DOI Listing

Publication Analysis

Top Keywords

corticosteroid myopathy
12
isolated corticosteroid
4
myopathy
4
myopathy gluteal
4
gluteal muscles
4
corticosteroid
4
muscles corticosteroid
4
myopathy severe
4
severe side
4
side corticosteroid
4

Similar Publications

Background: Clinically amyopathic dermatomyositis (CADM) is a rare subtype of idiopathic inflammatory myositis often linked with the presence of autoantibodies targeting melanoma differentiation-associated protein 5 (MDA5). Patients with CADM are at increased risk of developing rapidly progressing interstitial lung disease, which significantly increases both morbidity and mortality compared to other forms of inflammatory myopathies. While there is no standardized treatment regimen, current therapeutic strategies are generally focused on combination immunosuppressive therapies.

View Article and Find Full Text PDF

Focal myositis is a rare, localized, benign, self-limiting, and non-suppurative inflammatory lesion of the skeletal muscle that may occasionally occur as a complication of rheumatic diseases. This case report discusses a 58-year-old patient with rheumatoid arthritis, who was diagnosed with focal myositis during standard immunosuppressive therapy. The patient was treated with tofacitinib; to our knowledge, this is the first reported case of focal myositis managed with this medication.

View Article and Find Full Text PDF

Rheumatic Manifestations of Sarcoidosis.

Diagnostics (Basel)

December 2024

North Bristol NHS Foundation Trust, Bristol BS10 5NB, UK.

Sarcoidosis is a multisystem granulomatous inflammatory disorder, of unknown aetiology, which causes a wide spectrum of clinical phenotypes. It can present at any age, most commonly between 20 and 60 years, with a roughly equal sex distribution. Diagnosis is often delayed due to multiple diagnostic mimics, particularly joint disease.

View Article and Find Full Text PDF

[Clinical characteristics and prognostic analysis of concurrent pneumonia in patients with idiopathic inflammatory myopathy].

Zhonghua Jie He He Hu Xi Za Zhi

January 2025

Department of Pulmonary and Critical Care Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing100730, China.

To describe the clinical characteristics and to explore the prognostic factors of concurrent pneumonia (PJP) in patients with idiopathic inflammatory myopathy (IIM). We retrospectively enrolled consecutive IIM patients diagnosed with PJP at our center between January 2014 and December 2022. Fifty-eight IIM-PJP patients were enrolled in our study, with the age of 26-79 (56.

View Article and Find Full Text PDF

Introduction: Percutaneous needle fasciotomy (PNF) is a non-invasive treatment option for finger flexion contractures caused by Dupuytren's disease. Variations in PNF techniques include the use of corticosteroid injection. In the presented randomised controlled trial, we compare the efficacy of PNF +/- corticosteroid injection in terms of reducing the recurrence rate.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!