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Isolated Tuberculous Myositis: A Systematic Review and Multicenter Cases
Ji Hyoun Kim1, Jeong Seok Lee2, Byoong Yong Choi3
1Division of Rheumatology, Department of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
Isolated tuberculous myositis (ITBM) presents uniquely and has severe outcomes, particularly in immunocompromised individuals. Dermatomyositis/polymyositis is a common underlying condition in these rare extrapulmonary tuberculosis cases.
Area of Science:
- Infectious Diseases
- Rheumatology
- Pulmonology
Background:
- Isolated tuberculous myositis (ITBM) is a rare form of extrapulmonary tuberculosis.
- Understanding its clinical features and associated conditions is crucial for diagnosis and management.
Purpose of the Study:
- To investigate the clinical features and underlying conditions of isolated tuberculous myositis (ITBM).
- To analyze the outcomes of ITBM, especially in immunocompromised patients.
Main Methods:
- A systematic literature search and a multicenter survey were conducted.
- Data from identified ITBM cases were extracted and analyzed for underlying conditions, presentations, treatments, and outcomes.
Main Results:
- 58 ITBM cases (9 pediatric) were identified. Immunocompromised patients had shorter symptom duration and higher multilocular involvement.
- Dermatomyositis/polymyositis (DM/PM) was a common underlying disease in immunocompromised adults with ITBM.
- ITBM had a grave outcome, especially in immunocompromised hosts, with higher mortality in survey-identified cases.
Conclusions:
- ITBM presents uniquely with fever, tenderness, swelling, erythema, and abscess formation.
- DM/PM is a highly prevalent underlying disease in immunocompromised ITBM patients.
- ITBM poses a significant risk, particularly for immunocompromised individuals.
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