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Sarcoidosis, granulomas and myopathy syndromes: A clinical-pathology review
被引:6
|作者:
Garret, Mark
[1
]
Pestronk, Alan
[1
,2
,3
]
机构:
[1] Washington Univ, Dept Neurol, Sch Med, St Louis, MO 63110 USA
[2] Washington Univ, Pathol & Immunol, Sch Med, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Neurol, 660 South Euclid Ave, Box 8111, St Louis, MO 63110 USA
关键词:
Myopathy;
Sarcoidosis;
Granuloma;
Myositis;
INCLUSION-BODY MYOSITIS;
MUSCLE INVOLVEMENT;
MUSCULOSKELETAL SARCOIDOSIS;
IMAGING FINDINGS;
FEATURES;
D O I:
10.1016/j.jneuroim.2022.577975
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Muscle involvement in sarcoidosis is common by pathologic analysis, but symptomatic disorders are less frequent. Sarcoidosis-related muscle pathology includes non-caseating granulomas, muscle fiber changes that are diffuse or anatomically related to granulomas, and perimysial connective tissue with histiocyte-associated damage. The mechanisms by which granulomas form, enlarge and damage muscle tissues are incompletely understood. Sarcoidosis-related clinical syndromes with muscle involvement include: chronic myopathies with proximal weakness; nodular disorders; subacute onset disorders involving proximal or eye muscles; myalgia or fatigue syndromes; and, possibly, inclusion body myositis-like disorders. Corticosteroid treatment may benefit some syndromes, but clinical trials are necessary.
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页数:9
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