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Diagnosis and Symptomatic Treatment of Early Reactive Cardiac Amyloidosis in Systemic Sclerosis
Journal of Rheumatic Diseases ; : 132-136, 2015.
Article in English | WPRIM | ID: wpr-202429
ABSTRACT
Systemic sclerosis as a connective tissue disease could affect all internal organs of the body and could also manifest as a cutaneous lesion. Cardiac involvement leading to cardiac manifestations in systemic sclerosis patients is not rare. However, cardiac amyloidosis combined with systemic sclerosis is extremely rare. Although there were no definite treatment options in this case, symptomatic treatment is the cornerstone of the management plan. In this case report, we described a correct diagnosis and symptomatic medical care of early reactive cardiac amyloidosis with systemic sclerosis and summarize the current state of the relevant literature.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Scleroderma, Systemic / Cardiomyopathy, Restrictive / Connective Tissue Diseases / Diagnosis / Amyloidosis Type of study: Diagnostic study Limits: Humans Language: English Journal: Journal of Rheumatic Diseases Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Scleroderma, Systemic / Cardiomyopathy, Restrictive / Connective Tissue Diseases / Diagnosis / Amyloidosis Type of study: Diagnostic study Limits: Humans Language: English Journal: Journal of Rheumatic Diseases Year: 2015 Type: Article