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Cardiac sarcoidosis preceded by sick sinus syndrome presenting as biventricular involvement and intracardiac giant thrombus: a case report.
Hirai, Akeo; Shiraishi, Yasuyuki; Fukuda, Keiichi; Fujita, Jun.
Afiliación
  • Hirai A; Department of Cardiology, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo 160-8582, Japan.
  • Shiraishi Y; Department of Cardiology, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo 160-8582, Japan.
  • Fukuda K; Department of Cardiology, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo 160-8582, Japan.
  • Fujita J; Department of Cardiology, Keio University School of Medicine, 35 Shinanomachi Shinjuku-ku, Tokyo 160-8582, Japan.
Eur Heart J Case Rep ; 7(9): ytad435, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37705943
ABSTRACT

Background:

Sarcoidosis is a granulomatous disorder characterized by the formation of non-necrotizing granulomas in various organs. Cardiac sarcoidosis presents with various clinical, anatomical, and electrophysiological manifestations. As cardiac involvement is related to adverse outcomes, the early diagnosis of cardiac sarcoidosis is crucial and sometimes challenging. Case

summary:

A 65-year-old woman was initially treated for sick sinus syndrome (SSS) with normal cardiac function. Cardiac conduction defects and biventricular dysfunction continued to progress over a short clinical course, and the patient was eventually referred to our hospital for further investigation and treatment of cardiogenic shock due to pacemaker pacing failure. An echocardiography revealed a large thrombus formation in the right ventricle and atrium. An urgent thrombectomy was performed, and myocardial biopsy confirmed the diagnosis of cardiac sarcoidosis. Steroid pulse therapy was initiated and was effective in treating the cardiogenic shock. One year after discharge, the patient manifested with sustained ventricular tachycardia and ultimately died of severe cardiac pump failure. On autopsy, diffuse fibrotic tissues were noted in both ventricles and atria.

Discussion:

While conduction abnormalities, such as right bundle brunch block and atrioventricular block, are common clinical manifestations, SSS is rarely reported as a primary manifestation of cardiac sarcoidosis. Thus, clinicians should ensure that sufficient investigations are carried out when diagnosing idiopathic SSS.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Screening_studies Idioma: En Revista: Eur Heart J Case Rep Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Screening_studies Idioma: En Revista: Eur Heart J Case Rep Año: 2023 Tipo del documento: Article País de afiliación: Japón