A Case of Familial Cardiac Amyloidosis
Korean Circulation Journal
;
: 520-526, 2004.
Artículo
en Coreano
| WPRIM
| ID: wpr-133528
ABSTRACT
Amyloidosis is defined by the extracellular deposition of fibrillar proteinacious material that binds Congo red dye. Amyloid fibrils can be deposited locally, but can involve virtually every organ system of the body. Hereditary, autosomal dominant amyloidosis, caused by mutations in the genes encoding transthyretin, fibrinogen Aalpha-chain, lysozyme or apolipoprotein A-I, is-extremely rare. A case of familial amyloidosis, involving the heart, was identified, where the patient complained exertional dyspnea. The echocardiographic findings were the markedly thickened the interventricular septum and right ventricular wall, as well as a granular sparkling appearance in the interventricular septum. On admission, the patient, and his younger brother, underwent endomyocardial biopsies, and the results of the Congo red staining and EM were consistent with amyloidosis. The patient was managed conservatively, and discharged without complication.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Biopsia
/
Fibrinógeno
/
Prealbúmina
/
Ecocardiografía
/
Muramidasa
/
Apolipoproteína A-I
/
Rojo Congo
/
Amiloidosis Familiar
/
Hermanos
/
Disnea
Tipo de estudio:
Estudio pronóstico
Límite:
Humanos
Idioma:
Coreano
Revista:
Korean Circulation Journal
Año:
2004
Tipo del documento:
Artículo
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