SummaryWe report an unusual case of cardiac sarcoidosis demonstrated by interventricular septal thickening. A 64-year-old woman was diagnosed with sarcoidosis involving the lungs, eyes, and skin. Three years later, renal dysfunction was detected during a periodic examination and a renal biopsy revealed non-caseating granulomas. Electrocardiogram results were normal, but an echocardiogram revealed thickening of the interventricular septum. Abnormal accumulation of gallium-67 and a perfusion defect in tecnetium-99-methoxyisobutylisonitrile scintigrams occurred in the interventricular septum. Magnetic resonance images showed T2-high intensity in the lesion. We considered the thickening to represent cardiac involvement of sarcoidosis. Oral prednisolone therapy diminished the interventricular septal thickening. (Int Heart J 2014; 55: 181-183) Key words: Interventricular septum S arcoidosis is a multisystem infl ammatory disease of unknown etiology. Interventricular thinning is the most specifi c characteristic feature of cardiac sarcoidosis in echocardiograms, 1) whereas interventricular septal thickening is extremely rare in sarcoidosis patients.2,3) Here, we report an unusual case of cardiac sarcoidosis that presented as interventricular septal thickening.
Case ReportIn May 2008, a 64-year-old woman developed eye fl oaters and erythema on the forehead. A chest X-ray fi lm and computed tomography scans revealed enlargement of the bilateral hilar and mediastinal lymph nodes and nodular shadows in the lung fi elds. She was admitted to our hospital for further examination. Her serum angiotensin converting enzyme (ACE) levels were normal (21.2 IU/L, baseline 8.3-21.4 IU/L), but her serum lysozyme levels were elevated (19.0 μg/mL, baseline 5.0-10.2 μg/mL). A gallium-67 scintigram revealed abnormal uptake in the mediastinal and bilateral hilar lymph nodes. An electrocardiogram, 24-hour Holter electrocardiogram, echocardiogram, and tecnetium-99-methoxyisobutylisonitrile scintigram revealed no abnormal fi ndings. A transbronchial lung biopsy and a skin biopsy showed non-caseating granulomas. She was definitively diagnosed with sarcoidosis involving the lungs, eyes, and skin. Routine periodic examination with an electrocardiogram and echocardiogram revealed no abnormality. Her serum creatinine, ACE, and lysozyme levels gradually increased after January 2011, and renal involvement of the sarcoidosis was suspected. In June 2011, she was admitted to our hospital again for further examination. Fine crackles were heard over both lung fi elds. Systolic murmurs were heard at the third intercostal space just left of the sternum. Laboratory data revealed elevated serum levels of ACE (26.5 IU/L, baseline 8.3-21.4 IU/L), lysozyme (27.4 μg/mL, baseline 5.0-10.2 μg/mL), and creatinine (1.95 mg/dL, 0.40 -1.10 mg/dL). Histopathologic examination of kidney biopsy specimens revealed non-caseating epithelioid granulomas with giant cells, compatible with sarcoidosis. Electrocardiogram and 24-hour Holter electrocardiogram findings were norm...