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½ÉÀåÀ̽ÄÀ¸·Î Ä¡·áµÈ ½ÉÀ¯À°Á¾Áõ - 1¿¹ º¸°í - Cardiac Sarcoidosis Treated by Cardiac Transplantation - A Case Report -

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ÀåÀçÁ¤ ( Jang Jae-Jung ) 
¿ï»ê´ëÇб³ ÀÇ°ú´ëÇÐ ¼­¿ïÁß¾Óº´¿ø Áø´Üº´¸®Çб³½Ç

¹Î±¤¼± ( Min Kwang-Seon ) 
¿ï»ê´ëÇб³ ÀÇ°ú´ëÇÐ ¼­¿ïÁß¾Óº´¿ø Áø´Üº´¸®Çб³½Ç
Á¤°æõ ( Jung Gyeong-Cheon ) 
¿ï»ê´ëÇб³ ÀÇ°ú´ëÇÐ ¼­¿ïÁß¾Óº´¿ø Áø´Üº´¸®Çб³½Ç
±èÀçÁß ( Kim Jae-Joong ) 
¿ï»ê´ëÇб³ ÀÇ°ú´ëÇÐ ¼­¿ïÁß¾Óº´¿ø ³»°ú
ÀÌÀÎö ( Lee In-Chul ) 
¿ï»ê´ëÇб³ ÀÇ°ú´ëÇÐ ¼­¿ïÁß¾Óº´¿ø Áø´Üº´¸®Çб³½Ç

Abstract


Sarcoidosis, in general, has a low mortality rate. But cardiac sarcoidosis (CS) is a serious condition which may lead to death. Here, we report a rare case of CS that was treated by heart transplantation. A 47-year-old male had occasional syncopes and atypical chest pain. Ventricular tachycardia with right bundle branch block was noted by electrocardiogram. Multiple fixed myocardial perfusion defects in the interventricular septum and both the inferiorposterior ventricular walls were observed by thallium scan. Coronary angiography was unremarkable. Neither perihilar nor mediastinal lymphadenopathy was noted. The patient also suffered three times from tonic-clonic generalized seizures in 3 years, but no neurologic abnormalities were detected. The explanted heart displayed multiple white patches on the endomyocardial surface, measuring up to 8x7 cm. On microscopic examination, the lesion consisted of multiple well-formed and confluent granulomas with numerous scattered multinucleated giant cells, CD68-positive epithelioid histiocytes, and T-lymphocytes. Neither microorganisms nor foreign material was identified on special stain and culture study. It has been six months since the heart transplant, and the patient has been doing well.

Å°¿öµå

Cardiac sarcoidosis;Granuloma;Heart transplantation

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