Fan Jerry, Le Phuong Tram N, Ellington Tyler, Jones Billy D
Department of Internal Medicine, Baylor Scott & White HospitalTempleTexas.
Department of Cardiology, Baylor Scott & White HospitalTempleTexas.
Proc (Bayl Univ Med Cent). 2019 Jun 5;32(3):385-386. doi: 10.1080/08998280.2019.1608623. eCollection 2019 Jul.
Cardiac lipomas are rare and usually benign tumors that often remain asymptomatic throughout one's lifetime. We report a case of a 60-year-old man with a cardiac lipoma diagnosed early in childhood. However, due to the lack of surgical expertise in rural India, the lipoma was not removed. After moving to the United States, he received irregular follow-up with serial chest x-ray and computed tomography, which demonstrated an enlarging lipomatous mass occupying the pericardial space. After remaining asymptomatic for more than 37 years, he presented to the hospital with dyspnea. He underwent a surgical resection but, unfortunately, given the extension of the mass into multiple critical portions of the heart, he ultimately died.
心脏脂肪瘤是罕见的,通常为良性肿瘤,常常在人的一生中都无症状。我们报告一例60岁男性,其心脏脂肪瘤在儿童早期被诊断出来。然而,由于印度农村地区缺乏手术专业技术,该脂肪瘤未被切除。搬到美国后,他接受了胸部X线和计算机断层扫描的不定期随访,结果显示一个脂肪瘤样肿块在增大,占据心包间隙。在37年多无症状后,他因呼吸困难入院。他接受了手术切除,但不幸的是,由于肿块延伸至心脏的多个关键部位,他最终死亡。