Paşaoğlu I, Demircin M, Ozkutlu S, Bozer A Y
Department of Thoracic and Cardiovascular Surgery, Hacettepe University, Ankara, Turkey.
Jpn Heart J. 1991 Mar;32(2):263-6. doi: 10.1536/ihj.32.263.
Cardiac myxomas are extremely rare in infancy. We report a case of right atrial myxoma in a 35-day-old male infant (with cyanosis and convulsions). Echocardiography was carried out and a diagnosis of right atrial myxoma was made. Open heart surgery was performed using cardiopulmonary bypass and a 2.5 X 3.0 cm mass was removed. The patient's postoperative course was uneventful. To our knowledge there is no previously reported case of right atrial myxoma in such a young infant which was operated on successfully.
心脏黏液瘤在婴儿期极为罕见。我们报告一例35日龄男婴(伴有青紫和惊厥)的右心房黏液瘤病例。进行了超声心动图检查并诊断为右心房黏液瘤。采用体外循环进行了心脏直视手术,切除了一个2.5×3.0厘米的肿块。患者术后恢复顺利。据我们所知,此前尚无如此年幼婴儿成功接受手术治疗的右心房黏液瘤病例报道。