Kim Hyun Jung, Lee Gyeong Won, Park Dong Jun, Lee Jong Deog, Chang Se Ho
Department of Internal Medicine, Eulji University, Daejeon, Korea.
Yonsei Med J. 2005 Jun 30;46(3):435-8. doi: 10.3349/ymj.2005.46.3.435.
Spontaneous splenic rupture (SSR) in a patient undergoing hemodialysis has been described as an extremely rare and potentially fatal complication. We report here spontaneous splenic rupture in a 52-year-old woman undergoing regular hemodialysis for end-stage renal disease (ESRD). She complained of colicky abdominal pain in the left upper quadrant area and dizziness when she assumed an upright posture. Her vital signs revealed low blood pressure and tachycardia, which was suggestive of hypovolemic shock. Abdomen CT scan showed splenic hematoma and hemoperitoneum. However, she had no history of any event triggering the splenic rupture. An exploratory laparotomy showed a ruptured spleen and an emergency splenectomy was performed. We suggest that spontaneous spleen rupture may be attributed to uremic coagulopathy and heparin-induced coagulopathy.
接受血液透析的患者发生自发性脾破裂(SSR)被描述为一种极其罕见且可能致命的并发症。我们在此报告一名52岁因终末期肾病(ESRD)接受定期血液透析的女性发生自发性脾破裂的病例。她主诉左上腹绞痛,直立时头晕。她的生命体征显示血压低和心动过速,提示低血容量性休克。腹部CT扫描显示脾血肿和腹腔积血。然而,她没有任何引发脾破裂的事件史。剖腹探查显示脾脏破裂,并进行了急诊脾切除术。我们认为自发性脾破裂可能归因于尿毒症性凝血病和肝素诱导的凝血病。