Department of Internal Medicine, Kaiser Permanente San Francisco Medical Center, San Francisco, CA.
Perm J. 2020 Nov;24:1-4. doi: 10.7812/TPP/19.132.
Liver hematoma is an uncommon feature of Ehlers-Danlos syndrome (EDS) type IV. The limited literature that exists to guide management does not establish a standard of care.
A 26-year-old man presented with acute abdominal pain caused by a large, spontaneous liver hematoma. Invasive prophylactic arterial embolization was done twice, but surgical evacuation was not offered because of concern for poor healing and brittle vasculature, later diagnosed as symptoms of the patient's EDS type IV. During hospitalization the patient died of spontaneous intracerebral and intra-abdominal hemorrhaging.
This case illustrates a nonsurgical management option for spontaneous liver hematoma in a patient with EDS type IV. An interdisciplinary team should help guide care, including consideration of invasive procedures such as arterial embolization and surgery. Patient and family education, genetic testing, and timely medical record documentation may reduce the morbidity and mortality of patients with this syndrome.
肝血肿是埃勒斯-当洛斯综合征(EDS)IV 型的一种罕见特征。现有的有限文献并不能为管理提供标准。
一名 26 岁男性因自发性大肝血肿引起急性腹痛。进行了两次有创预防性动脉栓塞,但因担心愈合不良和脆弱的脉管系统,未提供手术清除,后来被诊断为患者 EDS IV 型的症状。住院期间,患者死于自发性颅内和腹腔内出血。
本病例说明了 EDS IV 型患者自发性肝血肿的一种非手术治疗选择。多学科团队应有助于指导治疗,包括考虑动脉栓塞和手术等有创性操作。患者和家属教育、基因检测以及及时的病历记录可能会降低该综合征患者的发病率和死亡率。