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肝紫癜症复发性自发性肝内出血。

Recurrent spontaneous intrahepatic hemorrhage from peliosis hepatis.

作者信息

Hayward S R, Lucas C E, Ledgerwood A M

机构信息

Department of Surgery, Wayne State University, Detroit, Mich 48201.

出版信息

Arch Surg. 1991 Jun;126(6):782-3. doi: 10.1001/archsurg.1991.01410300128021.

Abstract

Peliosis hepatis is a rare and highly lethal liver lesion in which numerous blood-filled cavities or cystic spaces are dispersed throughout the hepatic parenchyma. The cause is unknown, although the condition is associated with several disease states and medications. Patients may present with hemorrhage, liver failure, the hepatorenal syndrome, cholestasis, or portal hypertension. We treated a patient who survived two separate hemorrhages from peliosis hepatis. The surgical intervention used, hepatic dearterialization, has allowed this patient to remain asymptomatic for 5 years.

摘要

肝紫癜是一种罕见且致死率很高的肝脏病变,其中大量充满血液的腔隙或囊性间隙散布于肝实质内。病因不明,尽管该病症与多种疾病状态及药物有关。患者可能出现出血、肝衰竭、肝肾综合征、胆汁淤积或门静脉高压。我们治疗了一名经历两次肝紫癜出血后存活下来的患者。所采用的手术干预措施,即肝动脉去血管化,使该患者5年来一直无症状。

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