A Case of Hepatic Angiosarcoma
10.12376/j.issn.2097-0501.2025.02.015
- VernacularTitle:肝血管肉瘤一例
- Author:
Linhao ZHANG
1
;
Chengwei TANG
1
;
Zhiyin HUANG
1
Author Information
1. 四川大学华西医院消化内科,成都 610041
- Publication Type:Journal Article
- Keywords:
hepatic angiosarcoma;
disseminated intravascular coagulation;
hepatic sinusoidal obstruction syndrome;
Ka-sabach-Merritt phenomenon
- From:
JOURNAL OF RARE DISEASES
2025;4(2):263-268
- CountryChina
- Language:Chinese
-
Abstract:
Hepatic angiosarcoma is a rare,highly malignant tumor originating from liver blood vessels or lymphatic vessels.Its clinical manifestations and imaging examinations are not specific,and pathological biopsy is needed to confirm the diagnosis.This article reports a 47-year-old male patient with hepatic angiosarcoma,who has clinical manifestations of abdominal pain,jaundice,and disseminated intravascular coagulation.The CT and MRI findings of this patient are similar to hepatic sinusoidal obstruction syndrome.Relevant literature on hepatic angiosarcoma in recent years was reviewed.The manifestations,diagnosis and treatment of hepatic angiosarcoma were summarized to improve clinicians'understanding of the disease.
