Hepatic epithelioid hemangioendothelioma simulating liver metastasis: A case report

被引:1
|
作者
Serji, Badr [1 ,2 ]
Ramdani, Abdelbassir [1 ,2 ]
Mirali, Houda [2 ,3 ]
Bouhout, Tariq [1 ,2 ]
Bennani, Amal [2 ,4 ]
El Harroudi, Tijani [1 ,2 ]
机构
[1] Mohammed VI Univ Hosp, Reg Oncol Ctr, Surg Oncol Dept, Oujda, Morocco
[2] Mohammed First Univ Oujda, Fac Med & Pharm Oujda, Oujda, Morocco
[3] Mohammed VI Univ Hosp, Radiol Dept, Oujda, Morocco
[4] Mohammed VI Univ Hosp, Pathol Dept, Oujda, Morocco
来源
ANNALS OF MEDICINE AND SURGERY | 2021年 / 70卷
关键词
Hepatic epithelioid hemangioendothelioma; Case report; Hepatobiliary surgery; TRANSPLANTATION; CT;
D O I
10.1016/j.amsu.2021.102885
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Hepatic epithelioid hemangioendothelioma (HEHE) is a rare tumor of vascular origin. Liver involvement is often multinodular simulating metastases. Herein, we report a rare case of HEHE mimicking liver metastases in a female patient. Case presentation: A 43-years-old female patient, presented with complaints of pain in the right upper quadrant. Laboratory tests were all within the normal range. Abdominal ultrasound revealed multiple heterogeneous hypoechoic liver lesions. A thoracic and abdominopelvic computed tomography showed bilateral pulmonary micronodules with multiple hypodense hepatic nodules involving both lobes. Percutaneous ultrasound-guided biopsy with pathological study and immunohistochemistry staining revealed the diagnosis of hepatic epithelioid hemangioendothelioma. Discussion: HEHE usually involves both liver lobes with three radiological presentations: single nodular, multiple nodular, or diffuse types, the diffuse type reflects an advanced stage. 3/4 of the cases are initially misdiagnosed as liver metastases or primary liver tumors. The pathological study with the immunochemistry stainings confirms the diagnosis. There is no standard treatment for HEHE due to its rarity and lack of prospective randomized studies. Conclusion: HEHE is a rare tumor of vascular origin of unknown etiology with malignant potential and unpredictable course. The therapeutic management of this rare condition is not codified and is discussed on a case-by-case basis. Surgical treatment remains the best option with an excellent outcome.
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页数:3
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