原发性肝上皮样血管内皮瘤1例。

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Jing-Rui Wang, Qi-Jun Yang, Bei Lu, Yang Cai, Jun-Jie Yin
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引用次数: 0

摘要

上皮样血管内皮瘤是一种起源于血管的低级别恶性肿瘤。肝上皮样血管内皮瘤(HEHE)的罕见性使其诊断和治疗具有挑战性。我们报告一位69岁的女性患者,她患有HEHE,主诉腹胀疼痛并头晕和食欲不振半个多月。上腹部增强ct显示肝脏多发占位性病变。彩色超声穿刺病理结果提示HEHE。我们根据患者的病情和选择进行了经导管动脉化疗栓塞和相关检查。我们对患者进行了5年的随访,发现她出现了复发性肝内肿瘤转移。使用anlotinib治疗3个月后再次进行计算机断层扫描,肿瘤未显示任何进展。HEHE是一种相对罕见的来源于血管内皮细胞的肝脏恶性肿瘤,发病率低,临床表现不典型,诊断困难,只能通过病理结果确诊。目前,应根据患者的具体情况选择合适的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary hepatic epithelioid hemangioendothelioma: a case report.

Epithelioid hemangioendothelioma is a low-grade malignant tumor of vascular origin. The rarity of hepatic epithelioid hemangioendothelioma (HEHE) makes the diagnosis and treatment of this entity challenging. We report a case of a 69-year-old female patient who suffered from HEHE and complained of abdominal distension pain with dizziness and appetite loss for more than half a month. Enhanced computed tomography of the upper abdomen indicated multiple space-occupying lesions in the liver. The pathological results of color ultrasound puncture suggested HEHE. We performed transcatheter arterial chemoembolization and relevant examinations according to the patient's condition and their choice. We followed the patient for 5 years and found that she developed recurrent intrahepatic metastasis of the tumor. Computed tomography was performed again after 3 months of treatment with anlotinib and the tumor did not show any progression. HEHE is a relatively rare hepatic malignant tumor derived from vascular endothelial cells, with a low incidence, atypical clinical manifestations, and a difficult diagnosis that can only be confirmed with pathological results. Currently, appropriate treatment methods should be selected according to the specific conditions of the patient.

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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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