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腹膜和大网膜产甲胎蛋白的肝样腺癌:一例报告及文献复习

AFP-producing hepatoid adenocarcinoma (HAC) of peritoneum and omentum: a case report and literature review.

作者信息

Zou Man, Li Yanhui, Dai Yuhong, Sun Li, Huang Tingting, Yuan Xianglin, Qiu Hong

机构信息

Department of Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.

Department of Cardiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.

出版信息

Onco Targets Ther. 2019 Sep 18;12:7649-7654. doi: 10.2147/OTT.S216501. eCollection 2019.

Abstract

Hepatoid adenocarcinoma (HAC) is a group of neoplasms with features resembling hepatocellular carcinoma. The stomach is the most commonly affected organ among the reported primary sites. We report the case of a 28-year-old man with chronic hepatitis B and a complaint of abdominal distension. The patient was examined by PET-CT and magnetic resonance imaging (MRI), which showed diffuse thickening of the peritoneum and omentum but no mass was found in the liver. Pathological examination of a biopsy of the omental nodules was consistent with moderately differentiated hepatocellular carcinoma (HCC); thus, a diagnosis of HAC of the peritoneum and omentum was established. The patient received a chemotherapy regimen consisting of oxaliplatin and capecitabine and gained remarkable effects as the AFP level dropped significantly, and the tumour nearly disappeared. When the patient shifted to the standard multikinase inhibitors, Sorafenib or Lenvatinib, both treatments were ineffective. HAC is a heterogeneous group of prognostically unfavourable tumours mimicking the histological appearance of HCC, and the treatment outcomes are still unclear.

摘要

肝样腺癌(HAC)是一组具有类似肝细胞癌特征的肿瘤。在已报道的原发部位中,胃是最常受累的器官。我们报告一例28岁慢性乙型肝炎男性患者,主诉腹胀。患者接受了PET-CT和磁共振成像(MRI)检查,结果显示腹膜和大网膜弥漫性增厚,但肝脏未发现肿块。大网膜结节活检的病理检查结果与中度分化肝细胞癌(HCC)一致,因此确诊为腹膜和大网膜HAC。患者接受了由奥沙利铂和卡培他滨组成的化疗方案,效果显著,甲胎蛋白水平显著下降,肿瘤几乎消失。当患者改用标准多激酶抑制剂索拉非尼或仑伐替尼时,两种治疗均无效。HAC是一组预后不良的异质性肿瘤,其组织学表现类似HCC,治疗结果仍不明确。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8f8/6756369/8c35f3b6ea43/OTT-12-7649-g0001.jpg

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