首页> 外文期刊>Zeitschrift fur Gastroenterologie >Cystic echinococcosis and hepatocellular carcinoma - A coincidence? A case report [Zystische Echinokokkose und hepatozellul?res Karzinom - zuf?llige Koinzidenz? Ein Fallbericht]
【24h】

Cystic echinococcosis and hepatocellular carcinoma - A coincidence? A case report [Zystische Echinokokkose und hepatozellul?res Karzinom - zuf?llige Koinzidenz? Ein Fallbericht]

机译:囊性棘球cc虫病和肝细胞癌-巧合吗?病例报告[囊性棘球co病和肝细胞癌-偶然巧合?病例报告]

获取原文
获取原文并翻译 | 示例
           

摘要

Introduction: The coincidence of echinococcosis and hepatocellular carcinoma (HCC) is quite rare. We report the case of a 45-year-old man who was admitted to our hospital because of abdominal pain in the right upper quadrant and jaundice. Clinical features and diagnostics: There was no history of weight loss or fever. No abdominal mass was palpable. The laboratory reports showed increased transaminase levels. Ultrasonography revealed an inhomogenous, cystic lesion measuring 6 cm in diameter in the segments VI and VII. Serology for echinococcosis was negative, alpha-fetoprotein (AFP) was considerably increased. CT scan showed a solid mass of 3,7 cm in diameter adjacent to the cystic lesion. Therapy and course: Anthelminthic therapy with albendazole caused a massive increase of cholestasis parameters and treatment had to be stopped. The simultaneous occurrence of serologically negative cystic echinococcosis and HCC was suspected and partial liver resection was performed. Histological examination confirmed both diagnoses and tumor resection in healthy tissue. 5 months after resection CT scan showed multicentric HCC affecting the whole liver. Palliative therapy with sorafenib was established. Discussion: The coincidence of HCC and cystic echinococcosis in the non-cirrhotic liver of a young man is a rare event. Despite resection in healthy tissue multicentric HCC was diagnosed 5 months later. Only few cases of simultaneous occurrence of HCC and echinococcosis have been published so far. Some authors considered echinococcosis as a trigger for HCC. A causal link between both entities has not been demonstrated until now.
机译:简介:棘球co虫病和肝细胞癌(HCC)的重合非常罕见。我们报告了一个因右上腹和黄疸腹痛入院的45岁男子的病例。临床特征和诊断:没有减肥或发烧史。没有明显的腹部肿块。实验室报告显示转氨酶水平升高。超声检查显示,VI和VII节的直径不超过6 cm的囊性病变不均匀。棘球菌病血清学阴性,甲胎蛋白(AFP)显着增加。 CT扫描显示邻近囊性病变的直径为3,7 cm的实性肿块。治疗方法和疗程:用阿苯达唑进行驱虫药治疗会导致胆汁淤积参数大量增加,因此必须停止治疗。怀疑血清学阴性的囊性棘球co虫病和HCC同时发生,并进行了部分肝切除。组织学检查证实了健康组织的诊断和肿瘤切除。切除后5个月,CT扫描显示多中心HCC影响整个肝脏。建立了索拉非尼的姑息治疗。讨论:年轻人非肝硬化性肝癌和囊性棘球co虫病的巧合是罕见的。尽管在健康组织中进行了切除,但5个月后仍诊断出多中心HCC。迄今为止,只有少数几例同时发生肝癌和棘球co虫病的病例被发表。一些作者认为棘球病是肝癌的诱因。到目前为止,尚未证明两个实体之间的因果关系。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号