肺泡包虫病模拟肝门周围胆管癌导致肝移植1例报告。

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
Hrvoje Premec, Mislav Barišić-Jaman, Petra Dinjar Kujundžić, Nikola Sobočan, Maja Mijić, Miloš Lalovac, Frane Paštrović, Vid Matišić, Ivica Grgurević, Tajana Filipec-Kanižaj
{"title":"肺泡包虫病模拟肝门周围胆管癌导致肝移植1例报告。","authors":"Hrvoje Premec, Mislav Barišić-Jaman, Petra Dinjar Kujundžić, Nikola Sobočan, Maja Mijić, Miloš Lalovac, Frane Paštrović, Vid Matišić, Ivica Grgurević, Tajana Filipec-Kanižaj","doi":"10.12659/AJCR.948414","DOIUrl":null,"url":null,"abstract":"<p><p>BACKGROUND Alveolar echinococcosis (AE) is a slowly progressive parasitic disease that primarily affects the liver and resembles primary or secondary liver neoplasms. Differentiating AE from other primary or secondary liver malignancies is of paramount importance, due to differing therapeutic approaches. The disease is uncommon in developed countries. Initial extrahepatic manifestation mimicking a primary biliary neoplasm is extremely rare. A broad differential diagnosis and low disease prevalence make the diagnosis of primary biliary AE extremely challenging. CASE REPORT We present a 32-year-old male patient with perihilar AE and no significant past medical history. The initial clinical presentation and radiological findings were compatible with the diagnosis of perihilar cholangiocarcinoma (Klatskin tumor). The patient subsequently underwent extensive invasive diagnostic procedures, including endoscopic ultrasound and endoscopic retrograde cholangiopancreatography, which led to choledochal perforation and biliary leakage, necessitating urgent surgical procedure, along with exploration, evacuation of enlarged lymph nodes, and subsequent histopathological examination. None of the procedures provided definitive evidence of malignancy. Only an ultrasound-guided percutaneous biopsy followed by histopathological examination revealed AE. Albendazole treatment and close follow-up were initiated. Subsequently, the patient experienced recurrent episodes of acute cholangitis. Recurrent cholangitis and perihilar biliary involvement, precluding radical surgical resection, necessitated liver transplantation. Ultimately, the patient underwent orthotopic liver transplantation from a brain-dead donor, with a favorable outcome. CONCLUSIONS Liver transplantation is a definitive treatment option for selected patients with perihilar liver involvement precluding radical resection of parasitic mass and recurrent episodes of acute cholangitis.</p>","PeriodicalId":39064,"journal":{"name":"American Journal of Case Reports","volume":"26 ","pages":"e948414"},"PeriodicalIF":0.7000,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12459208/pdf/","citationCount":"0","resultStr":"{\"title\":\"Alveolar Echinococcosis Mimicking Perihilar Cholangiocarcinoma Leading to Liver Transplant: A Case Report.\",\"authors\":\"Hrvoje Premec, Mislav Barišić-Jaman, Petra Dinjar Kujundžić, Nikola Sobočan, Maja Mijić, Miloš Lalovac, Frane Paštrović, Vid Matišić, Ivica Grgurević, Tajana Filipec-Kanižaj\",\"doi\":\"10.12659/AJCR.948414\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>BACKGROUND Alveolar echinococcosis (AE) is a slowly progressive parasitic disease that primarily affects the liver and resembles primary or secondary liver neoplasms. Differentiating AE from other primary or secondary liver malignancies is of paramount importance, due to differing therapeutic approaches. The disease is uncommon in developed countries. Initial extrahepatic manifestation mimicking a primary biliary neoplasm is extremely rare. A broad differential diagnosis and low disease prevalence make the diagnosis of primary biliary AE extremely challenging. CASE REPORT We present a 32-year-old male patient with perihilar AE and no significant past medical history. The initial clinical presentation and radiological findings were compatible with the diagnosis of perihilar cholangiocarcinoma (Klatskin tumor). The patient subsequently underwent extensive invasive diagnostic procedures, including endoscopic ultrasound and endoscopic retrograde cholangiopancreatography, which led to choledochal perforation and biliary leakage, necessitating urgent surgical procedure, along with exploration, evacuation of enlarged lymph nodes, and subsequent histopathological examination. None of the procedures provided definitive evidence of malignancy. Only an ultrasound-guided percutaneous biopsy followed by histopathological examination revealed AE. Albendazole treatment and close follow-up were initiated. Subsequently, the patient experienced recurrent episodes of acute cholangitis. Recurrent cholangitis and perihilar biliary involvement, precluding radical surgical resection, necessitated liver transplantation. Ultimately, the patient underwent orthotopic liver transplantation from a brain-dead donor, with a favorable outcome. CONCLUSIONS Liver transplantation is a definitive treatment option for selected patients with perihilar liver involvement precluding radical resection of parasitic mass and recurrent episodes of acute cholangitis.</p>\",\"PeriodicalId\":39064,\"journal\":{\"name\":\"American Journal of Case Reports\",\"volume\":\"26 \",\"pages\":\"e948414\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2025-09-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12459208/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.12659/AJCR.948414\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12659/AJCR.948414","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

摘要

肺泡包虫病(AE)是一种缓慢进展的寄生虫病,主要影响肝脏,类似原发性或继发性肝脏肿瘤。由于治疗方法不同,区分AE与其他原发性或继发性肝脏恶性肿瘤至关重要。这种疾病在发达国家并不常见。最初的肝外表现与原发性胆道肿瘤相似是极为罕见的。广泛的鉴别诊断和低发病率使得原发性胆道AE的诊断极具挑战性。病例报告:我们报告一位32岁男性患者,患有门周AE,既往无明显病史。最初的临床表现和影像学表现符合门周胆管癌(克拉特金肿瘤)的诊断。患者随后接受了广泛的侵入性诊断,包括内镜超声和内镜逆行胆管造影,导致胆总管穿孔和胆漏,需要紧急手术治疗,同时探查、清除肿大的淋巴结,并进行组织病理学检查。所有的手术都没有提供恶性肿瘤的明确证据。只有超声引导下的经皮活检和组织病理学检查显示AE。开始阿苯达唑治疗并密切随访。随后,患者反复发作急性胆管炎。复发性胆管炎和肝门周围胆道受累,无法根治性手术切除,需要肝移植。最终,患者接受了脑死亡供体的原位肝移植,结果良好。结论肝移植是肝门周围受损伤患者排除寄生虫肿物根治性切除和急性胆管炎复发的最终治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alveolar Echinococcosis Mimicking Perihilar Cholangiocarcinoma Leading to Liver Transplant: A Case Report.

BACKGROUND Alveolar echinococcosis (AE) is a slowly progressive parasitic disease that primarily affects the liver and resembles primary or secondary liver neoplasms. Differentiating AE from other primary or secondary liver malignancies is of paramount importance, due to differing therapeutic approaches. The disease is uncommon in developed countries. Initial extrahepatic manifestation mimicking a primary biliary neoplasm is extremely rare. A broad differential diagnosis and low disease prevalence make the diagnosis of primary biliary AE extremely challenging. CASE REPORT We present a 32-year-old male patient with perihilar AE and no significant past medical history. The initial clinical presentation and radiological findings were compatible with the diagnosis of perihilar cholangiocarcinoma (Klatskin tumor). The patient subsequently underwent extensive invasive diagnostic procedures, including endoscopic ultrasound and endoscopic retrograde cholangiopancreatography, which led to choledochal perforation and biliary leakage, necessitating urgent surgical procedure, along with exploration, evacuation of enlarged lymph nodes, and subsequent histopathological examination. None of the procedures provided definitive evidence of malignancy. Only an ultrasound-guided percutaneous biopsy followed by histopathological examination revealed AE. Albendazole treatment and close follow-up were initiated. Subsequently, the patient experienced recurrent episodes of acute cholangitis. Recurrent cholangitis and perihilar biliary involvement, precluding radical surgical resection, necessitated liver transplantation. Ultimately, the patient underwent orthotopic liver transplantation from a brain-dead donor, with a favorable outcome. CONCLUSIONS Liver transplantation is a definitive treatment option for selected patients with perihilar liver involvement precluding radical resection of parasitic mass and recurrent episodes of acute cholangitis.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信