肝切除标本中的合并肝细胞胆管癌:临床病理学分析

IF 0.8 4区 医学 Q4 PATHOLOGY Indian Journal of Pathology and Microbiology Pub Date : 2023-10-01 DOI:10.4103/ijpm.ijpm_357_22
Nayana Patil, Puja Sahai, Archana Rastogi, Namita Sharma, Saggere Muralikrishna Shasthry, Amar Mukund, Shalini Thapar Laroia, Guresh Kumar, Viniyendra Pamecha, Shiv Kumar Sarin
{"title":"肝切除标本中的合并肝细胞胆管癌:临床病理学分析","authors":"Nayana Patil, Puja Sahai, Archana Rastogi, Namita Sharma, Saggere Muralikrishna Shasthry, Amar Mukund, Shalini Thapar Laroia, Guresh Kumar, Viniyendra Pamecha, Shiv Kumar Sarin","doi":"10.4103/ijpm.ijpm_357_22","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Combined hepatocellular-cholangiocarcinoma (cHCC-CCA) is an uncommon form of primary liver carcinoma. It is heterogenous in terms of morphology, immunohistochemistry, radiology, and clinical features; making it a challenging entity for diagnosis.</p><p><strong>Aims: </strong>The purpose of the present study was to evaluate clinicopathological characteristics of patients with cHCC-CCA.</p><p><strong>Settings and design: </strong>Retrospective observational study.</p><p><strong>Materials and methods: </strong>The patients diagnosed with cHCC-CC were identified from hepatic surgical specimens and were evaluated.</p><p><strong>Statistical analysis: </strong>Survival was estimated as per Kaplan-Meier method.</p><p><strong>Results: </strong>Out of six patients, five had undergone resection while one had liver transplant. Five were male and one was female and the mean age was 52 years. Tumor markers revealed raised serum alfa-fetoprotein and CA19.9 in four and three patients, respectively. Five of the liver specimens were cirrhotic. Diagnosis was predominantly based on tumor morphology. All cases were of Allen and Lisa type B and cHCC-CCA as per WHO (2019) classification. Stem cell features <5% were noted in two cases. Immunohistochemistry for programmed death 1/programmed death ligand 1 (PD1/PDL1) was negative in both the hepatocellular and cholangiocellular components in all six cases. Mismatch repair (MMR) protein expression was retained in two and deficient in four cases. The median follow-up after surgery was 21.3 months (range, 5-46.2 months). Five patients had intrahepatic and/or extrahepatic recurrence on follow-up after surgery. The median recurrence-free survival was estimated at 13.1 months (95% CI 5.67-20.6). Three patients had received salvage treatment. The median overall survival was estimated at 20 months (95% CI 0-45.3).</p><p><strong>Conclusions: </strong>The present study highlights the role of morphology in the diagnosis of cHCC-CCA. The choice of locoregional and/or systemic therapy after surgery may be individualized based on the clinicopathological characteristics.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":0.8000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Combined hepatocellular cholangiocarcinoma in hepatectomy specimens: A clinicopathologic analysis.\",\"authors\":\"Nayana Patil, Puja Sahai, Archana Rastogi, Namita Sharma, Saggere Muralikrishna Shasthry, Amar Mukund, Shalini Thapar Laroia, Guresh Kumar, Viniyendra Pamecha, Shiv Kumar Sarin\",\"doi\":\"10.4103/ijpm.ijpm_357_22\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Combined hepatocellular-cholangiocarcinoma (cHCC-CCA) is an uncommon form of primary liver carcinoma. It is heterogenous in terms of morphology, immunohistochemistry, radiology, and clinical features; making it a challenging entity for diagnosis.</p><p><strong>Aims: </strong>The purpose of the present study was to evaluate clinicopathological characteristics of patients with cHCC-CCA.</p><p><strong>Settings and design: </strong>Retrospective observational study.</p><p><strong>Materials and methods: </strong>The patients diagnosed with cHCC-CC were identified from hepatic surgical specimens and were evaluated.</p><p><strong>Statistical analysis: </strong>Survival was estimated as per Kaplan-Meier method.</p><p><strong>Results: </strong>Out of six patients, five had undergone resection while one had liver transplant. Five were male and one was female and the mean age was 52 years. Tumor markers revealed raised serum alfa-fetoprotein and CA19.9 in four and three patients, respectively. Five of the liver specimens were cirrhotic. Diagnosis was predominantly based on tumor morphology. All cases were of Allen and Lisa type B and cHCC-CCA as per WHO (2019) classification. Stem cell features <5% were noted in two cases. Immunohistochemistry for programmed death 1/programmed death ligand 1 (PD1/PDL1) was negative in both the hepatocellular and cholangiocellular components in all six cases. Mismatch repair (MMR) protein expression was retained in two and deficient in four cases. The median follow-up after surgery was 21.3 months (range, 5-46.2 months). Five patients had intrahepatic and/or extrahepatic recurrence on follow-up after surgery. The median recurrence-free survival was estimated at 13.1 months (95% CI 5.67-20.6). Three patients had received salvage treatment. The median overall survival was estimated at 20 months (95% CI 0-45.3).</p><p><strong>Conclusions: </strong>The present study highlights the role of morphology in the diagnosis of cHCC-CCA. The choice of locoregional and/or systemic therapy after surgery may be individualized based on the clinicopathological characteristics.</p>\",\"PeriodicalId\":13488,\"journal\":{\"name\":\"Indian Journal of Pathology and Microbiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2023-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Pathology and Microbiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.4103/ijpm.ijpm_357_22\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PATHOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Pathology and Microbiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4103/ijpm.ijpm_357_22","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:肝细胞胆管癌(cHCC-CCA)是一种不常见的原发性肝癌。本研究旨在评估 cHCC-CCA 患者的临床病理特征:资料和方法:回顾性观察研究:从肝脏手术标本中确定并评估确诊为 cHCC-CC 的患者:统计分析:根据 Kaplan-Meier 法估算生存率:六名患者中,五人接受了切除手术,一人进行了肝移植。五名患者为男性,一名为女性,平均年龄为 52 岁。肿瘤标志物显示,4 名患者血清中的甲胎蛋白升高,3 名患者血清中的 CA19.9 升高。其中五例肝脏标本为肝硬化。诊断主要依据肿瘤形态。根据世界卫生组织(2019年)的分类,所有病例均为Allen和Lisa B型及cHCC-CCA。干细胞特征 结论:本研究强调了形态学在 cHCC-CCA 诊断中的作用。术后局部和/或全身治疗的选择可根据临床病理特征进行个体化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Combined hepatocellular cholangiocarcinoma in hepatectomy specimens: A clinicopathologic analysis.

Background: Combined hepatocellular-cholangiocarcinoma (cHCC-CCA) is an uncommon form of primary liver carcinoma. It is heterogenous in terms of morphology, immunohistochemistry, radiology, and clinical features; making it a challenging entity for diagnosis.

Aims: The purpose of the present study was to evaluate clinicopathological characteristics of patients with cHCC-CCA.

Settings and design: Retrospective observational study.

Materials and methods: The patients diagnosed with cHCC-CC were identified from hepatic surgical specimens and were evaluated.

Statistical analysis: Survival was estimated as per Kaplan-Meier method.

Results: Out of six patients, five had undergone resection while one had liver transplant. Five were male and one was female and the mean age was 52 years. Tumor markers revealed raised serum alfa-fetoprotein and CA19.9 in four and three patients, respectively. Five of the liver specimens were cirrhotic. Diagnosis was predominantly based on tumor morphology. All cases were of Allen and Lisa type B and cHCC-CCA as per WHO (2019) classification. Stem cell features <5% were noted in two cases. Immunohistochemistry for programmed death 1/programmed death ligand 1 (PD1/PDL1) was negative in both the hepatocellular and cholangiocellular components in all six cases. Mismatch repair (MMR) protein expression was retained in two and deficient in four cases. The median follow-up after surgery was 21.3 months (range, 5-46.2 months). Five patients had intrahepatic and/or extrahepatic recurrence on follow-up after surgery. The median recurrence-free survival was estimated at 13.1 months (95% CI 5.67-20.6). Three patients had received salvage treatment. The median overall survival was estimated at 20 months (95% CI 0-45.3).

Conclusions: The present study highlights the role of morphology in the diagnosis of cHCC-CCA. The choice of locoregional and/or systemic therapy after surgery may be individualized based on the clinicopathological characteristics.

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
CiteScore
1.20
自引率
0.00%
发文量
422
审稿时长
1 months
期刊介绍: The journal will cover studies related to pathology including morbid anatomy, surgical pathology, clinical pathology, diagnostic cytopathology including gynecologic cytology and aspiration cytology, hematology including immuno-hematology and medical microbiology. The journal gives preference to clinically oriented studies over experimental and animal studies. The Journal would publish peer-reviewed original research papers, case reports, systematic reviews, meta-analysis, letters to the editor and brief communications. Review articles on current topics usually are invited by the editor.
期刊最新文献
Low-grade fibromyxoid sarcoma of the maxilla: A diagnosis not to be missed Ischemic fasciitis scalp-unusual presentation and location. Post-mortem detection of a calcifying fibrous pseudotumor at a rare site-A case report. Mesenchymal chondrosarcoma with rhabdomyoblastic differentiation: A malignant round cell tumor with enigmatic immunohistochemical profile. Burnt out testicular tumor - A case report.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1