• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肝肿瘤罕见且缺乏典型临床症状:四例病例报告

Rare and lacking typical clinical symptoms of liver tumors: Four case reports.

作者信息

Zhao Yun, Bie Yu-Kun, Zhang Guang-Ya, Feng Yi-Bin, Wang Feng

机构信息

Department of Hepatobiliary Surgery, Ankang Central Hospital, Ankang 725000, Shaanxi Province, China.

出版信息

World J Gastrointest Oncol. 2024 Oct 15;16(10):4264-4273. doi: 10.4251/wjgo.v16.i10.4264.

DOI:10.4251/wjgo.v16.i10.4264
PMID:39473954
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11514678/
Abstract

BACKGROUND

Rare liver tumors (RLTs) have an extremely low likelihood of forming, and some have been recorded only in isolated cases. The lack of normal clinical symptoms in RLTs makes preoperative diagnosis extremely challenging, which results in frequent misinterpretation. The present case report helps enhance our ability to recognize and treat uncommon liver tumor disorders.

CASE SUMMARY

We describe four distinct examples of rare liver tumor diseases. These cases were all true cases with no conventional clinical signs or imaging findings. In all patients, hepatic occupancy was discovered on physical examination, which raised the preoperative suspicion of hepatic cancer. All tumors were surgically removed, and postoperative histology and immunohistochemistry were performed to confirm the diagnosis. The first patient had primary hepatic fibrosarcoma. The second case involved a primary hepatic neuroendocrine tumors. These two patients had malignant liver tumors, and both had extremely satisfactory surgical outcomes. The third case involved focal hepatic steatosis, and the fourth case involved a single necrotic nodule in the liver. These two patients had benign liver tumors, but they had already undergone surgery and did not require any postoperative care.

CONCLUSION

The number of patients with RLTs is small, and the clinical and imaging results are vague. Preoperative diagnosis is challenging, and patients are sometimes mistakenly diagnosed with liver cancer, which leads to unnecessary surgical therapy in certain individuals.

摘要

背景

罕见肝肿瘤(RLTs)形成的可能性极低,有些仅在个别病例中被记录。RLTs缺乏正常临床症状,这使得术前诊断极具挑战性,常导致误诊。本病例报告有助于提高我们识别和治疗罕见肝肿瘤疾病的能力。

病例总结

我们描述了四个罕见肝肿瘤疾病的不同实例。这些病例均为真实病例,无传统临床体征或影像学表现。所有患者在体格检查时均发现肝脏占位,这增加了术前对肝癌的怀疑。所有肿瘤均通过手术切除,并进行术后组织学和免疫组化检查以确诊。第一例患者患有原发性肝纤维肉瘤。第二例涉及原发性肝神经内分泌肿瘤。这两名患者患有恶性肝肿瘤,且手术效果都非常令人满意。第三例涉及局灶性肝脂肪变性,第四例涉及肝脏单个坏死结节。这两名患者患有良性肝肿瘤,但他们已经接受了手术,无需任何术后护理。

结论

RLTs患者数量较少,临床和影像学结果不明确。术前诊断具有挑战性,患者有时会被误诊为肝癌,这导致某些个体接受了不必要的手术治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7819/11514678/360a50d48446/WJGO-16-4264-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7819/11514678/851853b46c7e/WJGO-16-4264-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7819/11514678/bae170af82a8/WJGO-16-4264-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7819/11514678/fd40908533eb/WJGO-16-4264-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7819/11514678/360a50d48446/WJGO-16-4264-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7819/11514678/851853b46c7e/WJGO-16-4264-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7819/11514678/bae170af82a8/WJGO-16-4264-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7819/11514678/fd40908533eb/WJGO-16-4264-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7819/11514678/360a50d48446/WJGO-16-4264-g004.jpg

相似文献

1
Rare and lacking typical clinical symptoms of liver tumors: Four case reports.肝肿瘤罕见且缺乏典型临床症状:四例病例报告
World J Gastrointest Oncol. 2024 Oct 15;16(10):4264-4273. doi: 10.4251/wjgo.v16.i10.4264.
2
Rare benign liver tumors that require differentiation from hepatocellular carcinoma: focus on diagnosis and treatment.罕见的良性肝脏肿瘤,需要与肝细胞癌相鉴别:重点在于诊断与治疗。
J Cancer Res Clin Oncol. 2023 Jul;149(7):2843-2854. doi: 10.1007/s00432-022-04169-w. Epub 2022 Jul 5.
3
[Benign liver tumors].[良性肝脏肿瘤]
J Chir (Paris). 2001 Feb;138(1):19-26.
4
Fetal and neonatal hepatic tumors.胎儿及新生儿肝脏肿瘤。
J Pediatr Surg. 2007 Nov;42(11):1797-803. doi: 10.1016/j.jpedsurg.2007.07.047.
5
Primary hepatic neuroendocrine tumor: Five cases with different preoperative diagnoses.原发性肝神经内分泌肿瘤:5例术前诊断不同的病例。
Turk J Gastroenterol. 2012 Jun;23(3):272-8. doi: 10.4318/tjg.2012.0465.
6
Primary Hepatic Neuroendocrine Carcinoma with Metastasis to the Mesentery: A Case Report.原发性肝神经内分泌癌伴肠系膜转移:一例报告
Case Rep Oncol. 2023 Aug 22;16(1):681-697. doi: 10.1159/000533199. eCollection 2023 Jan-Dec.
7
An Interesting Case of Hepatic Adrenocortical Carcinoma.肝肾上腺皮质癌的一个有趣病例
Acta Med Indones. 2018 Jul;50(3):257-259.
8
Hepatic surgery for metastases from neuroendocrine tumors.神经内分泌肿瘤肝转移的肝手术治疗
Surg Oncol Clin N Am. 2003 Jan;12(1):231-42. doi: 10.1016/s1055-3207(02)00076-5.
9
Spontaneous hepatic rupture during late pregnancy in a patient with solitary necrotic nodule of the liver: A case report.肝孤立性坏死结节患者妊娠晚期自发性肝破裂:一例报告
Front Med (Lausanne). 2022 Oct 20;9:936006. doi: 10.3389/fmed.2022.936006. eCollection 2022.
10
Case Report: Primary hepatic neuroendocrine tumor: two cases report with literature review.病例报告:原发性肝神经内分泌肿瘤:两例报告并文献复习
Front Oncol. 2023 Aug 4;13:1225583. doi: 10.3389/fonc.2023.1225583. eCollection 2023.

本文引用的文献

1
A giant malignant solitary fibrous tumor in the liver: A case report.肝脏巨大恶性孤立性纤维瘤:一例报告。
Asian J Surg. 2023 Sep;46(9):3920-3923. doi: 10.1016/j.asjsur.2023.03.178. Epub 2023 Apr 28.
2
Primary Hepatic Neuroendocrine Tumor: A Case Report and Literature Review.原发性肝神经内分泌肿瘤:一例报告及文献综述
Cureus. 2022 Feb 18;14(2):e22370. doi: 10.7759/cureus.22370. eCollection 2022 Feb.
3
Neuroendocrine neoplasms of the biliary tree, liver and pancreas: a pathological approach.胆道、肝脏和胰腺神经内分泌肿瘤:一种病理方法。
Pathologica. 2021 Feb;113(1):28-38. doi: 10.32074/1591-951X-231.
4
Synergistic anti-liver cancer effects of curcumin and total ginsenosides.姜黄素与总人参皂苷协同抗肝癌作用
World J Gastrointest Oncol. 2020 Oct 15;12(10):1091-1103. doi: 10.4251/wjgo.v12.i10.1091.
5
Clinical characteristics and outcome of primary hepatic neuroendocrine tumors after comprehensive therapy.综合治疗后原发性肝脏神经内分泌肿瘤的临床特征及预后
World J Gastrointest Oncol. 2020 Sep 15;12(9):1031-1043. doi: 10.4251/wjgo.v12.i9.1031.
6
What is New in the 2019 World Health Organization (WHO) Classification of Tumors of the Digestive System: Review of Selected Updates on Neuroendocrine Neoplasms, Appendiceal Tumors, and Molecular Testing.2019 年世界卫生组织(WHO)消化系统肿瘤分类有哪些新变化:神经内分泌肿瘤、阑尾肿瘤和分子检测的部分更新介绍。
Arch Pathol Lab Med. 2021 Jun 1;145(6):664-677. doi: 10.5858/arpa.2019-0665-RA.
7
Primary hepatic neuroendocrine tumours of liver- a rarity: Single centre analysis of 13 patients.原发性肝脏神经内分泌肿瘤——一种罕见病:13例患者的单中心分析
Ann Hepatobiliary Pancreat Surg. 2020 Feb;24(1):17-23. doi: 10.14701/ahbps.2020.24.1.17. Epub 2020 Feb 27.
8
Hepatic fibrosarcoma in a middle-aged man.一名中年男性的肝纤维肉瘤。
Int J Clin Exp Pathol. 2019 Sep 1;12(9):3555-3559. eCollection 2019.
9
Focal hypersteatosis: a pseudolesion in patients with liver steatosis.局灶性脂肪变性:肝脂肪变性患者中的一种假病变。
Diagn Interv Radiol. 2019 Jan;25(1):14-20. doi: 10.5152/dir.2018.17519.
10
Current diagnostics and treatment of fibrosarcoma -perspectives for future therapeutic targets and strategies.纤维肉瘤的当前诊断与治疗——未来治疗靶点与策略的展望
Oncotarget. 2017 Aug 10;8(61):104638-104653. doi: 10.18632/oncotarget.20136. eCollection 2017 Nov 28.