• 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

活体亲属肝移植供体候选者中的肝紫癜病

Peliosis hepatis in a living related liver transplantation donor candidate.

作者信息

Testa Giuliano, Panaro Fabrizio, Sankary Howard, Chejfec Gregorio, Mohanty Smruti, Benedetti Enrico, Layden Thomas

机构信息

University of Illinois at Chicago, Chicago, IL, USA.

出版信息

J Gastroenterol Hepatol. 2006 Jun;21(6):1075-7. doi: 10.1111/j.1440-1746.2006.03172.x.

DOI:10.1111/j.1440-1746.2006.03172.x
PMID:16725002
Abstract

Peliosis hepatis is a rare benign condition histologically characterized by multiple cystic blood-filled spaces distributed throughout the liver parenchyma. Peliosis hepatis has been associated with malignancies, immunosuppression, infections and medications. We report a case of peliosis hepatis in a candidate for living liver donation, which regressed with restitutio ad integrum, after the noxious stimulus was stopped. We conclude that after diagnosis of peliosis hepatis is established and its cause is removed, simple radiographic imaging is sufficient to document the restitutio ad integrum of the parenchyma, avoiding repeat histological confirmation.

摘要

肝紫癜是一种罕见的良性疾病,组织学特征为多个充满血液的囊性间隙分布于整个肝实质。肝紫癜与恶性肿瘤、免疫抑制、感染及药物有关。我们报告一例活体肝供体候选者发生肝紫癜的病例,在停止有害刺激后,肝紫癜完全恢复。我们得出结论,在确诊肝紫癜并去除其病因后,简单的影像学检查足以记录肝实质的完全恢复,无需重复组织学确认。

相似文献

1
Peliosis hepatis in a living related liver transplantation donor candidate.活体亲属肝移植供体候选者中的肝紫癜病
J Gastroenterol Hepatol. 2006 Jun;21(6):1075-7. doi: 10.1111/j.1440-1746.2006.03172.x.
2
Idiopathic extensive peliosis hepatis treated with liver transplantation.肝移植治疗特发性广泛性肝紫癜病。
J Hepatobiliary Pancreat Surg. 2004;11(5):371-4. doi: 10.1007/s00534-004-0908-5.
3
Lipiodol accumulation in focal peliosis hepatis with sinusoidal dilatation.脂碘油在伴有窦性扩张的局灶性肝紫癜中的蓄积。
J Clin Gastroenterol. 2001 Apr;32(4):356-8. doi: 10.1097/00004836-200104000-00018.
4
Contrast enhanced ultrasound of a rare case of Peliosis hepatis.肝紫癜罕见病例的超声造影检查
Med Ultrason. 2017 Jan 31;19(1):114-116. doi: 10.11152/mu-940.
5
[Peliosis hepatis. A clinical status inventory].[肝紫癜病。临床状况清单]
Z Gastroenterol. 1982 Dec;20(12):710-21.
6
Peliosis hepatis and systemic lupus erythematosus: A rare condition identified by magnetic resonance imaging.肝紫癜病与系统性红斑狼疮:一种通过磁共振成像识别出的罕见病症。
Rev Assoc Med Bras (1992). 2018 Jan;64(1):19-21. doi: 10.1590/1806-9282.64.01.19.
7
Case report: radiological appearances in peliosis hepatis.病例报告:肝紫癜病的影像学表现
Br J Radiol. 1994 Jan;67(793):102-4. doi: 10.1259/0007-1285-67-793-102.
8
Peliosis Hepatis in a Child with X-Linked Myotubular Myopathy Treated with Living-Donor Liver Transplant: A Case Report.X 连锁肌小管肌病患儿行活体肝移植术后肝小泡变性:病例报告
Transplant Proc. 2021 May;53(4):1317-1321. doi: 10.1016/j.transproceed.2020.10.033. Epub 2021 Jan 16.
9
An autopsy case of peliosis hepatis with X-linked myotubular myopathy.1例伴有X连锁肌管性肌病的肝紫癜尸检病例。
Leg Med (Tokyo). 2019 May;38:77-82. doi: 10.1016/j.legalmed.2019.04.005. Epub 2019 Apr 18.
10
Peliosis hepatis with pseudotumoral and hemorrhagic evolution: CT and MR findings.伴有假瘤样和出血性演变的肝紫癜:CT和MR表现
Abdom Imaging. 2001 Mar-Apr;26(2):197-9. doi: 10.1007/s002610000131.

引用本文的文献

1
Peliosis hepatis: 2 case reports of a rare liver disorder and its differential diagnosis.肝紫癜病:罕见肝脏疾病的2例报告及其鉴别诊断
Medicine (Baltimore). 2017 Mar;96(13):e6471. doi: 10.1097/MD.0000000000006471.
2
Peliosis hepatis presenting with massive hepatomegaly in a patient with idiopathic thrombocytopenic purpura.一名特发性血小板减少性紫癜患者出现肝紫癜并伴有巨肝。
Clin Mol Hepatol. 2015 Dec;21(4):387-92. doi: 10.3350/cmh.2015.21.4.387. Epub 2015 Dec 24.
3
Peliosis hepatis complicated by portal hypertension following renal transplantation.
肾移植后肝紫癜合并门静脉高压
World J Gastroenterol. 2014 Mar 7;20(9):2420-5. doi: 10.3748/wjg.v20.i9.2420.
4
Pituitary adenoma with peliosis: a report of two cases.垂体腺瘤伴紫癜:两例报告。
Endocr Pathol. 2009 Spring;20(1):41-5. doi: 10.1007/s12022-008-9056-9.