• 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

戈勒姆-斯托特病:来自叙利亚的一例病例报告。

Gorham Stout disease: a case report from Syria.

作者信息

Esper Asil, Alhoulaiby Sami, Emran Areege, Youssef Safwan, Alshehabi Zuheir

机构信息

Neurology Department, Tishreen University Hospital, Halap street, Latakia, Syria.

Faculty of Medicine, Damascus University, Damascus, Syria.

出版信息

Oxf Med Case Reports. 2021 Jan 12;2021(1):omaa121. doi: 10.1093/omcr/omaa121. eCollection 2021 Jan.

DOI:10.1093/omcr/omaa121
PMID:33469472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7802812/
Abstract

Gorham-Stout disease (GSD) is a rare entity that destroys the bone matrix resulting mainly in osteolysis, pain and pathologic fractures among a broader clinical picture. We report a case of a 60-year-old female with a sudden discovery of pathologic fractures in the pelvis and the absence of the left femoral head. On biopsy, no cellular atypia was found, instead disturbed bone formation with prominent vascularity with scattered foci of necrosis & osteolysis, which lead to the diagnosis of GSD. Possible differential diagnoses were discussed and excluded. The patient was put on Bisphosphonate that led to a relative improvement in the symptoms. This disease needs a more thorough investigation to identify the key cause, what is beyond the scope of this report.

摘要

戈勒姆-斯托特病(GSD)是一种罕见的疾病,它破坏骨基质,在更广泛的临床症状中主要导致骨质溶解、疼痛和病理性骨折。我们报告一例60岁女性病例,该患者突然发现骨盆病理性骨折且左股骨头缺失。活检时未发现细胞异型性,而是骨形成紊乱,血管明显,伴有散在的坏死灶和骨质溶解,这导致了戈勒姆-斯托特病的诊断。讨论并排除了可能的鉴别诊断。患者接受了双膦酸盐治疗,症状有相对改善。这种疾病需要更深入的研究以确定关键病因,这超出了本报告的范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/590b66d51498/omaa121f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/2c892d2f8092/omaa121f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/add6fda8a16a/omaa121f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/60135376a9bc/omaa121f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/fca0b4484654/omaa121f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/590b66d51498/omaa121f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/2c892d2f8092/omaa121f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/add6fda8a16a/omaa121f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/60135376a9bc/omaa121f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/fca0b4484654/omaa121f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f784/7802812/590b66d51498/omaa121f5.jpg

相似文献

1
Gorham Stout disease: a case report from Syria.戈勒姆-斯托特病:来自叙利亚的一例病例报告。
Oxf Med Case Reports. 2021 Jan 12;2021(1):omaa121. doi: 10.1093/omcr/omaa121. eCollection 2021 Jan.
2
From tooth extraction to Gorham-Stout disease: A case report.从拔牙到戈勒姆-斯托特病:一例报告。
Int J Surg Case Rep. 2017;34:110-114. doi: 10.1016/j.ijscr.2017.03.028. Epub 2017 Mar 21.
3
Viewpoints on vessels and vanishing bones in Gorham-Stout disease.关于戈勒姆-斯托特病中血管与骨质消失的观点。
Bone. 2014 Jun;63:47-52. doi: 10.1016/j.bone.2014.02.011. Epub 2014 Feb 26.
4
A case of restitution ad integrum in Gorham-Stout disease.一例 Gorham-Stout 病的整体复位。
Joint Bone Spine. 2023 Jan;90(1):105478. doi: 10.1016/j.jbspin.2022.105478. Epub 2022 Nov 1.
5
Gorham-Stout disease of the malleolus: a rare case report.距骨-斯塔特病:1 例罕见病例报告。
BMC Musculoskelet Disord. 2019 Dec 31;21(1):3. doi: 10.1186/s12891-019-3027-9.
6
Combined neodymium-doped yttrium aluminum garnet laser and sclerotherapy in Gorham-Stout syndrome.钕掺杂钇铝石榴石激光与硬化疗法联合治疗戈勒姆-斯托特综合征
JAAD Case Rep. 2018 Apr 30;4(5):458-461. doi: 10.1016/j.jdcr.2018.01.017. eCollection 2018 Jun.
7
Gorham-Stout disease successfully treated with sirolimus (rapamycin): a case report and review of the literature.西罗莫司(雷帕霉素)成功治疗戈谢病 - 斯托特病:一例报告并文献复习
BMC Musculoskelet Disord. 2020 Aug 25;21(1):577. doi: 10.1186/s12891-020-03540-7.
8
Gorham-Stout Disease: A Case Report and Review of the Literature.戈勒姆-斯托特病:一例报告及文献综述
Cureus. 2023 May 9;15(5):e38756. doi: 10.7759/cureus.38756. eCollection 2023 May.
9
A Large Skull Defect Due to Gorham-Stout Disease: Case Report and Literature Review on Pathogenesis, Diagnosis, and Treatment.一例由戈谢病导致的巨大颅骨缺损:病例报告及关于发病机制、诊断和治疗的文献综述
Front Endocrinol (Lausanne). 2020 Feb 5;11:37. doi: 10.3389/fendo.2020.00037. eCollection 2020.
10
Two cases of Gorham-Stout disease with good response to zoledronic acid treatment.两例戈谢病(Gorham-Stout disease)患者对唑来膦酸治疗反应良好。
Clin Cases Miner Bone Metab. 2017 May-Aug;14(2):250-253. doi: 10.11138/ccmbm/2017.14.2.250. Epub 2017 Oct 25.

引用本文的文献

1
Vanishing the Existence of the Mandible?下颌骨消失了?
Contemp Clin Dent. 2023 Apr-Jun;14(2):176-178. doi: 10.4103/ccd.ccd_545_22. Epub 2023 Jun 30.
2
The molecular mechanism of Gorham syndrome: an update.戈勒姆综合征的分子机制:更新。
Front Immunol. 2023 May 5;14:1165091. doi: 10.3389/fimmu.2023.1165091. eCollection 2023.
3
Vanishing Bone Disease of the Thoracic Cage: Challenges in the Management of a Rare Entity.胸廓消失性骨病:罕见病管理中的挑战

本文引用的文献

1
Generalized Lymphatic Anomaly and Gorham-Stout Disease: Overview and Recent Insights.全身性淋巴管异常与戈勒姆-斯托特病:概述与最新见解
Adv Wound Care (New Rochelle). 2019 Jun 1;8(6):230-245. doi: 10.1089/wound.2018.0850. Epub 2019 Jun 6.
2
Gorham's disease of mandible--a rare case presentation in pediatric patient.下颌骨戈谢病——一例儿科患者的罕见病例报告
J Indian Soc Pedod Prev Dent. 2016 Apr-Jun;34(2):180-4. doi: 10.4103/0970-4388.180450.
3
Vanishing bone disease (Gorham-Stout syndrome): A review of a rare entity.骨质消失症(戈勒姆-斯托特综合征):一种罕见病症的综述
AACE Clin Case Rep. 2021 Sep 20;8(2):65-68. doi: 10.1016/j.aace.2021.09.002. eCollection 2022 Mar-Apr.
World J Orthop. 2014 Nov 18;5(5):694-8. doi: 10.5312/wjo.v5.i5.694.
4
Viewpoints on vessels and vanishing bones in Gorham-Stout disease.关于戈勒姆-斯托特病中血管与骨质消失的观点。
Bone. 2014 Jun;63:47-52. doi: 10.1016/j.bone.2014.02.011. Epub 2014 Feb 26.
5
Vanishing bone disease: a review.骨质消失症:综述
J Oral Maxillofac Surg. 2011 Jan;69(1):199-203. doi: 10.1016/j.joms.2010.05.088. Epub 2010 Oct 27.
6
Vanishing bone disease involving the pelvis.累及骨盆的骨质消失性疾病。
J Cancer Res Ther. 2005 Oct-Dec;1(4):227-8. doi: 10.4103/0973-1482.19592.
7
Perspectives on massive osteolysis. Report of a case and review of the literature.关于大量骨质溶解的观点。病例报告及文献综述。
Oral Surg Oral Med Oral Pathol. 1983 Apr;55(4):331-43. doi: 10.1016/0030-4220(83)90185-8.