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骨质溶解症(戈勒姆-斯托特病):一例随访48年的病例报告。

Disappearing bone disease (Gorham-stout disease): report of a case with a follow-up of 48 years.

作者信息

Rauh G, Gross M

机构信息

Medizinische Poliklinik, Klinikum Innenstadt der Ludwig-Maximilians-Universität Pettenkoferstr. 8a Munich D-80336 Germany +49 89/5160 3511 +49 89/5160 4439.

出版信息

Eur J Med Res. 1997 Oct 30;2(10):425-7.

PMID:9348269
Abstract

A patient with osteolysis of the right hand after a metatarsal fracture at the age of 12 years is reported. The osteolysis progressed until the age of 21 years and was stable until the age of 59 years, when the patient died from a metastatic colon cancer. The article discusses the clinical, radiographic, and histologic features, and prognosis of idiopathic osteolysis (Gorham-Stout disease). Gorham-Stout disease is characterized by a non-familial, histological benign vascular proliferation producing lysis of the bone. The therapeutic options of Gorham-Stout disease is limited; radiotherapy has been used with success in single cases. Usually, the disease undergoes spontaneous arrest, as it occurred in our patient.

摘要

本文报告了一名12岁时跖骨骨折后右手出现骨质溶解的患者。骨质溶解一直进展到21岁,之后保持稳定,直到59岁患者死于转移性结肠癌。本文讨论了特发性骨质溶解(戈勒姆-斯托特病)的临床、影像学和组织学特征以及预后。戈勒姆-斯托特病的特点是一种非家族性的、组织学上良性的血管增生导致骨质溶解。戈勒姆-斯托特病的治疗选择有限;放射治疗在个别病例中取得了成功。通常,该病会自行停止发展,就像我们的患者那样。

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1
Disappearing bone disease (Gorham-stout disease): report of a case with a follow-up of 48 years.骨质溶解症(戈勒姆-斯托特病):一例随访48年的病例报告。
Eur J Med Res. 1997 Oct 30;2(10):425-7.
2
[Gorham-Stout disease: report of a case affecting the right hand with a follow-up of 24 years].
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引用本文的文献

1
Gorham-Stout Disease with Multiple Bone Involvement-Challenging Diagnosis of a Rare Disease and Literature Review.戈勒姆-斯托特病伴多发骨累及——罕见病的诊断挑战及文献复习。
Medicina (Kaunas). 2021 Jul 2;57(7):681. doi: 10.3390/medicina57070681.
2
Gorham-Stout disease: good results of bisphosphonate treatment in 6 of 7 patients.戈勒姆-斯托特病:7 例患者中有 6 例双磷酸盐治疗效果良好。
Acta Orthop. 2020 Apr;91(2):209-214. doi: 10.1080/17453674.2019.1709716. Epub 2020 Jan 13.
3
Complex single step skull reconstruction in Gorham's disease - a technical report and review of the literature.
戈谢病复杂单步颅骨重建——技术报告及文献综述
BMC Surg. 2015 Mar 11;15:24. doi: 10.1186/s12893-015-0014-4.
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Reossification in Gorham's disease of the hand and wrist with unusual CT and MR imaging features.手部和腕部戈谢病的再骨化,具有不寻常的CT和MR成像特征。
Skeletal Radiol. 2015 Jul;44(7):1033-8. doi: 10.1007/s00256-015-2121-9. Epub 2015 Feb 26.
5
A Rare Case of Gorham's Disease: Primary Ulnar Involvement with Secondary Spread to the Radius and Elbow.骨肥大性骨关节病罕见病例:原发性尺骨受累并继发累及桡骨和肘部
Trauma Mon. 2013 Spring;18(1):41-5. doi: 10.5812/traumamon.9905. Epub 2013 May 26.
6
Gorham-Stout syndrome in mainland China: a case series of 67 patients and review of the literature.中国大陆戈谢病综合征:67 例患者的病例系列及文献复习。
J Zhejiang Univ Sci B. 2013 Aug;14(8):729-35. doi: 10.1631/jzus.B1200308.
7
Gorham-Stout disease: the experience of the Rizzoli Institute and review of the literature.戈勒姆-斯托特病:里佐利研究所的经验及文献回顾。
Skeletal Radiol. 2011 Nov;40(11):1391-7. doi: 10.1007/s00256-010-1051-9. Epub 2010 Oct 25.
8
Absent right iliac bone on Tc99m MDP bone scan in a patient with Gorham's vanishing bone disease.戈谢病性骨质溶解症患者的锝99m亚甲基二膦酸盐骨扫描显示右侧髂骨缺失。
Indian J Nucl Med. 2010 Jan;25(1):23-4. doi: 10.4103/0972-3919.63596.
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Gorham's disease or massive osteolysis.戈谢病或大块骨质溶解症。
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Massive Gorham-Stout syndrome of the pelvis.骨盆巨大型戈勒姆-斯托特综合征
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