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戈谢病:消失的骨头。

Gorham's disease: the disappearing bone.

机构信息

Department of Nuclear Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.

出版信息

Clin Nucl Med. 2013 May;38(5):361-4. doi: 10.1097/RLU.0b013e318286bf93.

DOI:10.1097/RLU.0b013e318286bf93
PMID:23486335
Abstract

Gorham's disease is a rare disorder characterized by proliferation of vascular channels. The clinical presentation of Gorham's disease is variable and depends on the site of involvement. A high index of clinical suspicion is needed for accurate diagnosis, and recognition of distinctive radiologic and histopathologic features can help facilitate and expedite diagnosis. The subsequent images were obtained from a 31-year-old male patient. Nuclear scintigraphy and computed tomography identified active bone destruction in the lower thoracic and upper lumbar spine in addition to the absence of the left lower rib cage. Gorham's disease was subsequently confirmed by biopsy.

摘要

戈谢病是一种罕见的疾病,其特征是血管通道的增殖。戈谢病的临床表现多种多样,取决于受累部位。准确诊断需要高度的临床怀疑指数,识别独特的放射学和组织病理学特征有助于促进和加快诊断。以下是一名 31 岁男性患者的后续图像。核闪烁扫描和计算机断层扫描除了左胸下肋骨缺失外,还确定了下胸椎和上腰椎的活动性骨破坏。随后的活检证实了戈谢病的诊断。

相似文献

1
Gorham's disease: the disappearing bone.戈谢病:消失的骨头。
Clin Nucl Med. 2013 May;38(5):361-4. doi: 10.1097/RLU.0b013e318286bf93.
2
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MRI of Gorham's disease: findings in two cases.戈谢病的磁共振成像:两例病例的影像学表现
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Gorham's disease of the mandible: radiological features.下颌骨戈勒姆病:影像学特征。
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Mediastinal lymphangioma and chylothorax: thoracic involvement of Gorham's disease.纵隔淋巴管瘤与乳糜胸:戈勒姆病的胸部累及情况
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引用本文的文献

1
Clinical features and current management experience in Gorham-Stout disease: a systematic review.戈勒姆-斯托特病的临床特征与当前治疗经验:一项系统评价
Orphanet J Rare Dis. 2025 Mar 19;20(1):134. doi: 10.1186/s13023-025-03649-9.
2
Treatment of gorham-stout disease with bisphosphonates and total hip arthroplasty: A case report.双膦酸盐和全髋关节置换术治疗戈谢病:一例报告。
Front Surg. 2023 Jan 30;10:1078869. doi: 10.3389/fsurg.2023.1078869. eCollection 2023.
3
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.