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戈勒姆-斯托特病和全身性淋巴管异常的颅面CT表现。

Craniofacial CT findings of Gorham-Stout disease and generalized lymphatic anomaly.

作者信息

Kato Hiroki, Ozeki Michio, Fukao Toshiyuki, Matsuo Masayuki

机构信息

Department of Radiology, Gifu University School of Medicine, 1-1 Yanagido, Gifu, 501-1194, Japan.

Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan.

出版信息

Neuroradiology. 2016 Aug;58(8):801-6. doi: 10.1007/s00234-016-1691-0. Epub 2016 Apr 28.

DOI:10.1007/s00234-016-1691-0
PMID:27126342
Abstract

INTRODUCTION

The present study aimed to assess the craniofacial CT imaging features for differentiating between Gorham-Stout disease (GSD) and generalized lymphatic anomaly (GLA).

METHODS

Seven patients with GSD and four patients with GLA were included in this study. All patients underwent CT examinations that encompassed the craniofacial bones. The presence, distribution, and type of craniofacial osteolysis were assessed. The clinical symptoms that were associated with craniofacial osteolysis were also reviewed.

RESULTS

Craniofacial osteolysis including cranial osteolysis was seen in four of seven (57 %) patients with GSD and in three of four (75 %) patients with GLA. Facial osteolysis was seen in two (29 %) patients with GSD, but this was not observed in patients with GLA. Among patients with craniofacial osteolysis, those with GSD showed diffuse involvement, whereas those with GLA showed multifocal involvement. The craniofacial osteolysis of GSD could be classified into three patterns: medullary involvement, thinning bone, and disappearing bone. The clinical symptoms of craniofacial osteolysis were observed in all patients with GSD but were not present in patients with GLA.

CONCLUSION

Craniofacial involvement was observed in both groups. The craniofacial osteolysis of GSD showed diffuse involvement with clinical symptoms, whereas that of GLA showed multifocal involvement without clinical symptoms.

摘要

引言

本研究旨在评估颅面部CT成像特征,以鉴别戈勒姆-斯托特病(GSD)和泛发性淋巴管畸形(GLA)。

方法

本研究纳入了7例GSD患者和4例GLA患者。所有患者均接受了包括颅面部骨骼的CT检查。评估颅面部骨质溶解的存在、分布和类型。还回顾了与颅面部骨质溶解相关的临床症状。

结果

7例GSD患者中有4例(57%)出现包括颅骨骨质溶解在内的颅面部骨质溶解,4例GLA患者中有3例(75%)出现。2例(29%)GSD患者出现面部骨质溶解,但GLA患者未观察到。在颅面部骨质溶解患者中,GSD患者表现为弥漫性受累,而GLA患者表现为多灶性受累。GSD的颅面部骨质溶解可分为三种类型:骨髓受累、骨质变薄和骨质消失。所有GSD患者均观察到颅面部骨质溶解的临床症状,而GLA患者未出现。

结论

两组均观察到颅面部受累。GSD的颅面部骨质溶解表现为伴有临床症状的弥漫性受累,而GLA的颅面部骨质溶解表现为无临床症状的多灶性受累。

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2
Personalized Therapy for Generalized Lymphatic Anomaly/Gorham-Stout Disease With a Combination of Sunitinib and Taxol.舒尼替尼与紫杉醇联合用于广泛性淋巴管瘤病/戈勒姆-斯托特病的个体化治疗
J Pediatr Hematol Oncol. 2015 Nov;37(8):e481-5. doi: 10.1097/MPH.0000000000000436.
3
Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies.
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Pediatrics. 2015 Jul;136(1):e203-14. doi: 10.1542/peds.2014-3673. Epub 2015 Jun 8.
4
Simple lymphangioma to generalized lymphatic anomaly: role of imaging in disclosure of a rare and morbid disease.单纯性淋巴管瘤至广泛性淋巴管异常:影像学在罕见且严重疾病诊断中的作用
Case Rep Radiol. 2015;2015:603859. doi: 10.1155/2015/603859. Epub 2015 Apr 12.
5
Gorham-Stout disease: radiological, histological, and clinical features of 12 cases and review of literature.戈勒姆-斯托特病:12例患者的放射学、组织学及临床特征并文献复习
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6
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