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Maffucci lymphangioma syndrome: an unusual variant of Ollier's disease, a case report and a review of the literature.

作者信息

Auyeung Jeff, Mohanty Khitish, Tayton Keith

机构信息

Department of Orthopaedics, Royal Gwent Hospital, Newport, South Wales, UK.

出版信息

J Pediatr Orthop B. 2003 Mar;12(2):147-50. doi: 10.1097/01.bpb.0000049563.52224.ef.

DOI:10.1097/01.bpb.0000049563.52224.ef
PMID:12584501
Abstract

A case of Maffucci's syndrome in an 18-month old boy is presented, in which the vascular malformation consists of lymphangioma. This is a rare variant of Maffucci's syndrome. So far only six other cases have been reported in which lymphangiomas featured. We believe that the case described here is only the second case to be reported for which a lymphangioma is the only vascular malformation in the syndrome. The literature of the other six cases was reviewed and various features identified enabling this particular disease to be classified as a distinct variant of Maffucci's syndrome.

摘要

相似文献

1
Maffucci lymphangioma syndrome: an unusual variant of Ollier's disease, a case report and a review of the literature.
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2
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引用本文的文献

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World J Surg Oncol. 2022 Jun 29;20(1):218. doi: 10.1186/s12957-022-02686-z.
2
Juvenile granulosa cell tumor associated with Ollier disease.与骨软骨瘤病相关的青少年颗粒细胞瘤。
Indian J Med Paediatr Oncol. 2016 Oct-Dec;37(4):293-295. doi: 10.4103/0971-5851.195749.
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Somatic IDH1 mutation in a pituitary adenoma of a patient with Maffucci syndrome.
马富西综合征患者垂体腺瘤中的体细胞异柠檬酸脱氢酶1(IDH1)突变
J Neurosurg. 2016 Jun;124(6):1562-7. doi: 10.3171/2015.4.JNS15191. Epub 2015 Oct 16.
4
Common somatic alterations identified in maffucci syndrome by molecular karyotyping.通过分子核型分析在马富西综合征中鉴定出的常见体细胞改变。
Mol Syndromol. 2014 Dec;5(6):259-67. doi: 10.1159/000365898. Epub 2014 Aug 26.
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Bone scintigraphy in Ollier's disease: A rare case report.骨软骨瘤病的骨闪烁显像:1例罕见病例报告。
Indian J Nucl Med. 2013 Oct;28(4):226-9. doi: 10.4103/0972-3919.121968.
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Enchondromatosis: insights on the different subtypes.内生软骨瘤病:不同亚型的见解
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