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进行性骨干发育不良:病例报告及文献综述

Progressive diaphyseal dysplasia: case report and literature review.

作者信息

Aggarwal P, Wali J P, Sharma S K

机构信息

Department of Medicine, All-India Institute of Medical Sciences, New Delhi.

出版信息

Orthopedics. 1990 Aug;13(8):901-4. doi: 10.3928/0147-7447-19900801-14.

DOI:10.3928/0147-7447-19900801-14
PMID:2204043
Abstract

We describe a case of progressive diaphyseal dysplasia occurring sporadically in a 25-year-old woman. This patient had menorrhagia, and severe anemia and hepatosplenomegaly, unusual clinical features of this disease.

摘要

我们描述了一例25岁女性散发性发生的进行性骨干发育异常病例。该患者有月经过多、严重贫血和肝脾肿大,这些都是该疾病不常见的临床特征。

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1
Progressive diaphyseal dysplasia: case report and literature review.进行性骨干发育不良:病例报告及文献综述
Orthopedics. 1990 Aug;13(8):901-4. doi: 10.3928/0147-7447-19900801-14.
2
High-dose intravenous methylprednisolone therapy for anemia associated with diaphyseal dysplasia.
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Diaphyseal dysplasia associated with anemia.
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A Rare Sporadic Case of Camurati-Engelmann Disease With Jaw Involvement.一例罕见的累及颌骨的散发性卡穆拉蒂-恩格尔曼病病例。
J Oral Maxillofac Surg. 2017 Nov;75(11):2385-2390. doi: 10.1016/j.joms.2017.03.059. Epub 2017 Apr 14.
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[An incidental finding of a progressive diaphyseal dysplasia (Camurati-Engelmann syndrome)].
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[Camurati-Engelmann disease (progressive diaphyseal dysplasia). Differential diagnostic problems].[卡姆拉蒂-恩格尔曼病(进行性骨干发育不良)。鉴别诊断问题]
Unfallchirurgie. 1989 Apr;15(2):104-7.
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Metaphyseal dysplasia, epiphyseal dysplasia, diaphyseal dysplasia, and related conditions. III. Progressive diaphyseal dysplasia.干骺端发育异常、骨骺发育异常、骨干发育异常及相关病症。III. 进行性骨干发育异常
AMA Arch Intern Med. 1954 Dec;94(6):902-10. doi: 10.1001/archinte.1954.00250060036003.
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[Diaphyseal dysplasia (Camurati-Engelmann syndrome) with progressive loss of vision: 30-year observations and the effect of prednisolone treatment (author's transl)].
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[Otolaryngological aspects of Camurati-Engelmann disease (progressive diaphyseal dysplasia): review of literature and report of one case].
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Ghosal type hemato-diaphyseal dysplasia: a rare variety of Engelmann's disease.
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