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病例报告631:多腺体自身免疫(施密特)综合征中的新骨疏松症(干骺端骨质减少)

Case report 631: Neo-osseous porosis (metaphyseal osteopenia) in polyglandular autoimmune (Schmidt) syndrome.

作者信息

Vela B S, Dorin R I, Hartshorne M F

机构信息

Department of Medicine, Albuquerque Veterans Administration Medical Center, NM 87108.

出版信息

Skeletal Radiol. 1990;19(6):468-71. doi: 10.1007/BF00241809.

Abstract

In summary, a case is reported of a patient with the radiographic findings of diffuse, symmetrical metaphyseal osteopenia of long bones. A constellation termed neo-osseous porosis, associated with polyendocrine failure (Schmidt syndrome) involving the thyroid gland, adrenal glands, and gonads has been described in this case. Neo-osseous porosis has been observed previously in idiopathic juvenile osteoporosis. This case represents the first instance in which this distinctive radiographic picture has been observed in the setting of specific (multiple) endocrine dysfunction disorders.

摘要

总之,本文报告了一例患者,其长骨的X线表现为弥漫性、对称性干骺端骨质减少。该病例中描述了一种称为新骨疏松症的症候群,它与涉及甲状腺、肾上腺和性腺的多内分泌腺功能减退(施密特综合征)相关。新骨疏松症先前已在特发性青少年骨质疏松症中观察到。该病例是首次在特定(多种)内分泌功能障碍性疾病背景下观察到这种独特的X线表现。

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