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[儿童髋臼顶的继发性扁平]

[Secondary flattening of the acetabular roof in children].

作者信息

Mau H

机构信息

Orthopädische Universitätsklinik Tübingen.

出版信息

Z Orthop Ihre Grenzgeb. 1988 Jul-Aug;126(4):377-86. doi: 10.1055/s-2008-1044455.

Abstract

The primary "idiopathic" shallow acetabuli within the classical complex of CDH are confronted with the rare secondary "symptomatic" dysplasias of the acetabular roof. They are encountered mainly in connection with neuromuscular diseases and bad static conditions about the hip-joint. Nine cases with secondary flattening of the acetabular roof of unknown aetiology are presented, probably partially due to CDH, in connection with slight cerebral disturbances, mental and physical retardation, hypotonia of the muscles, with general constitutional laxity of joints as well as with acquired local loosening of the joint capsule due to treatment, and with insufficiency of the hip-abductors. As with the classical CDH one may observe in those cases a lateralization of the femoral head in the absence of an interposition in the joint; increasing subluxations due to joint instability with increasing shallow acetabuli may start from infancy, many years prior to puberty. If conservative treatment--not prolonged--fails and the findings are deteriorating acetabuloplasty is indicated prior to intertrochanteric adduction osteotomy during the growth-period.

摘要

先天性髋关节脱位经典综合征中的原发性“特发性”髋臼浅平,与罕见的继发性髋臼顶“症状性”发育异常相对。后者主要见于神经肌肉疾病及髋关节不良静态状况。本文报告9例病因不明的继发性髋臼顶扁平病例,可能部分与先天性髋关节脱位有关,伴有轻度脑功能障碍、智力和身体发育迟缓、肌张力低下、关节普遍松弛,以及因治疗导致的关节囊局部后天性松弛,还有髋外展肌功能不全。与经典的先天性髋关节脱位一样,在这些病例中可观察到股骨头在关节无嵌顿情况下的外移;随着髋臼变浅,关节不稳定导致的半脱位逐渐加重,可能始于婴儿期,比青春期早很多年。如果保守治疗(不延长疗程)失败且病情恶化,则在生长期行转子间内收截骨术前先行髋臼成形术。

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