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Spinal deformity in patients born with oesophageal atresia and tracheo-oesophageal fistula.

机译:食管闭锁合并气管食管瘘患者的脊柱畸形。

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摘要

Spinal deformity was present in 58 (19%) of 302 patients born with oesophageal atresia and fistula when examined at review. This was present in 24 (47%) of 51 patients with vertebral anomalies and 34 (14%) of 251 patients with normal vertebrae. Scoliosis was present in 21 patients with vertebral anomalies, torticollis in two, and lordosis in one. Two thirds of the patients with congenital scoliosis have had or are likely to require operation, compared with five patients with non-congenital scoliosis. Scoliosis associated with mixed vertebral anomalies in the lower thoracic spine had the worst prognosis. The medical records of a further 64 patients who had survived operation but who could not be traced were reviewed, and indicated that four had had congenital vertebral anomalies but none had a spinal deformity. We recommend early detection of vertebral anomalies in this group and careful follow up of patients with these abnormalities.
机译:回顾检查时,在302例食管闭锁和瘘管出生的患者中,脊柱畸形存在于58名(19%)。 51例椎骨异常患者中有24例(47%),而251例椎骨正常患者中有34例(14%)。脊柱侧弯存在于21例椎骨异常患者中,斜颈为2例,脊柱前凸为1例。与五名非先天性脊柱侧弯患者相比,三分之二的先天性脊柱侧弯患者已经或可能需要手术。下胸椎混合脊椎异常合并脊柱侧弯的预后最差。回顾了另外64例手术后幸存但无法追踪的患者的病历,并指出有4例患有先天性椎体异常,但无脊柱畸形。我们建议在这一组中尽早发现椎骨异常,并对这些异常的患者进行仔细的随访。

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