McMaster M J
Princess Margaret Rose Orthopaedic Hospital, Edinburgh, Scotland.
J Bone Joint Surg Br. 1994 Sep;76(5):773-7.
Five patients with classical Ehlers-Danlos syndrome developed severe spinal deformities. Two were shown to have type-VI collagen abnormalities. Three had a double structural scoliosis of the thoracic and lumbar regions, one had a single thoracic scoliosis and one had a thoracic kyphosis. The curves first developed before the age of four years, and were not controlled by bracing. Major corrective surgery with posterior fusion was performed at a mean age of 11 years 8 months. Excessive blood loss could be controlled and although wound haematoma and dehiscence were common, they did not provide major problems. The spinal fusions healed satisfactorily.
5例患有典型埃勒斯-当洛综合征的患者出现了严重的脊柱畸形。其中2例显示有Ⅵ型胶原异常。3例有胸腰段双结构性脊柱侧凸,1例有单一胸段脊柱侧凸,1例有胸段后凸。这些脊柱侧弯最早在4岁前出现,支具治疗无效。平均在11岁8个月时进行了后路融合的主要矫正手术。术中失血过多得到了控制,虽然伤口血肿和裂开很常见,但并未造成重大问题。脊柱融合愈合情况良好。