Steel H H
Shriners Hospitals for Crippled Children, Philadelphia Unit, Pennsylvania 19152, USA.
J Pediatr Orthop. 1996 Nov-Dec;16(6):704-18. doi: 10.1097/00004694-199611000-00002.
Protrusio acetabuli [center-edge (C/E) angle > 60 degrees, teardrop collapsed, and pelvis invaded by acetabulum beyond ilioischial line (Köhler's)] was identified in 22 patients with classic Marfan syndrome. All had a preponderance of the syndrome's cardinal features (positive pedigree and musculoskeletal, ocular, and cardiovascular manifestations). Fifty-two immature patients with the syndrome's skeletal expressions predominating were studied for deep acetabuli. Half of these individuals (26 patients) had true protrusio acetabuli. Thirty-one percent (16 patients) had abnormal acetabular deepening (C/E angle > 50 degrees; teardrop partially collapsed without acetabular protrusion); 19% (10 patients) had normal pelves with C/E angle < 40 degrees and normal teardrop. To arrest the protrusio, the triradiate physis was closed surgically in 11 patients (21 hips), one unilaterally. In 19 operated-on hips followed-up to maturity by using teardrop, C/E angle, and acetabular relation to the ilioischial line as criteria, architecture was restored to normal in 12 hips and reduced from true protrusio to simply acetabular deepening in four. Three were unchanged. The youngest child operated on was 8; the oldest was 12 years. Laboratory examination of the physes was unrewarding.
在22例典型马凡综合征患者中发现髋臼前突(中心边缘(C/E)角>60度,泪滴塌陷,髋臼侵犯骨盆超过髂耻线(科勒氏线))。所有患者均具有该综合征的主要特征(阳性家族史以及肌肉骨骼、眼部和心血管表现)。对52例以该综合征骨骼表现为主的未成熟患者进行了深髋臼研究。其中一半(26例患者)有真正的髋臼前突。31%(16例患者)有髋臼异常加深(C/E角>50度;泪滴部分塌陷但无髋臼前突);19%(10例患者)骨盆正常,C/E角<40度且泪滴正常。为阻止前突,对11例患者(21髋)进行了手术闭合三叉骨骺,其中1例为单侧。在19例接受手术的髋部中,以泪滴、C/E角以及髋臼与髂耻线的关系为标准随访至成熟,12髋的结构恢复正常,4髋从真正的髋臼前突减轻为单纯的髋臼加深。3髋无变化。接受手术的最年幼患儿为8岁;最年长患儿为12岁。对骨骺进行实验室检查未取得有价值的结果。