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Conservative surgical management of simple monostotic fibrous dysplasia of the proximal femur in a 19-year-old basketballer: a case report

机译:19岁篮球运动员近端股骨简单单晶纤维发育不良的保守手术管理:案例报告

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摘要

Abstract Background Fibrous dysplasia is a rare benign, intramedullary, fibro-osseous lesion. It is thought to be a developmental disorder of bone maturation where normal lamellar bone is replaced by irregular trabecular bone ensnared with fibrous dysplastic tissue that is unable to complete maturation resulting in significant loss of mechanical strength. This, together with the inability to mineralize sufficiently, leads to deformity, pain, and pathological fractures. It typically presents in young adults, with an equal representation in both genders. Surgical intervention is necessary in mild cases with chronic symptoms to prevent pathological fractures or to correct deformities. Case presentation A 19-year-old Chinese woman presented with non-traumatic, nonspecific left hip pain during basketball training. X-rays demonstrated a ground glass lesion, 10 cm in length, in her left femoral neck, which is a classic sign of fibrous dysplasia. No other deformities were noted. She was managed conservatively with analgesia for 6 months; however, her condition did not improve and a decision was made for surgical intervention. The lesion was a type 1 lesion according to the Ippolito radiological classification of fibrous dysplasia, which is a lesion with mild deformities. Therefore, we performed minimal curettage and insertion of a free autologous fibula strut harvested from her left leg, for structural stability. No implants were used. The operation was successful and her postoperative course was uneventful. Histology confirmed the diagnosis of fibrous dysplasia. She achieved partial weight bearing at 4 weeks postoperation, and full weight bearing at 8 weeks, and returned to basketball at 12 weeks. At 1-year follow-up, she returned to competitive basketball and remained pain free with no complications. Conclusions Fibrous dysplasia is a rare and benign fibrous tumor of the bone that presents mostly in a young patient population. From our case, we have shown that it is possible to treat young patients with uncomplicated Ippolito type 1 fibrous dysplasia with a minimally invasive approach of using a cortical bone graft for structural augmentation of the affected area, without the use of implants. They are able to fully return to an active and vigorous lifestyle without restriction of activities or long-term risks of orthopedic implant complications.
机译:摘要背景纤维发育不良是一种罕见的良性,髓内,纤维 - 骨质病变。据认为是骨骼成熟的发育障碍,其中正常的层状骨被不规则的小梁骨钝腹肌,其纤维发育血管组织不能完成成熟,导致机械强度显着损失。这与能够充分地融化,导致畸形,疼痛和病理骨折。它通常在年轻的成年人中呈现出在两个人中具有相同的代表性。在慢性症状的轻度案件中是必需的手术干预,以防止病理骨折或纠正畸形。案例介绍一位19岁的中国女性在篮球训练期间呈现非创伤,非特异性左髋关节疼痛。 X射线在她的左股骨颈中展示了磨砂玻璃病变,10厘米,是纤维发育不良的经典迹象。没有注意到其他畸形。她保守治疗镇痛6个月;然而,她的病情并没有改善,并对手术干预进行决定。根据纤维性发育不良的IPPolito放射性分类,病变是1型病变,这是一种具有温和畸形的病变。因此,我们进行了最小的刮痕和从左腿收获的自由自体腓骨支柱,用于结构稳定性。没有使用植入物。该行动成功,她的术后课程是不行的。组织学证实了纤维发育不良的诊断。她在术后4周达到部分重量,并在8周内全重轴承,并在12周返回篮球。在1年的随访时间里,她回到了竞争力的篮球,没有任何并发​​症仍然无痛苦。结论纤维发育不良是骨骼的罕见和良性纤维肿瘤,主要是年轻患者人口。从我们的情况来看,我们已经表明,可以治疗患有简单的IPPolito型1型纤维性发育不良的年轻患者,其使用皮质骨移植物的微创方法来使用植入物的结构增强。他们能够完全恢复积极和充满活力的生活方式,而不限制骨科植入复杂性的活动或长期风险。

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