Total Knee Replacement for Varus Deformity in Osteoarthritis of Knee with Multiple Hereditary Exostoses - A Rare Case Report.

Chaitanya Vyawahare, Rohan Bhargava, Shivaram Muthiah, U N Rakesh, Peeyush Belsare
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Abstract

Introduction: Multiple hereditary exostosis (MHE) is a genetic condition inherited in an autosomal dominant manner, resulting from point mutations in exostosin genes. Knee deformities, such as genu valgus, are common in individuals with MHE, often localized to the proximal tibial metaphysis, and occasionally involving the femur. Osteochondromas at the knee can lead to an oblique joint line orientation, contributing to earlier onset arthritis. Increased angulation may also lead to lateral patella subluxation and patellofemoral complaints, necessitating earlier interventions compared to the general population. While total knee arthroplasty (TKA) for osteoarthritis in MHE with varus deformity is rarely reported in the literature, we present a case of a high body mass index (BMI) female with MHE and varus knee deformity successfully treated with TKA using a standard posterior stabilized implant, without additional constraints or extensive releases.

Case report: A 54-year-old Indian woman, homemaker presented to the clinic due to progressive left knee pain and varus deformity. Her BMI was 40. With no significant family history . The surgery was performed using a tourniquet. Using standard instrumentation for conventional TKA . The angle of bone resection was determined preoperatively through manual radiographic templating. The sizing of femoral component was done precariously since the anatomy of distal femur was altered with no prominent anterolateral ridge and an anterior referencing system was done to avoid notching. Tibial rotational alignment was based on anatomic landmarks. Patellofemoral tracking was excellent and did not require lateral retinacular release.

Conclusion: Careful attention to technical aspects, selection of implants and the unique anatomy involved, is crucial in planning this procedure. Ensuring proper balance of the ligaments tented by the osteochondromas and meticulous sizing of the femur are essential for favorable functional outcomes in such cases.

全膝关节置换术治疗膝关节骨性关节炎内翻畸形合并多发性遗传性外骨骼增生1例。
简介:多发性遗传性外生骨病(MHE)是一种常染色体显性遗传的遗传病,由外生骨病基因的点突变引起。膝关节畸形,如膝外翻,在MHE患者中很常见,通常局限于胫骨近端干骺端,偶尔累及股骨。膝骨软骨瘤可导致关节线倾斜,有助于早期发病的关节炎。角度增加也可能导致外侧髌骨半脱位和髌股主症,与一般人群相比,需要更早的干预。虽然文献中很少报道全膝关节置换术(TKA)治疗MHE伴膝内翻畸形的骨关节炎,但我们报告了一例高体重指数(BMI)的女性MHE伴膝内翻畸形患者,采用标准的后路稳定植入物,TKA成功治疗,没有额外的约束或广泛的松解。病例报告:一名54岁印度妇女,家庭主妇,因进行性左膝疼痛和内翻畸形而就诊。她的身体质量指数是40。没有明显的家族史。手术使用止血带进行。使用标准仪器进行常规TKA。术前通过手工x线摄影模板确定骨切除角度。股骨假体的大小不稳定,因为股骨远端解剖结构改变,没有明显的前外侧脊,并且做了一个前参考系统以避免缺口。胫骨旋转对准是基于解剖标志。髌股跟踪良好,不需要外侧支持带松解。结论:仔细注意技术方面,种植体的选择和所涉及的独特解剖结构,是计划该手术的关键。在这种情况下,确保由骨软骨瘤形成的韧带的适当平衡和股骨的精细大小对于良好的功能结果至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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