定制肱骨反向肩关节置换术及术中GPS导航治疗一例罕见的单侧髋关节和肩部发育不良伴骨髓嵌合PTEN截断变异:病例报告

Giovanni Battista Colasanti, Elisa Troiano, Alice Giulia De Sensi, Laura Di Sarno, Alessandra Renieri, Nicola Mondanelli, Sefano Giannotti
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引用次数: 0

摘要

关节发育不良一直是假肢外科医生面临的巨大挑战。如果采用标准方法,常见的解剖标志改变和发育不良关节周围软组织解剖结构的颠覆是可能造成困难的问题。与解决与发育不良相关的功能问题一起,了解其根本原因是至关重要的。DNA分析通常通过血液取样进行;然而,如果在血液成分中没有检测到嵌合现象,这可能会导致误诊。遗传疾病的病因可以通过全外显子组测序和体细胞嵌合体检测来进一步研究,体细胞嵌合体被认为是遗传疾病本身的一个基本因素。在本研究中,我们报告了一例罕见的单侧发育不良患者,该患者位于左髋股关节和盂肱关节,并在我们中心进行了反向肩关节置换术。由于肩关节解剖的特殊性,我们必须设计一种混合的定制和导航入路,通过定制的假体柄和专用的患者专用仪器,使用术中GPS导航进行肩关节假体。此外,对术中收获的骨髓进行了一项遗传学研究,这对理解不典型增生的表观遗传学基础至关重要。事实上,该患者的血检结果为阴性,但PTEN c.781C >T (p.(Gln261 *))在骨髓中分析的序列中占12%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Reverse Shoulder Arthroplasty Implantation With Custom-Made Humerus and Intraoperative GPS Navigation in a Rare Case of Unilateral Hip and Shoulder Dysplasia Associated With a Bone Marrow Mosaic PTEN Truncating Variant: Case Report
Joint dysplasias always represent a great challenge for prosthetic surgeons. The common altered anatomical landmarks and the subversion of the anatomy of soft tissues surrounding the dysplastic joint are problems that can cause difficulties if approached with standard methods. Together with the resolution of functional issues related to dysplasia, the understanding of the underlying cause is fundamental. DNA analysis is generally performed via blood sampling; however, this might lead to misdiagnosis in case mosaicism is not detected in blood components. The etiology of genetic diseases can be further examined by means of whole exome sequencing and the detection of somatic mosaicism, recognized as a fundamental contributor to genetic diseases themselves. In this study, the clinical case of a patient suffering from a rare unilateral dysplasia localized to the left coxo-femoral and glenohumeral joint and treated at our center for reverse shoulder arthroplasty is reported. By virtue of the glenohumeral anatomical peculiarities, we had to devise a hybrid custom-made and navigated approach by means of a custom-made prosthetic stem and dedicated patient-specific instrumentation, using intraoperative GPS navigation for glenoid prosthesis. In addition, a genetic study was conducted on intraoperatively harvested bone marrow, which proved to be crucial in understanding the epigenetic basis of dysplasia. In fact, the patient resulted negative in blood but positive for a truncating variant of PTEN c.781C > T (p.(Gln261 *)) in 12% of the sequence analyzed in the bone marrow.
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