Chronic Knee Pain is the Paramount Presentation in Patients with Nail-Patella Syndrome

A. Kaissi
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引用次数: 0

Abstract

Background: Arthralgia in connection with patellar instability have been studied thoroughly in a number of pediatric and adult patients. Small and dysplastic patellae accompanied by hypoplasia of the lateral femoral condyle may results in recurrent subluxation or dislocation of the patellae, knee discomfort and pain. We aimed to detect the underlying etiology of every single patient. Patients and Methods: A total of seven children presented with long term painful knee joints have been refered from the departments of rheumatology. We added adult female patient of a-35-years-old. She was a chronic client of rheumatology clinics since her postadulthood. In addition to her early life knee pain. Recently she experienced additional chronic pain of the groin (located at the posterior buttocks). All our patients showed episodes of knee pain with variable intensity as a constant complaint and all received antirheumatic treatments for years despite the negative results of the implemented tests. In order to commence the diagnostic process, clinical and radiological phenotypic characterization were the main core of our stratregy followed by molecular genetic confirmation. Results: Seven unrelated children (aged from 8-17 years old) were consistent with the diagnosis of Nail- Patella syndrome. The adult female patient of a-35-years-old- manifested patellar instability since her early childhood. Her clinical phenotype was totally compatible with the diagnosis of Nail-Patella syndrome. Surprisingly, the clinical examination of the female patient and the standing AP pelvis radiograph revealed massive encroachment of the medial aspect of the femoral neck and the lesser trochanters onto the ischium. The latter resulted in the diagnosis of Ischiofemoral Impingement (IFI) syndrome. Her genetic tests showed heterozygous mutation in the LIM-homeodomain protein LMX1B on chromosome 9q33. Conclusion: Arthralgia associated with abnormal gait (mostly antalgic gait and waddling gait) was the paramount clinical presentation in all our patients. Dysplasia of the nails and patellar instability were the characteristic clinical findings in our patients with the definite diagnosis of osteo-onychodysplasia syndrome. We approached to the diagnosis from the first session of clinical examination. Interestingly, the constant groin pain in the adult female patient which has been totally overlooked by other instutions, were in favor of the diagnosis of Ischiofemoral Impingement (IFI) syndrome. As well as the existing abnormality of the elbows associated with defective pronation and supination as due to impingement of the olecranon. The task of establishing the diagnostic process in complex clinical conditions is the most challenging. Sadly speaking, none of the aforemnetioned dignostic criteria attracted the attention of dozens of clinicians. Admistering medications to overcome knee pain through dozens of useless laboratory tests were the main false issue. Clinicians who are actively involved in clinical diagnosis with minimal dependency on laboratory aid are generally at the forefront of their medical fields.
慢性膝关节疼痛是指甲-髌骨综合征患者的首要表现
背景:与髌骨不稳定相关的关节痛已经在许多儿童和成人患者中进行了深入的研究。小而发育不良的髌骨伴股外侧髁发育不全可导致复发性髌骨半脱位或脱位,膝关节不适和疼痛。我们的目标是发现每一个病人的潜在病因。患者和方法:从风湿病科转介了7例长期膝关节疼痛的患儿。我们加入了a-35岁的成年女性患者。自成年后,她一直是风湿病诊所的长期客户。除了她早年的膝盖疼痛。最近,她又经历了腹股沟(位于臀部后部)的慢性疼痛。我们所有的患者都表现出不同强度的膝关节疼痛发作,作为一种持续的主诉,尽管实施的测试结果为阴性,但所有患者都接受了多年的抗风湿病治疗。为了开始诊断过程,临床和放射学表型表征是我们策略的主要核心,其次是分子遗传学确认。结果:7例无亲缘关系患儿(年龄8-17岁)符合甲-髌骨综合征的诊断。成年女性患者a-35岁-自童年早期就表现出髌骨不稳。她的临床表型完全符合指甲-髌骨综合征的诊断。令人惊讶的是,女性患者的临床检查和站立AP骨盆x线片显示股骨颈内侧和小粗隆向坐骨的严重侵犯。后者导致坐骨股撞击(IFI)综合征的诊断。基因检测显示9q33号染色体上lim同源结构域蛋白LMX1B杂合突变。结论:关节痛伴异常步态(以疼痛步态和蹒跚步态为主)是本组患者最主要的临床表现。指甲发育不良和髌骨不稳是我们确诊为骨甲发育不良综合征患者的典型临床表现。我们从第一次临床检查开始进行诊断。有趣的是,成年女性患者持续的腹股沟疼痛被其他机构完全忽视,这有利于坐骨股撞击(IFI)综合征的诊断。以及现有的肘关节异常,由于鹰嘴撞击导致的旋前和旋后缺陷。在复杂的临床条件下建立诊断过程的任务是最具挑战性的。遗憾的是,上述的诊断标准都没有引起许多临床医生的注意。通过几十次无用的实验室测试来治疗膝盖疼痛是主要的错误问题。积极参与临床诊断,对实验室援助依赖最小的临床医生通常处于其医学领域的前沿。
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