Adult-onset hypophosphatasia diagnosed following bilateral atypical femoral fractures in a 55-year-old woman.

Q3 Medicine Clinical Cases in Mineral and Bone Metabolism Pub Date : 2017-09-01 Epub Date: 2017-12-27 DOI:10.11138/ccmbm/2017.14.3.347
John E Lawrence, Danish Saeed, Jonathan Bartlett, Andrew D Carrothers
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引用次数: 11

Abstract

We report the case of a 55-year-old woman who presented to the emergency department having woken from sleep with right sided thigh swelling. Pelvic radiographs revealed bilateral atypical subtrochanteric femoral fractures (ASFFs). In the two years leading up to this admission, the patient had experienced gradually increasing pain and weakness in her legs which had resulted in a decrease in her mobility from fully mobile to bed-bound. During this time a neurologist had organised a magnetic-resonance imaging (MRI) scan of the brain and spine which was normal. There was no history of bisphosphonate (BP) use. Historical and admission blood tests revealed a persistently low serum alkaline phosphatase (ALP), with all other results within normal limits. The patient was treated with intramedullary nailing of both femurs and histological analysis of bone reamings were characteristic of hypophosphatasia (HPP). The patient was independently mobilising with a walking frame on discharge. Subsequent genetic testing revealed bi-allelic pathogenic variants in the TNSALP gene: c.526G>A, p.(Ala176Thr) and c.1171C>T, p.(Arg391Cys). HPP is an inborn error in metabolism caused by mutation in the gene coding for tissue non-specific alkaline phosphatase (TNSALP), resulting in a decrease in serum ALP concentrations. The age at which it presents which can vary from childhood to middle age, with symptoms ranging from perinatal death to late-onset osteomalacia. In those patients who survive to adulthood, there is a predisposition to fractures, including ASFFs. Treatment with asfotase alfa (a bone-targeted, recombinant human TNSALP) has been approved for perinatal, infantile and paediatric-onset hypophosphatasia. This case emphasises the importance of viewing persistent low ALP as a 'red flag' in patients presenting with musculoskeletal symptoms. Timely diagnosis and treatment of HPP can reduce the risk of serious complications, such as those experienced by this patient.

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一名55岁女性双侧非典型股骨骨折后诊断为成人发病的低磷酸酶血症。
我们报告的情况下,55岁的妇女谁提出了急诊科从睡眠中醒来与右侧大腿肿胀。骨盆x线片显示双侧非典型股骨粗隆下骨折(ASFFs)。在入院前的两年中,患者的腿部疼痛和无力逐渐加重,导致其活动能力从完全活动到卧床。在此期间,一位神经科医生对正常的大脑和脊柱进行了核磁共振成像(MRI)扫描。无双膦酸盐(BP)使用史。病史和入院血液检查显示血清碱性磷酸酶(ALP)持续低,所有其他结果在正常范围内。患者接受了双侧股骨髓内钉治疗,骨组织分析显示为低磷血症(HPP)的特征。患者出院时可借助行走架独立活动。随后的基因检测显示TNSALP基因的双等位致病变异:c.526G>A, p.(Ala176Thr)和c.1171C>T, p.(Arg391Cys)。HPP是由组织非特异性碱性磷酸酶(TNSALP)基因编码突变引起的先天性代谢错误,导致血清ALP浓度下降。出现的年龄从儿童期到中年不等,症状从围产期死亡到迟发性骨软化。在那些存活到成年的患者中,有骨折的倾向,包括ASFFs。asfotase alfa(一种骨靶向的重组人TNSALP)已被批准用于围产期、婴儿和儿科发病的低磷酸症。本病例强调了将持续低ALP视为出现肌肉骨骼症状患者的“危险信号”的重要性。及时诊断和治疗HPP可以减少严重并发症的风险,例如本例患者所经历的并发症。
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来源期刊
Clinical Cases in Mineral and Bone Metabolism
Clinical Cases in Mineral and Bone Metabolism ENDOCRINOLOGY & METABOLISM-
CiteScore
2.60
自引率
0.00%
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0
期刊介绍: The Journal encourages the submission of case reports and clinical vignettes that provide new and exciting insights into the pathophysiology and characteristics of disorders related to skeletal function and mineral metabolism and/or highlight pratical diagnostic and /or therapeutic considerations.
期刊最新文献
From the Editor-in-Chief. Hypothyrodism as a risk factor of periodontitis and its relation with vitamin D deficiency: mini-review of literature and a case report. Atypical femur fractures: a distinctive tract of adult hypophosphatasia. Surgical treatment of neglected hip fracture in children with cerebral palsy: case report and review of the literature. Pitfalls in interpreting interventional studies for osteoporosis.
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