Alice Moroni, Evelise Brizola, Alessia Di Cecco, Morena Tremosini, Marta Sergiampietri, Alberto Bianchi, Barbara Tappino, Maria Piana, Maria Gnoli
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Pycnodysostosis is caused by biallelic loss of function variants in <em>CTSK</em> gene, coding the lysosomal protease cathepsin K. CTSK is involved in the degradation of bone matrix proteins, such as type I and type II collagen. In pycnodysostosis, this degradation is decreased, leading to increased bone density and bone fragility with pathological fractures and poor healing.</p><p>We present a clinical report of a female adult patient with typical pycnodysostosis phenotype. At the age of 52 years, she had a pathological spontaneous fracture of the right mandible complicated by osteonecrosis, treated with load bearing osteosynthesis. The direct sequencing of <em>CTSK</em> gene revealed the presence of the pathogenic homozygous variant c.746 T > A, (p.Ile249Asn), that confirmed the diagnosis of pycnodysostosis.</p><p>We also review the literature case series published to date, that suggest to always consider the diagnosis of pycnodysostosis in case of osteosclerosis, even in the absence of brachydactyly or short stature.</p><p>This report details the natural history of the disease in this patient, from childhood to adulthood, and highlights the importance of a quality of life assessment. 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引用次数: 0
摘要
Pycnodysostosis 是一种极其罕见的骨硬化性骨骼疾病,其特征是身材矮小、易骨折、远端趾骨骨质溶解和颅面特征(额突、鼻子突出、下颌角钝、小颌畸形)。牙齿异常(牙齿萌出延迟、牙齿发育不全、错牙合畸形、牙齿拥挤、乳牙滞留、釉质发育不全和龋齿增加)也很常见;由于骨代谢改变,患者患颌骨骨髓炎的风险增加,尤其是在拔牙或下颌骨骨折后。其他并发症包括阻塞性睡眠呼吸暂停、内分泌改变和全血细胞减少。CTSK 参与骨基质蛋白(如 I 型和 II 型胶原蛋白)的降解。在钙化性骨质疏松症患者中,这种降解作用减弱,导致骨密度增加、骨脆性增高、病理性骨折和愈合不良。我们报告了一名具有典型钙化性骨质疏松症表型的成年女性患者的临床病例。52岁时,她的右下颌骨发生病理性自发性骨折,并发骨坏死,经承重骨合成术治疗。对 CTSK 基因的直接测序显示,该基因存在致病性同源变异 c.746 我们还回顾了迄今为止发表的系列病例文献,这些文献建议在出现骨硬化症时,即使没有肱骨发育不全或身材矮小,也应始终考虑侏儒症的诊断。本报告详细介绍了该患者从童年到成年的自然病史,并强调了生活质量评估的重要性。此外,我们还描述了一例下颌骨骨坏死和自发性骨折的侏儒症患者,提请人们注意这些患者的颌面部并发症以及个性化随访的重要性。
Pathological mandibular fracture complicated by osteonecrosis in an adult patient with pycnodysostosis: Clinical report and review of the literature
Pycnodysostosis is an ultra-rare osteosclerotic skeletal disorder characterized by short stature, susceptibly to fractures, acroosteolysis of the distal phalanges, and craniofacial features (frontal bossing, prominent nose, obtuse mandibular angle, micrognathia). Dental abnormalities (delayed eruption of teeth, hypodontia, malocclusion, dental crowding, persistence of deciduous teeth, enamel hypoplasia, and increased caries) are also frequent; due to bone metabolism alteration, the patients have an increased risk for jaw osteomyelitis, especially after tooth extraction or mandible fracture. Other complications are obstructive sleep apnea, endocrine alterations and cytopenia. Pycnodysostosis is caused by biallelic loss of function variants in CTSK gene, coding the lysosomal protease cathepsin K. CTSK is involved in the degradation of bone matrix proteins, such as type I and type II collagen. In pycnodysostosis, this degradation is decreased, leading to increased bone density and bone fragility with pathological fractures and poor healing.
We present a clinical report of a female adult patient with typical pycnodysostosis phenotype. At the age of 52 years, she had a pathological spontaneous fracture of the right mandible complicated by osteonecrosis, treated with load bearing osteosynthesis. The direct sequencing of CTSK gene revealed the presence of the pathogenic homozygous variant c.746 T > A, (p.Ile249Asn), that confirmed the diagnosis of pycnodysostosis.
We also review the literature case series published to date, that suggest to always consider the diagnosis of pycnodysostosis in case of osteosclerosis, even in the absence of brachydactyly or short stature.
This report details the natural history of the disease in this patient, from childhood to adulthood, and highlights the importance of a quality of life assessment. In addition, we describe a case of mandibular osteonecrosis and spontaneous fracture in pycnodysostosis, drawing attention on the maxillofacial complications in these patients and on the importance of a personalized follow-up.
期刊介绍:
The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models.
Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as :
• Dysmorphology and syndrome delineation
• Molecular genetics and molecular cytogenetics of inherited disorders
• Clinical applications of genomics and nextgen sequencing technologies
• Syndromal cancer genetics
• Behavioral genetics
• Community genetics
• Fetal pathology and prenatal diagnosis
• Genetic counseling.