Pathological mandibular fracture complicated by osteonecrosis in an adult patient with pycnodysostosis: clinical report and review of the literature

被引:5
作者
Moroni, Alice [1 ]
Brizola, Evelise [1 ]
Di Cecco, Alessia [1 ]
Tremosini, Morena [1 ]
Sergiampietri, Marta [2 ]
Bianchi, Alberto [2 ,3 ]
Tappino, Barbara [4 ]
Piana, Maria [5 ]
Gnoli, Maria [1 ]
机构
[1] IRCCS Ist Ortoped Rizzoli, Dept Rare Skeletal Disorders, Bologna, Italy
[2] Univ Catania, CHIRMED Dept, Maxillo Facial Surg Unit, AOU Policlin San Marco, Catania, Italy
[3] Univ Catania, Dept Gen Surg & Med Surg Specialties, I-95124 Catania, Italy
[4] IRCCS Ist Giannina Gaslini, LABSIEM Lab Study Inborn Errors Metab, Genoa, Italy
[5] AOU Policlin San Marco, U O C Anat Patol II, Dipartimento Diagnost Immagini Lab, Catania, Italy
关键词
Pycnodysostosis; Mandibular fracture; Mandible osteonecrosis; Ultra-rare skeletal disease; Skeletal dysplasia; Acroosteolysis; POSITION PAPER; CTSK; JAW;
D O I
10.1016/j.ejmg.2023.104904
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.746T>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.
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页数:7
相关论文
共 27 条
[1]   Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features [J].
Arman, Ahmet ;
Bereket, Abdullah ;
Coker, Ajda ;
Kiper, Pelin Ozlem Simsek ;
Guran, Tulay ;
Ozkan, Behzat ;
Atay, Zeynep ;
Akcay, Teoman ;
Haliloglu, Belma ;
Boduroglu, Koray ;
Alanay, Yasemin ;
Turan, Serap .
ORPHANET JOURNAL OF RARE DISEASES, 2014, 9
[2]   Interventions for managing medication-related osteonecrosis of the jaw [J].
Beth-Tasdogan, Natalie H. ;
Mayer, Benjamin ;
Hussein, Heba ;
Zolk, Oliver .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2017, (10)
[3]   Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature review [J].
Bizaoui, Varoona ;
Michot, Caroline ;
Baujat, Genevieve ;
Amouroux, Cyril ;
Baron, Sabine ;
Capri, Yline ;
Cohen-Solal, Martine ;
Collet, Corinne ;
Dieux, Anne ;
Genevieve, David ;
Isidor, Bertrand ;
Monnot, Sophie ;
Rossi, Massimiliano ;
Rothenbuhler, Anya ;
Schaefer, Elise ;
Cormier-Daire, Valerie .
CLINICAL GENETICS, 2019, 96 (04) :309-316
[4]  
Caminha Raquel-D'Aquino-Garcia, 2020, J Clin Exp Dent, V12, pe725, DOI [10.4317/jced.56307, 10.4317/jced.56307]
[5]   Current Understanding of the Pathophysiology of Osteonecrosis of the Jaw [J].
Chang, J. ;
Hakam, A. E. ;
McCauley, L. K. .
CURRENT OSTEOPOROSIS REPORTS, 2018, 16 (05) :584-595
[6]   Osteomyelitis of the jaws in patients with pycnodysostosis: a systematic review [J].
de Franca, Gloria Maria ;
Felix, Fernanda Aragao ;
de Morais, Everton Freitas ;
de Souto Medeiros, Maurilia Raquel ;
de Macedo Andrade, Ana Claudia ;
Galvao, Hebel Cavalcanti .
BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY, 2021, 87 (05) :620-628
[7]   Clinical and genetic evaluation of Danish patients with pycnodysostosis [J].
Doherty, Mia Aa ;
Langdahl, Bente L. ;
Vogel, Ida ;
Haagerup, Annette .
EUROPEAN JOURNAL OF MEDICAL GENETICS, 2021, 64 (02)
[8]  
Donnarumma Michela, 2007, Hum Mutat, V28, P524, DOI 10.1002/humu.9490
[9]   Pycnodysostosis: a case report and literature review concerning oral and maxillofacial complications and their management [J].
El-Mahallawy, Yehia ;
Sweedan, Ahmed Ossama ;
Al-Mahalawy, Haytham .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY, 2021, 132 (04) :E127-E138
[10]  
Fassio A, 2017, REUMATISMO, V69, P9, DOI 10.4081/reumatismo.2017.983