关键词: Enostoses Osteopoikilosis Sclerosing bone dysplasia, case report

来  源:   DOI:10.1016/j.ijscr.2021.106447   PDF(Pubmed)

Abstract:
BACKGROUND: Osteopoikilosis (OPK) is an extremely rare benign condition with sclerosing bony dysplasia and multiple benign enostoses. OPK is usually asymptomatic and is typically an incidental finding on imaging studies for unrelated conditions.
METHODS: We presented a case of OPK in a 7-year-old female with hallux valgus, shortening and deformity of second and third metatarsals in the right foot. These abnormalities were observed on clinical findings with X-ray imaging, and osteopoikilosjs was confirmed by histopathology. The deformities were treated with surgical intervention, and the patient\'s condition was followed for 3 months until the patient walked and removed the gypsum.
CONCLUSIONS: OP is a rare, benign disease that rarely causes bony deformities. It is diagnosed clinically and radiographically, so that the deformities are treated only surgically. Follow-up is necessary to assess the movement of the limb.
CONCLUSIONS: The distinctive thing that can be added to the medical literature is that it is possible for osteopoikilosis to cause bone deformities at an early age.
摘要:
背景:骨质疏松症(OPK)是一种极其罕见的良性疾病,伴有硬化性骨发育不良和多发性良性结瘤。OPK通常无症状,通常是不相关疾病的影像学检查的偶然发现。
方法:我们介绍了一例7岁女性外翻患者的OPK,右脚第二和第三跖骨的缩短和畸形。这些异常在X线成像的临床表现上观察到,骨polikilosjs经组织病理学证实。畸形接受手术治疗,对患者的病情随访3个月,直到患者行走并取出石膏。
结论:OP是一种罕见的,很少引起骨畸形的良性疾病。它被诊断为临床和影像学检查,所以畸形只能通过手术治疗。随访对于评估肢体的运动是必要的。
结论:可以添加到医学文献中的独特之处在于,骨质疏松可能在早期引起骨畸形。
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