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[低磷酸酯酶症患儿的牙科研究]

[Dental study of hypophosphatasic child].

作者信息

Takagi M, Takahashi M, Shimooka S

出版信息

Shigaku. 1989 Dec;77(4):1391-9.

PMID:2489352
Abstract

Hypophosphatasia is a hereditary disease characterized by congenital deficiency of tissue alkaline phosphatase. One of its dental features is the shedding of teeth. We have experienced a case which was referred to our clinic with the chief complaints of loss and shedding of lower deciduous central incisors and was diagnosed to be highly suspected of hypophosphatasia as a result of hematological examination at the pediatric clinic. As a result of close systemic and dental examination and further study of changes in the course for two and a half years, the following findings were obtained: 1. Low serum alkaline phosphatase level and hypercalcemia were the systemic findings of the disease. 2. There was no delayed ossification in terms of carpal bone age. 3. X-ray cephalography revealed no particular cephalic abnormality, except the lack of development of frontalis and mandibular. 4. Dental findings comprised marked resorption of upper alveolar bone in the front teeth area and pronounced instability of front deciduous teeth. 5. As for changes in oral symptoms, extraction of A because of pronounced instability was followed by spontaneous shedding of A. About one year later, A was extracted because of marked instability. At the time of this writing, A was slightly instable without any abnormality in the other teeth. 6. Pathohistological study of the extracted teeth disclosed only a little resorption of cement of root apex and dysgonic periodontium without any marked tissue changes.

摘要

低磷酸酯酶症是一种遗传性疾病,其特征为先天性组织碱性磷酸酶缺乏。其牙齿特征之一是牙齿脱落。我们遇到过一例,该患者因下乳切牙脱落和缺失为主诉前来我院就诊,经儿科门诊血液检查后被高度怀疑为低磷酸酯酶症。经过两年半的密切全身和口腔检查以及对病程变化的进一步研究,得出以下结果:1. 血清碱性磷酸酶水平降低和高钙血症是该疾病的全身表现。2. 腕骨年龄方面无骨化延迟。3. X线头影测量显示,除额骨和下颌骨发育不足外,无特殊头部异常。4. 口腔表现包括前牙区上牙槽骨明显吸收和乳前牙明显松动。5. 关于口腔症状的变化,因明显松动拔除A后,A自行脱落。大约一年后,因明显松动拔除A。在撰写本文时,A轻度松动,其他牙齿无异常。6. 对拔除牙齿的病理组织学研究显示,根尖牙骨质仅有少量吸收,牙周组织发育不良,无明显组织变化。

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