低磷血症:漏诊

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL International Journal of Academic Medicine Pub Date : 2021-01-01 DOI:10.4103/IJAM.IJAM_72_20
Tess Chamakkala, T. Gallagher
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引用次数: 0

摘要

低磷酸症是一种由组织非特异性碱性磷酸酶(ALP)缺陷引起的骨代谢紊乱。它在生命早期最为严重,但也可能出现在任何年龄,导致其成年后的诊断可能不足,而且通常不那么严重。这是一个42岁的女性病例,她向内分泌科询问她在双侧跖骨骨折的背景下ALP水平低,并被诊断为低磷酸酶。本病例报告旨在强调做出这种诊断的重要性,以避免可能有害的常用处方治疗。抗吸收疗法以及补充钙或维生素D可能会使疾病恶化。目前还没有食品和药物管理局批准的治疗成人低磷酸症的方法,但是asfotase和teriparatide是目前正在研究的两种很有前景的治疗方法。本文讨论了以下核心能力:基于实践的学习和改进,医学知识。
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Hypophosphatasia: A missed diagnosis
Hypophosphatasia is a disorder of bone metabolism due to defective tissue nonspecific alkaline phosphatase (ALP). It is most severe in early life but can present at any age, leading to a likely underdiagnosis of its adult, and commonly less severe, forms. This is the case of a 42-year-old female who presented to endocrinology asking about her low ALP levels in the setting of prior bilateral metatarsal fractures and was diagnosed with hypophosphatasia. This case report aims to highlight the importance of making this diagnosis in order to avoid commonly prescribed therapies that can be harmful. Antiresorptive therapies as well as supplementation with calcium or Vitamin D can potentially worsen the disease. There are no Food and Drug Administration-approved treatments for adult hypophosphatasia, but asfotase alfa and teriparatide are two promising therapies currently being studied. The following core competencies are addressed in this article: Practice-based learning and improvement, Medical knowledge.
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来源期刊
International Journal of Academic Medicine
International Journal of Academic Medicine Social Sciences-Education
CiteScore
1.10
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0.00%
发文量
8
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