Idiopathic Juvenile Osteoporosis: A Case Report and Literature Review

This case report describes the rare occurrence of idiopathic juvenile osteoporosis (IJO) in an 11-year-old boy with bone fragility and fractures, particularly in the thoracic and lumbar vertebrae. After excluding discernible underlying causes, the diagnosis was confirmed using clinical and radiological assessments. Treatment commenced with oral bisphosphonates, leading to notable bone mineral density (BMD) improvements and the absence of subsequent fractures. IJO presents diagnostic challenges owing to its multifaceted nature, necessitating the exclusion of other common causes of pediatric osteoporosis. Although the pathophysiology of IJO remains poorly understood, this case underscores the potential efficacy of bisphosphonate therapy in managing the condition and improving patient outcomes. Notably, the patient's symptoms ameliorated as puberty commenced, aligning with the typical IJO patterns reported in the literature. Although the long-term impact of bisphosphonate treatment in pediatric IJO cases warrants further investigation, this case exemplifies the potential to enhance the quality of life of affected individuals.

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Publication Details

Journal
Cureus
Published
2024-09-01
DOI
https://doi.org/10.7759/cureus.68361
Citations
1
Primary Topic
Connective tissue disorders research
Type
article
Field-Weighted Citation Impact
0.55
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article

Idiopathic Juvenile Osteoporosis: A Case Report and Literature Review

S Shimazaki, Junichi Sato
1 citations
Cureus
Connective tissue disorders research
0.55
article

Idiopathic Juvenile Osteoporosis: A Case Report and Literature Review

S Shimazaki, Junichi Sato
article en
1 citations

Abstract

This case report describes the rare occurrence of idiopathic juvenile osteoporosis (IJO) in an 11-year-old boy with bone fragility and fractures, particularly in the thoracic and lumbar vertebrae. After excluding discernible underlying causes, the diagnosis was confirmed using clinical and radiological assessments. Treatment commenced with oral bisphosphonates, leading to notable bone mineral density (BMD) improvements and the absence of subsequent fractures. IJO presents diagnostic challenges owing to its multifaceted nature, necessitating the exclusion of other common causes of pediatric osteoporosis. Although the pathophysiology of IJO remains poorly understood, this case underscores the potential efficacy of bisphosphonate therapy in managing the condition and improving patient outcomes. Notably, the patient's symptoms ameliorated as puberty commenced, aligning with the typical IJO patterns reported in the literature. Although the long-term impact of bisphosphonate treatment in pediatric IJO cases warrants further investigation, this case exemplifies the potential to enhance the quality of life of affected individuals.

CureusVol. 16(9)
Funabashi Municipal Medical Center (JP)
Gender equality
Openalex Percentile: Top 26%
Connective tissue disorders research
0.55
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