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Metacarpal Small Incision for Carpal Tunnel Syndrome
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When a Little Wrist Raises big Questions: A Case of Idiopathic Pediatric Carpal Tunnel Syndrome
Corentin Stavart1,2,3, Stéphanie Moortgat4, Christine Galant5,6
1Department of Pediatrics, CHU UCL Namur Godinne, Yvoir, Belgium.
Insights
Idiopathic carpal tunnel syndrome (CTS) is rare in children. This case highlights the importance of a multidisciplinary diagnostic approach for pediatric CTS to prevent nerve damage and identify underlying conditions.
Area of Science:
- Pediatric Neurology
- Peripheral Neuropathy
- Surgical Case Study
Background:
- Carpal tunnel syndrome (CTS) is a common peripheral neuropathy in adults.
- Pediatric CTS is typically secondary to underlying conditions, unlike adult multifactorial cases.
Purpose of the Study:
- To present a case of idiopathic carpal tunnel syndrome in an 11-year-old girl.
- To emphasize the diagnostic and etiological workup for pediatric CTS.
- To highlight the importance of early recognition and multidisciplinary care.
Main Methods:
- Comprehensive investigations including imaging, metabolic and genetic testing, histopathology, and electroneuromyography (EMG).
- Surgical intervention for carpal tunnel release.
- Post-operative ultrasonography and EMG follow-up.
Main Results:
- Idiopathic CTS was diagnosed after excluding other causes.
- Surgery confirmed complete decompression, with improved but persistently abnormal EMG findings.
- The patient experienced clinical improvement with residual paresthesia.
Conclusions:
- Pediatric CTS requires a thorough diagnostic evaluation, including a multidisciplinary approach.
- Early diagnosis is crucial to prevent irreversible median nerve damage.
- Identifying underlying systemic causes is essential for comprehensive care and improved outcomes.
Abstract:
BackgroundCarpal tunnel syndrome (CTS) is the most common peripheral neuropathy in adults but is rarely encountered in children. Pediatric CTS is usually secondary to specific underlying conditions, contrasting with the largely multifactorial nature of adult cases.Case presentationWe report the case of a right-handed 11-year-old girl who developed CTS. Extensive investigations including imaging, metabolic and genetic testing, as well as histopathologic and electroneuromyography analysis, excluded metabolic, anatomical, tumoral, and traumatic causes, leading to the diagnosis of an idiopathic form. After surgery, ultrasonography confirmed a complete decompression whereas EMG was improved but remained persistently abnormal. The patient was clinically improved but still had slight residual paresthesia.ConclusionThis case underlines the diagnostic and etiologic workup of CTS in children. Early recognition is essential to prevent irreversible median nerve damage and to uncover potential systemic underlying causes. A multidisciplinary approach, combining detailed family and medical history, clinical examination, imaging, electrophysiology, and targeted metabolic and genetic testing, is fundamental to ensure accurate diagnosis, comprehensive care, and improved outcomes.
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