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Investigation of the photosensitive child
1Department of Dermatology, Ninewells Hospital, Dundee, Scotland.
Insights
Childhood photosensitivity disorders are often diagnosed in dermatology clinics. Specialist phototesting is used for complex cases, requiring specific equipment and detailed analysis of light reactions over 48 hours.
Area of Science:
- Pediatric Dermatology
- Photobiology
- Immunodermatology
Background:
- Photosensitivity disorders in children are common.
- Diagnosis and management often occur in general dermatology settings.
- Specialist referral is sometimes necessary for definitive diagnosis.
Purpose of the Study:
- To outline the diagnostic process for childhood photosensitivity disorders.
- To describe the role and methodology of diagnostic phototesting.
- To highlight investigations aiding in clarifying clinical variants.
Main Methods:
- Phototesting using monochromator or provocation systems.
- Assessment of immediate and delayed readings over 48 hours.
- Inclusion of investigations like autoantibodies, porphyrin scans, and genetic studies.
Main Results:
- Specific patterns of wavelength dependency and response evolution characterize individual diseases.
- Phototesting requires specialized, often uncommon, equipment.
- Comprehensive data aids in clarifying common clinical variants.
Conclusions:
- Diagnostic phototesting is a crucial tool for photosensitivity disorders when clinical diagnosis is uncertain.
- Understanding wavelength dependency and response patterns is key.
- Integrated investigations improve diagnostic accuracy for rare genophotodermatoses.
Abstract:
Photosensitivity disorders in childhood frequently can be diagnosed and managed in the general dermatology clinic. Occasionally, when diagnostic doubt exists, referral to a specialist unit is required for diagnostic phototesting. Light testing equipment is fickle by nature, making such units uncommon. Phototesting using monochromator or provocation systems takes approximately 45 minutes. Immediate and delayed readings over the following 48 hours as appropriate are required to cover the diagnostic possibilities. Individual diseases are characterized by particular patterns of wavelength dependency and evolution of the abnormal response. Other investigations that may be required are autoantibodies to exclude lupus erythematosus, a porphyrin scan leading to full studies and, on occasion, cell mutation or survival, and chromosome studies for the rarer genophotodermatoses. Good investigative data frequently help clarify the common clinical variants.
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