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Pilomatrixoma: a common, benign childhood skin tumour.
OBJECTIVE: To review recent experience with pilomatrixoma, particularly with respect to diagnosis.
DESIGN: Chart review for an 8-year period.
SETTING: A university-affiliated children's hospital.
PATIENTS: Fifty children with 51 histologically proven pilomatrixomas.
INTERVENTION: Excision of the lesion.
MAIN OUTCOME MEASURES: Clinical presentation, diagnosis and pathological findings.
RESULTS: The clinical presentation was typically that of an asymptomatic superficial mass that increased slowly in size and was located in the head and neck (78%) or chest and upper limbs. In one case the mass increased rapidly over 2 weeks and changed in colour from red to purple with areas of pink and tan. The referring diagnosis was incorrect in 94% of cases, and the preoperative diagnosis was incorrect in 57%. Pathologically the tumours were situated in the dermis or subcutaneous tissue. None were cystic, but several had areas of calcification. None of the tumours recurred after excision, but two patients had multiple lesions at different locations and times.
CONCLUSIONS: Pilomatrixomas in children are simple to treat successfully but have variable clinical presentation. Early diagnosis is important so that unnecessary, aggressive surgery can be avoided.
DESIGN: Chart review for an 8-year period.
SETTING: A university-affiliated children's hospital.
PATIENTS: Fifty children with 51 histologically proven pilomatrixomas.
INTERVENTION: Excision of the lesion.
MAIN OUTCOME MEASURES: Clinical presentation, diagnosis and pathological findings.
RESULTS: The clinical presentation was typically that of an asymptomatic superficial mass that increased slowly in size and was located in the head and neck (78%) or chest and upper limbs. In one case the mass increased rapidly over 2 weeks and changed in colour from red to purple with areas of pink and tan. The referring diagnosis was incorrect in 94% of cases, and the preoperative diagnosis was incorrect in 57%. Pathologically the tumours were situated in the dermis or subcutaneous tissue. None were cystic, but several had areas of calcification. None of the tumours recurred after excision, but two patients had multiple lesions at different locations and times.
CONCLUSIONS: Pilomatrixomas in children are simple to treat successfully but have variable clinical presentation. Early diagnosis is important so that unnecessary, aggressive surgery can be avoided.
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