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Pilomatrixoma Presenting as a Rapidly Expanding Mass of the Infant Nasion
Lauren C Nigro1, Christine E Fuller1, Jennifer L Rhodes1
1Virginia Commonwealth University, West Hospital, Richmond, Virginia.
Insights
This study reports a rare case of pilomatrixoma in an 11-month-old infant, highlighting its atypical presentation on the nasion. Complete surgical excision proved effective for this benign hair follicle neoplasm.
Area of Science:
- Dermatology
- Pediatric Oncology
- Pathology
Background:
- Pilomatrixomas are benign neoplasms arising from hair follicle cells.
- Typically present as solitary masses on the head and neck, common in children but rare in infants.
- Atypical presentations can challenge preoperative diagnosis.
Purpose of the Study:
- To present a rare case of pilomatrixoma in an 11-month-old infant.
- To describe the management of an atypical pilomatrixoma on the midline nasion.
- To review the literature on pilomatrixomas, emphasizing unusual infantile cases.
Main Methods:
- Case presentation of an 11-month-old infant with an atypical nasion mass.
- Utilized computed tomography (CT) and magnetic resonance imaging (MRI) for preoperative assessment.
- Diagnosis confirmed by histopathological examination post-surgical excision.
- Conducted a comprehensive literature review on pilomatrixomas.
Main Results:
- The patient presented with an atypical pilomatrixoma not correlating with typical descriptions.
- Preoperative imaging (CT, MRI) did not lead to a definitive diagnosis.
- Histopathology confirmed pilomatrixoma after surgical excision.
- The patient showed no evidence of recurrence post-treatment.
Conclusions:
- This is the first reported case of a pilomatrixoma presenting on the midline nasion in an infant.
- Clinicians should consider pilomatrixoma in the differential diagnosis of pediatric head and neck skin lesions, even with atypical presentations.
- Complete surgical excision is the definitive and effective treatment for pilomatrixoma.
Abstract:
Objective: Pilomatrixomas are benign neoplasms originating from the cells of hair follicles. They typically present as a slowly enlarging, solitary mass on hair-bearing areas of the head and neck. While a common childhood lesion, pilomatrixomas are unusual in infancy. Our objective is to present an atypical pilomatrixoma located on the midline nasion of an 11-month-old as such a lesion and its management has not been previously described. Methods: Despite preoperative diagnostic imaging, including computed tomography and magnetic resonance imaging, the diagnosis was not made until examination by pathology after complete surgical excision. We also completed a thorough review of the literature pertaining to pilomatrixomas, which is presented in a concise fashion. Results: Our patient's clinical presentation did not correlate with traditional descriptions in the literature, skewing preoperative diagnosis. However, surgical management was ultimately appropriate and effective. To date, the patient has not demonstrated evidence of recurrence. Conclusion: We believe that this is the first such reported presentation of a pilomatrixoma. Given its incidence, we encourage readers to consider this diagnosis when evaluating similar pediatric skin lesions of the head and neck. Complete surgical excision is the definitive treatment.
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