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10 April 2025 : Case report  Saudi Arabia

[In Press] Earlobe Pilomatrixoma in Children: Clinical Features and Surgical Management

Challenging differential diagnosis, Educational Purpose (only if useful for a systematic review or synthesis)

Abdullah Alkhaldi12ABEF, Reem Althwanay3ABEF, Abdullah Saad Alsalamah12ABEF, Abdulelah Mashhor Aldakheel4BDEF, Baraa Awad12ABEF, Mohammed Halawani12ABEF

DOI: 10.12659/AJCR.946474

Am J Case Rep In Press; DOI: 10.12659/AJCR.946474  

Available online: 2025-04-10, In Press, Corrected Proof

Publication in the "In-Press" formula aims at speeding up the public availability of the pending manuscript while waiting for the final publication. The assigned DOI number is active and citable. The availability of the article in the Medline, PubMed and PMC databases as well as Web of Science will be obtained after the final publication according to the journal schedule

Abstract

BACKGROUND
Pilomatrixomas are benign skin tumors that tend to occur in children. They most commonly arise in the head and neck region, but their appearance in the ear, especially the earlobe, is rare. Clinically, these lesions present as firm, non-tender nodules, occasionally with a reddish or bluish tint. Given the lesions’ typical features, experienced clinicians may opt for surgical excision without extensive workup. Still, diagnosis can be challenging when the lesion is located in an unusual site, like the auricle, where it can resemble other skin conditions. In this report, we describe a case of earlobe pilomatrixoma and outline its clinical presentation, surgical management, and histopathological findings.
CASE REPORT
A 6-year-old girl presented with a painless, stable mass on her right earlobe, first noticed at the age of 3 years. Physical examination revealed a firm, non-tender, well-circumscribed, mobile lesion, with no overlying skin changes or history of trauma. No previous imaging or investigations were conducted. After discussion, surgical excision was performed. Histopathological analysis showed alternating eosinophilic and basophilic calcified areas, abundant anucleate eosinophilic ghost cells, and multinucleated giant cells, confirming pilomatrixoma. Notably, basaloid and transitional cells were absent, suggesting lesion maturity.
CONCLUSIONS
This case emphasizes the importance of considering pilomatrixoma in the differential diagnosis of pediatric head and neck masses and how it might even present in some unusual locations, such as the auricle. Recognizing its clinical features can facilitate effective management while minimizing unnecessary diagnostic tests. In this case, we highlighted an efficient approach and raised awareness of pilomatrixoma’s distinctive presentation.

Keywords: Ear Auricle; Pediatrics; Pilomatrixoma

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923