Evidence map›Paper›PMID 41065852›Full record

ArticlePediatric surgery international2025

Clinical features and surgical management of pilomatrixoma in children: a 332-case retrospective study.

Xiaoli Wang, Bingliang Li, Caihong Wang, Yu Tian, Xuesong Guo, Bin Wang

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Article in Pediatric surgery international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Xiaoli Wang *Department of Plastic and Burn Surgery, Shanxi Provincial Children's Hospital, Taiyuan, China.
Bingliang Li *Department of Neonatal Surgery, Shanxi Provincial Children's Hospital, Taiyuan, China.
Caihong WangDepartment of Pathology, Shanxi Provincial Children's Hospital, Taiyuan, China.
Yu TianDepartment of Plastic and Burn Surgery, Shanxi Provincial Children's Hospital, Taiyuan, China.
Xuesong GuoDepartment of Plastic and Burn Surgery, Shanxi Provincial Children's Hospital, Taiyuan, China. 18636632308@163.com.
Bin WangDepartment of Plastic and Reconstructive Surgery, Shanghai Key Laboratory of Tissue Engineering, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. wangbin1766@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAnalyze clinical characteristics and surgical outcomes of pediatric pilomatrixoma.

methodsA retrospective analysis was performed on the clinical data of 332 pediatric patients diagnosed with pilomatrixoma, who were admitted to the Shanxi Provincial Children's Hospital between January 2017 and December 2024. This cohort included a total of 350 tumors, with 11 cases presenting with 2 tumors, 2 cases with 3 tumors, and 1 case with 4 tumors. The analysis encompassed various parameters, including sex, age, disease course, tumor site, maximum diameter, ultrasound characteristics, and treatment modalities.

resultsPatients aged 4 months-17 years (male:female = 1:1.26; 147 M:185F), peak incidence 0-2 years. Tumors primarily facial (71.4%, n = 250), then neck (10.3%), head (8.9%), limbs (8.3%), and torso (1.1%). The tumors adhere to the skin to varying degrees, but are mobile over the underlying base; 52.3% (n = 183) had overlying skin discoloration; 0.9% (n = 3) ulcerated. Ultrasound predominantly showed hypoechoic lesions (82.6%, n = 289); echogenicity positively correlated with disease course (P < 0.05). Tumor diameter ranged 0.3-3.6 cm; most enlarged progressively (3 stable). All underwent complete surgical excision with cosmetic closure and postoperative anti-scar therapy. No recurrences or hypertrophic scarring occurred during follow-up. Histopathology confirmed diagnosis (basophilic basaloid cells, shadow cells, calcification).

conclusionPediatric pilomatrixoma shows slight female predominance, highest incidence under age 2, and favors the face. Hypoechoic ultrasound appearance is typical; size and echogenicity increase with longer duration. Early surgical intervention (within 6 months) minimizes incision length. Complete excision with cosmetic closure and anti-scar therapy achieves excellent aesthetic outcomes without recurrence.

Indexed as

Hair DiseasesPilomatrixomaSkin NeoplasmsAdolescentChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesTreatment OutcomeChildrenClinical featuresPilomatrixomaSurgical managementUltrasonography

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