Pilomatrixoma (Calcifing Epithelioma of Malberbe), Case Study

Pilomatrixoma, also known as calcifying epithelioma of Malberbe, is a rare, benign skin tumor derived from hair follicle matrix cells. It predominantly affects young children but can occur across all age groups, with a slight female preponderance. This study presents the case of a 7-year-old female with a gradually enlarging mass on the left arm, diagnosed as pilomatrixoma following surgical excision and histopathological analysis. Pilomatrixoma typically manifests as a solitary, firm, skin-colored or purplish lesion, most commonly on the head, neck, or upper extremities. It is characterized by calcification within the lesion, often presenting the "tent sign," and is generally asymptomatic but can occasionally cause tenderness. Dermoscopy, imaging (e.g., ultrasound, X-ray), and biopsy are critical diagnostic tools, with histological findings revealing basophilic cells, shadow cells, and calcium deposits. The lesion in this case was excised surgically, a treatment that remains the standard to confirm diagnosis, alleviate cosmetic concerns, and prevent rare complications like malignant transformation. Although rare, pilomatrixoma may recur or become pilomatrix carcinoma. This research underscores the importance of early diagnosis and treatment of pilomatrixoma for favorable outcomes.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2024-11-30
DOI
https://doi.org/10.5281/zenodo.14251570
Primary Topic
Cancer and Skin Lesions
Type
article
Field-Weighted Citation Impact
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article

Pilomatrixoma (Calcifing Epithelioma of Malberbe), Case Study

Zenodo (CERN European Organization for Nuclear Research)
Cancer and Skin Lesions
article

Pilomatrixoma (Calcifing Epithelioma of Malberbe), Case Study

article en

Abstract

Pilomatrixoma, also known as calcifying epithelioma of Malberbe, is a rare, benign skin tumor derived from hair follicle matrix cells. It predominantly affects young children but can occur across all age groups, with a slight female preponderance. This study presents the case of a 7-year-old female with a gradually enlarging mass on the left arm, diagnosed as pilomatrixoma following surgical excision and histopathological analysis. Pilomatrixoma typically manifests as a solitary, firm, skin-colored or purplish lesion, most commonly on the head, neck, or upper extremities. It is characterized by calcification within the lesion, often presenting the "tent sign," and is generally asymptomatic but can occasionally cause tenderness. Dermoscopy, imaging (e.g., ultrasound, X-ray), and biopsy are critical diagnostic tools, with histological findings revealing basophilic cells, shadow cells, and calcium deposits. The lesion in this case was excised surgically, a treatment that remains the standard to confirm diagnosis, alleviate cosmetic concerns, and prevent rare complications like malignant transformation. Although rare, pilomatrixoma may recur or become pilomatrix carcinoma. This research underscores the importance of early diagnosis and treatment of pilomatrixoma for favorable outcomes.

Zenodo (CERN European Organization for Nuclear Research)
Baghdad Medical City (IQ), Iraqi University (IQ)
Openalex Percentile: Top 46%
Cancer and Skin Lesions
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Pilomatrixoma (Calcifing Epithelioma of Malberbe), Case Study · Zenodo (CERN European Organization for Nuclear Research) (2024) | TGRS Research Map | TGRS