Abstract

Calcinosis cutis is a term used to describe a group of disorders in which calcium deposits form in the skin and may be classified as dystrophic, metastatic, idiopathic or iatrogenic calcification, and calciphylaxis. Idiopathic calcinosis cutis occurs without any underlying tissue damage or metabolic disorder. In this paper, the authors report a new case of idiopathic calcinosis involving the medial canthus of the left eye that was mistaken for milia. An 18-year-old previously healthy male patient, presented with an asymptomatic whitish solitary tumour of the medial canthus of the left eye. The patient had no systemic or trauma history, and the serum levels of calcium and phosphorous were normal. An excisional biopsy was performed and histopathologic examination revealed subepidermal calcinosis. Calcinosis cutis is a rare condition that should be included in the differential diagnosis of a benign-appearing lesion of the face. While it can occur in patients with a history of inflammation, trauma, or hypercalcemia, its etiology can also be idiopathic.

Highlights

  • Calcinosis cutis is a rare disease characterized by the deposition of insoluble calcium salts in cutaneous tissue [1]

  • Calcinosis cutis is separated into five subtypes: dystrophic, metastatic, idiopathic, iatrogenic calcification, and calciphylaxis [2]

  • Metastatic calcification is characterized by an abnormal calcium and/or phosphate metabolism, leading to the precipitation of calcium in cutaneous and subcutaneous tissue

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Summary

Introduction

Calcinosis cutis is a rare disease characterized by the deposition of insoluble calcium salts in cutaneous tissue [1]. Introduction Calcinosis cutis is a rare disease characterized by the deposition of insoluble calcium salts in cutaneous tissue [1]. Idiopathic calcinosis cutis occurs in the absence of tissue injury or systemic metabolic effect. The authors report a new case of idiopathic calcinosis involving the medial canthus of the left eye which was mistaken for milia.

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