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[Bloch-Sulzberger's syndrome (Incontinentia pigmenti). Contribution with a case report].

Lourdes González Burgos, Beatriz Di Martino Ortíz, Mirtha Rodríguez Masi, Oilda Knopfelmacher, Lourdes Bolla de Lezcano

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Abstract

Incontinentia pigmenti (IP) is a rare genodermatosis. Skin lesions, that are present in all patients affected, evolve in stages. The first is the erythematous blistering stage, wich differential diagnosis includes a wide variety of diseases. We present a case of a female neonate with blisters present at birth, where the skin biopsy confirmed the diagnosis of IP.

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What this paper is about

Incontinentia pigmenti (IP) is a rare genodermatosis. Skin lesions, that are present in all patients affected, evolve in stages. The first is the erythematous blistering stage, wich differential diagnosis includes a wide variety of diseases. We present a case of a female neonate with blisters present at birth, where the skin biopsy confirmed the diagnosis of IP.

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OpenAlex reports 3 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Incontinentia pigmenti (IP) is a rare genodermatosis. Skin lesions, that are present in all patients affected, evolve in stages. The first is the erythematous blistering stage, wich differential diagnosis includes a wide variety of diseases. We present a case of a female neonate with blisters present at birth, where the skin biopsy confirmed the diagnosis of IP.

Key concepts: Genodermatosis, Incontinentia pigmenti, Medicine, Skin biopsy, Dermatology, Differential diagnosis, Skin lesion, Biopsy

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