Journals / Güncel Pediatri / 2019 / Cilt: 17 Sayı: 3

Two siblings diagnosed with epidermodysplasia verrusiformis: Case report Epidermodysplasia verrusiformis

Epidermodisplazia Verrusiformis Tanısı Konulan İki Kardeş: Olgu Sunumu Epidermodisplazia Verrusiformis

Pages
435–441
Publication Date
2019-12-02
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

For this reason, we think that it is appropriate for the patients to be protected from the sun and closely followed by the dermatologists.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Epidermodisplasia verrusiformis (Lewandowsky Lutz syndrome) is a rare, autosomal recessive genodermatosis characterized by a defect in cellular immunity and increased susceptibility to Human Papillomavirus infection.
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Key Findings & Data:One of the siblings is a 13-year-old girl and the other is a 15-year-old.
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Conclusion & Impact:For this reason, we think that it is appropriate for the patients to be protected from the sun and closely followed by the dermatologists.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:epidermodisplazis verrusiformis · Human Papillomavirüs · cutaneous malignancy

Abstract

Epidermodisplasia verrusiformis (Lewandowsky Lutz syndrome) is a rare, autosomal recessive genodermatosis characterized by a defect in cellular immunity and increased susceptibility to Human Papillomavirus infection. Typical clinical findings include pityriasis versicolor-like macules, flat wart-like papules, psoriasiform red papules, and pigmented keratotic lesions resembling seborrheic keratosis. Cutaneous malignancies can develop on sun-exposed regions. Herein, we present two siblings diagnosed with Epidermodisplasia verrusiformis. One of the siblings is a 13-year-old girl and the other is a 15-year-old. There were skin lesions on the hands, face and neck for five years. In patients diagnosed with Epidermodispazia verruculiformis, particularly in the sun-exposed areas, cutaneous malinites can develop in younger ages. For this reason, we think that it is appropriate for the patients to be protected from the sun and closely followed by the dermatologists.

Özet

 Epidermodisplazis verrusiformis (Lewandowsky Lutz sendromu) nadir görülen, otozomal resesif geçen, hücresel immunitedeki defekt ile karakterize ve Human Papillomavirüs enfeksiyonuna duyarlılığın arttığı bir genodermatozdur. Tipik klinik bulgular arasında pitriyazis versikolora benzer maküller, düz siğil benzeri papüller, psöriaziform kırmızı papüller ve seboreik keratoza benzeyen pigmente keratotik lezyonlar bulunur. Güneş gören bölgelerde kütanöz maligniteler gelişebilmektedir. Burada Epidermodisplazis verrusiformis tanısı konulan iki kardeş olgu sunulmaktadır. Kardeşlerden biri 13 yaşında kız, diğeri ise 15 yaşında erkekti. El, yüz ve boyunlarında beş yıldan beri olan cilt lezyonları mevcuttu. Epidermodispazia verrusiformis hastalarında özellikle güneş gören bölgelerde, erken yaşlarda kütanöz maliniteler gelişebilmektedir. Bu nedenle hastaların güneşten korunmasının ve dermatologlar tarafından yakın takibinin uygun olduğunu düşünmekteyiz.

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Cite This Article

Karapınar, T., Erdoğan, H. K., Bulur, İ., Saraçoğlu, Z. N., Dündar, E. (2019). Two siblings diagnosed with epidermodysplasia verrusiformis: Case report Epidermodysplasia verrusiformis. Güncel Pediatri, Cilt: 17 Sayı: 3, 435–441. https://ajindex.com/articles/991873

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