A CASE REPORT OF AGGRESSIVE SQUAMOUS CELL CARCINOMA IN PATIENTS WITH RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA
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Keywords

INHERITED EPIDERMOLYSIS BULLOSA
SQUAMOUS CELL CARCINOMA
RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA
NONHEALING WOUNDS

How to Cite

Kubanov, A., Karamova, A., Chikin, V., Monchakovskaya, Y., & Nefedova, M. (2020). A CASE REPORT OF AGGRESSIVE SQUAMOUS CELL CARCINOMA IN PATIENTS WITH RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA. Voprosy Onkologii, 66(5), 556–562. https://doi.org/10.37469/0507-3758-2020-66-5-556-562

Abstract

Recessive dystrophic epidermolysis bullosa (RDEB) is an orphan genetic skin disease which is caused by mutations in COL7A1 gene. COL7A1 encodes collagen VII - a major component of anchoring fibrils which sustain the dermal-epidermal junction. Non-healing wounds typically are presented in patients with RDEB. They predispose cutaneous squamous cell carcinoma (SCC) development. RDEB-associated SCC is a rapidly growing tumor of aggressive nature which generally arises at young age and results in early mortality. This article reports 2 patients with RDEB-associated SCCs.
https://doi.org/10.37469/0507-3758-2020-66-5-556-562
PDF (Русский)

References

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