Progressive symmetric erythrokeratoderma: A rare case report Patro N, Panda M, Dash M, Jena SS, Mohapatra M, - J Indian Prosthodont Soc

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Progressive symmetric erythrokeratoderma: A rare case report Nibedita Patro¹, Maitreyee Panda¹, Mrutunjay Dash², Subhransu Sekhar Jena³, Madhuchhanda Mohapatra¹ ¹ Department of Skin and VD, IMS and SUM Hospital, SOA University, Bhubaneswar, Odisha, India ² Department of Paediatrics, IMS and SUM Hospital, SOA University, Bhubaneswar, Odisha, India ³ Department of Neurology, IMS and SUM Hospital, SOA University, Bhubaneswar, Odisha, India Correspondence Address: Nibedita Patro, Department of Skin and VD, IMS and SUM Hospital, SOA University, Bhubaneswar - 751 003, Odisha India Source of Support: None, Conflict of Interest: None DOI: 10.4103/2319-7250.184334

Erythrokeratodermas are a rare group of genetic disorders presenting early in childhood as erythematous, hyperkeratotic plaques on the skin. There may be associated neurological involvement. A 12-year-old boy presented with symmetric keratotic plaques on the body since infancy. Psoriasis and pityriasis rubra pilaris were ruled out after histopathological examination of the skin. We are reporting a case of progressive symmetric erythrokeratoderma with classical lesions but can be missed due to unawareness.

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