Affiliation:
1. Kempegowda Institute of Medical Sciences & Research Center, Bangalore, Karnataka, India
Abstract
Pachyonychia congenital (PC), is a rare genetic disorder, autosomal dominant, disorder of keratinization. This condition is characterized by cutaneous manifestation mainly hyperkeratosis of skin and mucosae and hypertrophy of nails. In this condition, almost 50% of the patients will have oral leukokeratosis. The case report here is of a 15 years old girl, presented with dystrophic, thickened fingernails and toenails with subungual hyperkeratosis, palmoplantar keratoderma, hyperkeratotic plaques in buccal mucosae. Histological examination shows acanthosis, parakeratosis and ballooning of epithelial cells, these features were consistent leukokeratosis, and has been diagnosed as Pachyonychia Congenita type 1. This is a rare condition hence, has been reported.
Publisher
IP Innovative Publication Pvt Ltd
Reference16 articles.
1. Rathore P K, Khuller V, Das A, Pachyonychia Congenita Type !: Case report and Review of the Literature.Indian J Dermatol 2016;61(2):196-9
2. Muller C, On the causes of congenital onychogryphosis.Men Med Wochenschr 1904;49:2180-2
3. Jadassohn J, Lewandowsky F, Berlin: Urban und Schwarzenberg. Pachonychia Congenita. 1st Edn..Keratosis disseminate circumscripta (follicularis).29-31
4. Sachidanand S, Oberoi C, Imandar AC, IADVL Textbook of dermatology. 4th ed. 2015;1:393-5
5. Sravanthi A, Srivalli P, Gopal KV, Rao TN, Pachyonchia Congenita with late onset (PC tarda).Indian J Dermatol 2016;7(4):278-80