Parakeratosis pustulosa is a cutaneous condition which is exclusively seen in children, usually involving one finger, most commonly the thumb or index finger, with the affected nail showing subungual hyperkeratosis and onycholysis.[1]: 662 [2]: 1026 [2]
The cause of parakeratosis pustulosa is unknown however there have been several diseases linked to it and it does not seem to be genetic.
Parakeratosis pustulosa is diagnosed based on clinical characteristics and the exclusion of other conditions.
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Transcription
Signs and symptoms
Parakeratosis pustulosa is most commonly seen in children as an eczematoid eruption near the free margin of the nail that extends to the dorsal nail fold. Under the free margin of the nail, hyperkeratosis causes the nail plate to pull up and results in a deformity that resembles a gaping toecap that is separated from the sole at the seam. Pitting and sporadic cross-ridging of the nail plate are more common in finger nails than toe nails.[3]
Causes
Its cause is yet unknown. It appears that parakeratosis pustulosa is not inherited if it is not present in siblings or other family members. Psoriasis, onychomycosis, and chronic dry fissured eczematoid dermatitis have all been frequently linked to it.[4]
Diagnosis
The diagnosis of parakeratosis pustulosa is made based on clinical features and the exclusion of other disorders.[4]
Treatment
There is no suggested specific therapy. Topical emollients are still the advised course of treatment, even though topical corticosteroids have been utilized in the majority of reports. Topical tretinoin therapy might not be necessary for many people.[4]
Epidemiology
The exact prevalence of parakeratosis pustulosa is unknown. It is more common in girls and occurs only in children.[4]
See also
References
- ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
- ^ a b Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
- ^ Pandhi, D; Chowdhry, S; Grover, C; Reddy, B S (2003). "Parakeratosis pustulosa - a distinct but less familiar disease". Indian Journal of Dermatology, Venereology and Leprology. 69 (1): 48–50. PMID 17642830. Retrieved 23 March 2024.
- ^ a b c d Mahajan, VikramK; Ranjan, Nitin (2014). "Parakeratosis pustulosa: A diagnostic conundrum". Indian Journal of Paediatric Dermatology. 15 (1). Medknow: 12. doi:10.4103/2319-7250.131828. ISSN 2319-7250.
Further reading
- Tosti, A; Peluso, AM; Zucchelli, V (1998). "Clinical features and long-term follow-up of 20 cases of parakeratosis pustulosa". Pediatric Dermatology. 15 (4). Wiley: 259–263. doi:10.1046/j.1525-1470.1998.1998015259.x (inactive 2024-04-05). ISSN 0736-8046. PMID 9720686.
{{cite journal}}: CS1 maint: DOI inactive as of April 2024 (link) - CRONIN, E.; SAMMAN, P.D. (1986). "Parakeratosis pustulosa". Clinical and Experimental Dermatology. 11 (6). Oxford University Press (OUP): 643–645. doi:10.1111/j.1365-2230.1986.tb00524.x. ISSN 0307-6938. PMID 3665153.
External links
This page was last edited on 8 May 2024, at 20:42