2020
DOI: 10.18203/issn.2455-4529.intjresdermatol20203753
|View full text |Cite
|
Sign up to set email alerts
|

Marginal acrokeratoderma: a case series

Abstract: <p>Marginal acrokeratoderma (MAK) are complex disorders characterized by distribution of cornified papules/plaques along the dorso-plantar and dorso-palmar junction of the feet and hands. They belong to the family of punctate palmoplantar keratoderma. No associated gene defect has been detected. There are two clinically identical types of hereditary/familial MAK; namely acrokeratoelastoidosis (AKE) and focal acral hyperkeratosis (FAH); differentiated by the presence of elastorrehexis in AKE. The aim of t… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2021
2021
2021
2021

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 30 publications
(69 reference statements)
0
1
0
Order By: Relevance
“…Laser therapy, topical corticosteroids, topical and systemic retinoids, cryotherapy, and topical keratolytics are used for its treatment (Bhobe et al 2016). -Differential diagnosis: Different disorders with manifestations of marginal papular keratoderma including hereditary papulotranslucent acrokeratoderma, mosaic acral keratosis, digital popular calcinosis, degenerative collagenous plaques of the hands, and keratoelastoidosis marginalis (Rongioletti et al 1994), and acrokeratosis verruciformis of Hopf, colloid milium, and plane warts (Ibekwe and Ogunbiyi 2020). Acquired keratodermas show different patterns of epidermal involvement including diffuse, focal, and punctate.…”
Section: Marginal Papular Keratodermamentioning
confidence: 99%
“…Laser therapy, topical corticosteroids, topical and systemic retinoids, cryotherapy, and topical keratolytics are used for its treatment (Bhobe et al 2016). -Differential diagnosis: Different disorders with manifestations of marginal papular keratoderma including hereditary papulotranslucent acrokeratoderma, mosaic acral keratosis, digital popular calcinosis, degenerative collagenous plaques of the hands, and keratoelastoidosis marginalis (Rongioletti et al 1994), and acrokeratosis verruciformis of Hopf, colloid milium, and plane warts (Ibekwe and Ogunbiyi 2020). Acquired keratodermas show different patterns of epidermal involvement including diffuse, focal, and punctate.…”
Section: Marginal Papular Keratodermamentioning
confidence: 99%