TY - JOUR
T1 - Guttate leukoderma and acrokeratosis verruciformis of Hopf
T2 - A rare combination in Darier disease
AU - Sun, Christina W.
AU - Grossman, Shoshana K.
AU - Valdes-Rodriguez, Rodrigo
AU - Lee, Jason B.
AU - Hsu, Sylvia
N1 - Publisher Copyright:
© 2020 Dermatology Online Journal. All rights reserved.
PY - 2020/1
Y1 - 2020/1
N2 - A distinct Darier phenotype presenting with confetti-like hypopigmented macules was first described in 1965. Designated as “guttate leukoderma,” this skin finding is a rarely-reported presentation of Darier disease. It has been theorized that the mutation in ATP2A2 causes defective Ecadherin, which in turn disrupts the adhesion of melanocytes to keratinocytes, thus leading to impaired dendrite formation, hindered melanin transfer, and ultimately to melanocyte apoptosis. Herein, we contribute a case of a 56-year old woman who presented with the rarely-described guttate leukoderma of Darier disease and acrokeratosis verruciformis of Hopf.
AB - A distinct Darier phenotype presenting with confetti-like hypopigmented macules was first described in 1965. Designated as “guttate leukoderma,” this skin finding is a rarely-reported presentation of Darier disease. It has been theorized that the mutation in ATP2A2 causes defective Ecadherin, which in turn disrupts the adhesion of melanocytes to keratinocytes, thus leading to impaired dendrite formation, hindered melanin transfer, and ultimately to melanocyte apoptosis. Herein, we contribute a case of a 56-year old woman who presented with the rarely-described guttate leukoderma of Darier disease and acrokeratosis verruciformis of Hopf.
KW - Acrokeratosis verruciformis of Hopf
KW - Calcium
KW - Darier disease
KW - Genodermatosis
KW - Guttate leukoderma
UR - http://www.scopus.com/inward/record.url?scp=85081934954&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85081934954&partnerID=8YFLogxK
M3 - Article
C2 - 32155025
AN - SCOPUS:85081934954
SN - 1087-2108
VL - 26
JO - Dermatology online journal
JF - Dermatology online journal
IS - 1
M1 - 6
ER -