Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s Lines
Lichen striatus (LS) is an uncommon, acquired, self-limited, and benign linear dermatosis of unknown etiology that most often occurs unilaterally and is confined to the lines of Blaschko. A healthy 7-year-old girl presented to our clinic with bilateral asymmetric LS occurring on the right arm and le...
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2018-01-01
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Series: | Case Reports in Dermatological Medicine |
Online Access: | http://dx.doi.org/10.1155/2018/6905175 |
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doaj-c9085129fa6d4dec974ed7a47fc9edcb2020-11-25T02:23:54ZengHindawi LimitedCase Reports in Dermatological Medicine2090-64632090-64712018-01-01201810.1155/2018/69051756905175Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s LinesJeffrey S. Dickman0McKay D. Frandsen1Andrew J. Racette2Midwestern University, Arizona College of Osteopathic Medicine, 19555 N 59th Ave, Glendale, AZ 85308, USAMidwestern University, Arizona College of Osteopathic Medicine, 19555 N 59th Ave, Glendale, AZ 85308, USAOmni Dermatology, Inc., KCU-GMEC Phoenix Dermatology Residency Program, 4840 E Indian School Rd, Suite 102, Phoenix, AZ 85018, USALichen striatus (LS) is an uncommon, acquired, self-limited, and benign linear dermatosis of unknown etiology that most often occurs unilaterally and is confined to the lines of Blaschko. A healthy 7-year-old girl presented to our clinic with bilateral asymmetric LS occurring on the right arm and left leg of 1-year duration. Very few cases of bilateral LS have been previously reported in the literature, with none from clinics within the United States. The etiology of LS is currently unknown; however its confinement to Blaschko’s lines, which represent embryologic migration of skin cell clones, does provide insight into a possible pathogenesis. It seems most likely that an individual’s development of LS is linked to their genetic predisposition and a subsequent triggering event. Our case serves as a strong example of a rare presentation of LS and facilitates discussion of the clinical diagnostic process and possible pathogenesis of this dermatosis.http://dx.doi.org/10.1155/2018/6905175 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jeffrey S. Dickman McKay D. Frandsen Andrew J. Racette |
spellingShingle |
Jeffrey S. Dickman McKay D. Frandsen Andrew J. Racette Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s Lines Case Reports in Dermatological Medicine |
author_facet |
Jeffrey S. Dickman McKay D. Frandsen Andrew J. Racette |
author_sort |
Jeffrey S. Dickman |
title |
Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s Lines |
title_short |
Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s Lines |
title_full |
Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s Lines |
title_fullStr |
Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s Lines |
title_full_unstemmed |
Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s Lines |
title_sort |
asymmetric bilateral lichen striatus: a rare presentation following multiple blaschko’s lines |
publisher |
Hindawi Limited |
series |
Case Reports in Dermatological Medicine |
issn |
2090-6463 2090-6471 |
publishDate |
2018-01-01 |
description |
Lichen striatus (LS) is an uncommon, acquired, self-limited, and benign linear dermatosis of unknown etiology that most often occurs unilaterally and is confined to the lines of Blaschko. A healthy 7-year-old girl presented to our clinic with bilateral asymmetric LS occurring on the right arm and left leg of 1-year duration. Very few cases of bilateral LS have been previously reported in the literature, with none from clinics within the United States. The etiology of LS is currently unknown; however its confinement to Blaschko’s lines, which represent embryologic migration of skin cell clones, does provide insight into a possible pathogenesis. It seems most likely that an individual’s development of LS is linked to their genetic predisposition and a subsequent triggering event. Our case serves as a strong example of a rare presentation of LS and facilitates discussion of the clinical diagnostic process and possible pathogenesis of this dermatosis. |
url |
http://dx.doi.org/10.1155/2018/6905175 |
work_keys_str_mv |
AT jeffreysdickman asymmetricbilaterallichenstriatusararepresentationfollowingmultipleblaschkoslines AT mckaydfrandsen asymmetricbilaterallichenstriatusararepresentationfollowingmultipleblaschkoslines AT andrewjracette asymmetricbilaterallichenstriatusararepresentationfollowingmultipleblaschkoslines |
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1724856496206905344 |