2012
DOI: 10.3346/jkms.2012.27.2.225
|View full text |Cite
|
Sign up to set email alerts
|

Hereditary Sclerosing Poikiloderma

Abstract: Hereditary sclerosing poikiloderma (HSP) is a very rare disease. The clinical features are principally widespread poikiloderma and linear hyperkeratotic and sclerotic bands. We report an 18-yr-old male who presented reticular hyperpigmented lesions on the trunk and extremities since 2-yr-old. Also, linear sclerosing bands appeared on both antecubital and popliteal fossae after yr. Histopathologic finding showed dense sclerotic collagen fibers with telangiectasia in the upper dermis and fragmentations of damage… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
5
0

Year Published

2014
2014
2021
2021

Publication Types

Select...
5
1
1

Relationship

0
7

Authors

Journals

citations
Cited by 7 publications
(5 citation statements)
references
References 10 publications
0
5
0
Order By: Relevance
“…Acrogeria manifests at the time of birth or shortly afterwards with poikiloderma limited to acral parts 3 . Hereditary sclerosing poikiloderma presents in childhood with generalized poikiloderma with accentuation in flexures and extensor surfaces along with sclerodermatous plaques on palms and soles 4 . Dyskeratosis congenita is characterized by triad of severe nail involvement, poikiloderma conspicuous over neck and leucoplakia at a later age 5 .…”
Section: Discussionmentioning
confidence: 99%
“…Acrogeria manifests at the time of birth or shortly afterwards with poikiloderma limited to acral parts 3 . Hereditary sclerosing poikiloderma presents in childhood with generalized poikiloderma with accentuation in flexures and extensor surfaces along with sclerodermatous plaques on palms and soles 4 . Dyskeratosis congenita is characterized by triad of severe nail involvement, poikiloderma conspicuous over neck and leucoplakia at a later age 5 .…”
Section: Discussionmentioning
confidence: 99%
“… 3 Hereditary sclerosing poikiloderma presents in childhood with generalized poikiloderma with accentuation in flexures and extensor surfaces along with sclerodermatous plaques on palms and soles. 4 Dyskeratosis congenita is characterized by the triad of severe nail involvement, poikiloderma conspicuous over the neck, and leucoplakia at a later age. 5 Kindler syndrome is characterized by poikiloderma that develops at the age of 2 to 3 years in photo‐exposed sites along with acral blisters and mucosal stenosis.…”
Section: Discussionmentioning
confidence: 99%
“…Acrogeria manifests at the time of birth or shortly afterward with poikiloderma limited to acral parts 3 . Hereditary sclerosing poikiloderma presents in childhood with generalized poikiloderma with accentuation in flexures and extensor surfaces along with sclerodermatous plaques on palms and soles 4 . Dyskeratosis congenita is characterized by the triad of severe nail involvement, poikiloderma conspicuous over the neck, and leucoplakia at a later age 5 .…”
Section: Discussionmentioning
confidence: 99%
“…Men reportedly are more severely affected. 20 To date, published case reports of HSP are scarce, and the underlying gene defect remains to be elucidated.…”
Section: Dyskeratosis Congenitamentioning
confidence: 99%
“…20 Histopathological features of the sclerotic lines are compatible with scleroderma, showing fibrosis in the reticular dermis, with small and hyalinized sweat glands. Calcinosis is observed in subcutaneous tissue as well as in the aortic valve, where it causes microstenosis and regurgitation.…”
mentioning
confidence: 94%