| Literature DB >> 22323875 |
Hyo Jin Lee1, Dong Hoon Shin, Jong Soo Choi, Ki Hong Kim.
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 damaged elastic fibers in the elastic stain, consistent with HSP. We report the first Korean case of HSP.Entities:
Keywords: Hereditary Sclerosing Poikiloderma; Korean
Mesh:
Year: 2012 PMID: 22323875 PMCID: PMC3271301 DOI: 10.3346/jkms.2012.27.2.225
Source DB: PubMed Journal: J Korean Med Sci ISSN: 1011-8934 Impact factor: 2.153