Literature DB >> 22323875

Hereditary sclerosing poikiloderma.

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


  12 in total

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10.  Thrombocytopenia: first symptom in a patient with dyskeratosis congenita.

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