| Literature DB >> 25093865 |
Susanne Gantner1, Arno Rütten, Luis Requena, Gerhard Gassenmaier, Michael Landthaler, Christian Hafner.
Abstract
CHILD syndrome is an acronym signifying congenital hemidysplasia with ichthyosiform nevus and limb defects. A 27-year-old woman presented with chronic verrucous and hyperkeratotic skin lesions involving the left genital area, left hand and left foot since childhood. The histopathologic findings were consistent with verruciform xanthoma. In correlation with the clinical picture of a linear lesion, the diagnosis of CHILD nevus was made. Subsequent genetic analysis identified a germline c.324C>T (p.A105V) NSDHL mutation and confirmed a diagnosis of CHILD syndrome. This syndrome can be associated with only minimal clinical symptoms. The anatomical distribution of the lesions, a static clinical course and the typical histopathologic features of a CHILD nevus can serve as the clue to a diagnosis of CHILD syndrome in such cases.Entities:
Keywords: CHILD nevus; CHILD syndrome; NSDHL mutation; epidermal nevus; verruciform xanthoma
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Year: 2014 PMID: 25093865 DOI: 10.1111/cup.12377
Source DB: PubMed Journal: J Cutan Pathol ISSN: 0303-6987 Impact factor: 1.587