Literature DB >> 25093865

CHILD syndrome with mild skin lesions: histopathologic clues for the diagnosis.

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.
© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  CHILD nevus; CHILD syndrome; NSDHL mutation; epidermal nevus; verruciform xanthoma

Mesh:

Substances:

Year:  2014        PMID: 25093865     DOI: 10.1111/cup.12377

Source DB:  PubMed          Journal:  J Cutan Pathol        ISSN: 0303-6987            Impact factor:   1.587


  2 in total

Review 1.  Vegas (Verruciform Genital-Associated) Xanthoma: A Comprehensive Literature Review.

Authors:  Katherine M Stiff; Philip R Cohen
Journal:  Dermatol Ther (Heidelb)       Date:  2016-11-15

2.  A novel NSDHL variant in CHILD syndrome with gastrointestinal manifestations and localized skin involvement.

Authors:  Ene-Choo Tan; Shi Yun Chia; Khadijah Rafi'ee; Shan Xian Lee; Andrew Boon Eu Kwek; Sze Hwa Tan; Victor Weng Leong Ng; Heming Wei; Stephanie Koo; Ai Ling Koh; Mark Jean-Aan Koh
Journal:  Mol Genet Genomic Med       Date:  2021-12-26       Impact factor: 2.183

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.