@Article{Sobjanek2014,
journal="Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii",
issn="1642-395X",
volume="31",
number="6",
year="2014",
title="Case reportSegmental neurofibromatosis",
abstract="Segmental neurofibromatosis or type V neurofibromatosis is a rare genodermatosis characterized by neurofibromas, café-au-lait spots and neurofibromas limited to a circumscribed body region. The disease may be associated with systemic involvement and malignancies. The disorder has not been reported yet in the Polish medical literature. A 63-year-old Caucasian woman presented with a 20-year history of multiple, flesh colored, dome-shaped, soft to firm nodules situated in the right lumbar region. A histopathologic evaluation of three excised tumors revealed neurofibromas. No neurological and ophthalmologic symptoms of neurofibromatosis were diagnosed.",
author="Sobjanek, Michał
and Dobosz-Kawałko, Magdalena
and Michajłowski, Igor
and Pęksa, Rafał
and Nowicki, Roman",
pages="410--412",
doi="10.5114/pdia.2014.40942",
url="http://dx.doi.org/10.5114/pdia.2014.40942"
}