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Syndrome in question

descriptionPublicationkeyboard_double_arrow_right Article , Other literature type , Report 01 Apr 2016Publisher:FapUNIFESP (SciELO)Journal:Anais Brasileiros de Dermatologia, volume 91, pages 245-247 (eissn: 0365-0596,

Authors: Rosmaninho, Aristóteles; Carvalho, Sandrina; Oujo, Elena; Horta, Miguel;

doi: 10.1590/abd1806-4841.20164231

pmid: 27192531

pmc: PMC4861579

Syndrome in question

- Summary
- Subjects
- Metrics

Abstract

Neurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (SNF), which corresponds to NF-type 5 in the Riccardi classification, is a rare disorder. It may go unrecognized if few lesions are observed. We present a case of segmental neurofibromatosis in a 28 year-old patient who presented with multiple papules and nodules distributed in dermatomal fashion on the trunk. The histopathological examination of the lesions revealed a non-encapsulated, well-circumscribed spindle cell neoplasm, which was consistent with neurofibromas.

Related Organizations

Centro Hospitalar do Porto
Portugal

Keywords

Adult, Male, Syndrome in Question, Neurofibroma, Skin Neoplasms, Neurofibromatoses, Dermatology, Syndrome, Neurofibromatosis, Rare Diseases, RL1-803, segmentar neurofibromatosis, Humans, Skin

Impact byBIP!

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	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Average
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Average