Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros

Base de dados
País/Região como assunto
Tipo de documento
Intervalo de ano de publicação
1.
Int Wound J ; 14(5): 811-812, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-27910230

RESUMO

A 6-month-old Caucasian baby is described with a postaxial polydactyly of the letf foot. Radiographic examination revealed the accessory digit was composed of soft tissue, some with a tiny osseous element, originated from around the metatarsophalangeal joint, defined by floating type (FT). The parents had consistent difficulty putting shoes. We encountered an exceedingly rare presentation of FT, to our inspection, had neither been previously related in published studies. To the best of our knowledge, this represents the unusual case of congenital deformity lesion on the left foot to be reported in the medical literature.


Assuntos
Anormalidades Congênitas/diagnóstico , Anormalidades Congênitas/cirurgia , Dedos/anormalidades , Articulação Metatarsofalângica/anormalidades , Articulação Metatarsofalângica/fisiopatologia , Polidactilia/diagnóstico , Polidactilia/cirurgia , Dedos do Pé/anormalidades , Feminino , Dedos/cirurgia , Humanos , Lactente , Espanha , Dedos do Pé/cirurgia , Resultado do Tratamento , População Branca
2.
J Tissue Viability ; 25(2): 164-6, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-26944913

RESUMO

A 5-year-old caucasian child is described with a congenital melanocytic periungual and subungual nevus on the right second toe. Histopathologic examination revealed a junctional nevus. Congenital subungual nevi in this location are rare. To the best of our knowledge, this represents the first case of lesion on the right second toe to be reported in the literature.


Assuntos
Doenças do Pé/congênito , Nevo Pigmentado/congênito , Neoplasias Cutâneas/congênito , Pré-Escolar , Feminino , Humanos , Unhas
3.
J Clin Med ; 9(4)2020 Apr 14.
Artigo em Inglês | MEDLINE | ID: mdl-32295260

RESUMO

Subungual osteochondroma (SO) is an infrequent and non-malignant bone tumour of the distal phalanx, especially prominent in paediatric populations. The aim of this research was to describe a case series of paediatric feet with SO which received surgical treatments. The secondary purpose was to compare these descriptive data by sex distribution. METHODS: Twenty-three paediatric feet with SO confirmed by clinical or radiological features received surgical treatment. Socio-demographic (age, sex, height, weight and BMI) and clinical features (side, location, tumour or pain presence, and nail lift before surgery, as well as recurrence and adverse effects at one month after intervention) were reported. RESULTS: Regarding clinical features before intervention, the most frequent locations of SO were the first toe (86.8%) and the right lower limb (56.5%). In addition, the presence of the tumour, pain and nail lift showed a prevalence of 91.3%, 69.5% and 47% of the study sample, respectively. Considering clinical features at one month after intervention, the most frequent adverse effect was the pain presence (69.5%). In addition, one case (4.4%) presented ulceration. Only one patient (4.4%) suffered from recurrence with a new tumour. There were not statistically significant differences by sex distribution (p > 0.05). CONCLUSIONS: This novel study showed that surgery treatment for SO in paediatric populations presented a very low recurrence degree with minor adverse effects and without differences by sex distribution. Thus, further randomized clinical trials should be carried out in order to determine the effectiveness of this intervention in this special population.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA