Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 12 de 12
Filtrar
Más filtros












Base de datos
Intervalo de año de publicación
1.
J Cutan Pathol ; 46(12): 898-904, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31373032

RESUMEN

BACKGROUND: Melanocytic acral nevi have a series of distinguishing features, including their location, patient age at onset, clinical progression, and histological findings. In particular, histopathological analysis often reveals a melanocytic acral nevus with intraepidermal ascent of cells (MANIAC nevus), which in some cases can be mistaken for atypia or malignancy. AIM: This study describes the clinicopathological characteristics of acral nevi in patients under 18 years old and contrasts the clinical and histological features between MANIAC vs non-MANIAC nevi. METHODS: This was a retrospective observational study, performed in our department in the decade between January 2007 and January 2017. We included patients younger than 18 years of age who were subjected to the removal of melanocytic acral nevi. RESULTS: A total of 70 patients were studied. 54.2% (38/70) were females and 45.8% (32/70) were males. With regard to the type of nevus, 34 were compound, 27 were junctional, and 9 were predominantly intradermal lesions. We identified a total of 41 MANIAC nevi and 29 non-MANIAC nevi. Statistically significant differences between these two groups were identified in nevus size (larger in MANIAC) and the frequency of compound nevi (higher in the MANIAC group), but not in the remainder of the histological parameters studied.


Asunto(s)
Melanoma/patología , Nevo Intradérmico/patología , Nevo Pigmentado/patología , Nevo/patología , Adolescente , Cuidados Posteriores , Niño , Preescolar , Diagnóstico Diferencial , Femenino , Enfermedades del Pie/patología , Humanos , Masculino , Nevo Pigmentado/epidemiología , Nevo Pigmentado/cirugía , Estudios Retrospectivos , Neoplasias Cutáneas/patología
3.
An Pediatr (Engl Ed) ; 88(6): 309-314, 2018 Jun.
Artículo en Español | MEDLINE | ID: mdl-28838840

RESUMEN

INTRODUCTION: Hand eczema is a frequent disease in adults. Diagnosing the cause of hand eczema is difficult due to different classifications. There is lack of evidence on hand eczema and its causes in children. MATERIAL AND METHOD: A total of 389 children between 0 and 16 years were identified between 1996 and 2016, from whom 42 (10.8%) with exclusively hand eczema were selected. In all cases a standard battery of epicutaneous patch tests was performed, as well as additional batteries depending on the clinical suspicion. The clinical and epidemiological features of these children were recorded and compared against children with eczema in other locations. RESULTS: The 42 children with hand eczema included 25 (60.5%) girls, and 17 (40.5%) boys, with a mean age of 10.6 +- 3.9 years, and did not differ from that of children with eczema in other locations. The definitive diagnosis after patch-testing was Atopic Dermatitis in 15 cases, Allergic Contact Dermatitis in 14 patients, Endogenous Vesiculous Eczema in 6 cases, Endogenous Hyperkeratotic Eczema in 5 cases, and Irritant Contact Dermatitis in 2 cases. The most frequent allergens detected were thiomersal (9 cases), nickel (5 cases), mercury (5 cases), and cobalt (4 cases). CONCLUSION: Hand eczema is a common condition in children. The most common cause is atopic dermatitis, although cases of allergic contact dermatitis manifesting as hand eczema are not uncommon. Any child with eczema of hands in whom an allergic cause is suspected should be referred for patch- testing.


Asunto(s)
Eccema/diagnóstico , Eccema/epidemiología , Dermatosis de la Mano/diagnóstico , Dermatosis de la Mano/epidemiología , Adolescente , Niño , Preescolar , Eccema/inmunología , Estudios Epidemiológicos , Femenino , Dermatosis de la Mano/inmunología , Humanos , Lactante , Masculino , Pruebas del Parche , Prevalencia , Estudios Retrospectivos , Centros de Atención Terciaria
4.
Pediatr Dermatol ; 34(5): 535-539, 2017 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-28730653

RESUMEN

BACKGROUND/OBJECTIVES: Footwear dermatitis is a form of contact dermatitis resulting from exposure to shoes. There have been only small studies regarding foot contact dermatitis in children. The present study was undertaken to define the prevalence and epidemiologic and clinical features of shoe dermatitis in children. METHODS: A retrospective study was undertaken of all children referred for patch testing between 1996 and 2015. Children with dermatitis limited to the feet were selected. RESULTS: We collected data from 389 children younger than 16 years, 52 of whom (13.4%) were referred with dermatitis exclusively on the feet. Diagnosis after patch testing was allergic contact dermatitis in 23 children (44.2%), atopic eczema in 12 (23.1%), juvenile plantar dermatosis in 8 (15.4%), dyshidrotic eczema in 6 (11.5%), irritant contact dermatitis in 2 (3.8%), and tinea pedis in 1 (1.9%). The most frequent allergens were potassium dichromate, thimerosal, cobalt chloride, mercapto mix, colophonium, mercury, and nickel(II) sulfate. CONCLUSION: Allergic contact dermatitis caused by footwear is a common cause of foot dermatitis in children. Children with foot dermatitis should be referred for patch testing when an allergic origin is suspected.


Asunto(s)
Dermatitis Alérgica por Contacto/epidemiología , Dermatosis del Pie/epidemiología , Zapatos/efectos adversos , Adolescente , Alérgenos , Niño , Preescolar , Dermatitis Alérgica por Contacto/etiología , Femenino , Pie , Dermatosis del Pie/diagnóstico , Dermatosis del Pie/etiología , Humanos , Lactante , Masculino , Pruebas del Parche , Prevalencia , Estudios Retrospectivos
6.
Pediatr Dermatol ; 30(6): e230-1, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-22612277

RESUMEN

Microphthalmia with linear skin defects (MLS) or microcornea, dermal aplasia and sclerocornea (MIDAS) syndrome is a rare X-linked-dominant disorder. We present a patient with agenesis of corpus callosum, ocular abnormalities, and multiple skin defects. The cytogenetic studies of the MLS critical region (Xp22.2) were normal, but a skewed X-chromosome inactivation pattern (85:15) was observed.


Asunto(s)
Cromosomas Humanos X , Dermis/patología , Enfermedades Genéticas Ligadas al Cromosoma X/genética , Enfermedades Genéticas Ligadas al Cromosoma X/patología , Microftalmía/genética , Microftalmía/patología , Anomalías Cutáneas/genética , Anomalías Cutáneas/patología , Inactivación del Cromosoma X , Niño , Femenino , Humanos
9.
Am J Dermatopathol ; 34(2): 177-81, 2012 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-22123266

RESUMEN

Intracranial invasion of cellular blue nevus is extremely rare, and its malignant transformation is even less common. The differential diagnosis includes neurocutaneous melanosis and neurocristic cutaneous hamartoma. A 50-year-old female presented with intracranial melanoma in contiguity with a congenital blue nevus on the scalp. The patient showed a wide pigmented lesion on the scalp that had grown in the last few years over the congenital blue nevus. Magnetic resonance imaging revealed an intracranial tumor lying contiguous to the nevus. Despite aggressive surgery, the tumor relapsed and the patient developed systemic metastases. We report a rare case of cellular blue nevus showing an unexpected aggressive behavior with extensive extra- and intracranial expansion and distant metastases.


Asunto(s)
Neoplasias Encefálicas/secundario , Melanoma/secundario , Cuero Cabelludo/patología , Neoplasias Cutáneas/patología , Diagnóstico Diferencial , Femenino , Hamartoma/patología , Humanos , Melanosis/patología , Persona de Mediana Edad , Síndromes Neurocutáneos/patología , Nevo Azul/patología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...