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1.
Rev Esp Anestesiol Reanim (Engl Ed) ; 68(2): 114-116, 2021 Feb.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33371977
2.
Actas Dermosifiliogr ; 106(5): 387-401, 2015 Jun.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-25728564

RESUMO

BACKGROUND: Phototherapy is a treatment option for atopic dermatitis recommended by several guidelines. OBJECTIVE: To perform a systematic review of the efficacy of different modalities of phototherapy and photochemotherapy in moderate to severe atopic dermatitis. MATERIAL AND METHODS: We considered all randomized clinical trials (RCTs) performed in patients with atopic dermatitis, and accepted all outcome measures. Articles were identified via an online search of the MEDLINE (via Ovid) and Embase databases and the Cochrane Central Register of Controlled Trials. We also searched for clinical trials registered in Current Controlled Trials and in the World Health Organization's International Clinical Trials Registry Platform. RESULTS: Twenty-one RCTs (961 patients) were included in the qualitative analysis. Two of the trials included children and adolescents (32 patients). The efficacy of narrow-band UV-B and UV-A1 phototherapy was similar for the different outcome measures contemplated. Two RCTs assessed the efficacy of psoralen plus UV-A therapy (PUVA). No serious adverse events were described. In general, the publications reviewed were characterized by a high risk of bias and poor reporting of methodology and results. CONCLUSIONS: There is evidence for the use of narrow-band UV-B and UV-A1 phototherapy in moderate to severe atopic dermatitis. Evidence supporting the use of PUVA in atopic dermatitis is scarce and there is little information on the use of phototherapy in childhood. For the purpose of future studies, it would be advisable to use comparable criteria and scales for the evaluation of disease severity and patients, to standardize radiation methods, and to establish a minimum follow-up time.


Assuntos
Dermatite Atópica/terapia , Fototerapia , Adolescente , Adulto , Criança , Ensaios Clínicos Controlados como Assunto , Dermatite Atópica/tratamento farmacológico , Dermatite Atópica/radioterapia , Humanos , Terapia PUVA , Fototerapia/métodos , Ensaios Clínicos Controlados Aleatórios como Assunto , Resultado do Tratamento , Terapia Ultravioleta
3.
Actas Dermosifiliogr ; 105(4): 359-66, 2014 May.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-23664250

RESUMO

Thiazides are widely used diuretics that first became available in the 1950s. The first reports of photosensitivity reactions to thiazides were published shortly after the introduction of these drugs, but few cases have been described since. We review all the cases of photosensitivity due to thiazides published up to December 2011. We found 62 cases, 33 in women and 29 in men. The most common presentation was eczematous lesions in a photodistributed pattern, and the most common causative agent was hydrochlorothiazide. The results of photobiological studies were published in only some of the cases reviewed. In most cases, phototesting revealed an abnormal response to UV-A alone or to both UV-A and UV-B. In some cases, the results of phototesting were normal and only photopatch testing yielded abnormal results. Diagnosis of photosensitivity due to thiazides requires a high degree of suspicion. Ideally, diagnosis should be confirmed by a photobiological study.


Assuntos
Dermatite Fototóxica/etiologia , Tiazidas/efeitos adversos , Dermatite Fototóxica/diagnóstico , Feminino , Humanos , Masculino
4.
Cytogenet Genome Res ; 138(1): 1-4, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22796746

RESUMO

The presence of a supernumerary 18p isochromosome is a rare chromosomal abnormality that results in 18p tetrasomy. This is a report on the clinical, cytogenetic and molecular findings of 2 non-related patients with a supernumerary 18p isochromosome. Both patients present some features of the 18p tetrasomy syndrome (strabismus, low-set ears, long and narrow fingers and toes), but additional characteristics were also observed. Cytogenetic analysis, FISH, MLPA and SNP array techniques showed that one of the isochromosomes is symmetric and monocentric, while the other is asymmetric and dicentric, yet resulting in a similar tetrasomy of the 18pter-18p10 region, followed by a partial 18q11.2 trisomy, an unprecedented finding in the literature.


Assuntos
Isocromossomos , Trissomia/genética , Criança , Cromossomos Humanos Par 18/genética , Análise Citogenética , Epigênese Genética , Feminino , Humanos , Lactente
5.
Clin Exp Dermatol ; 37(7): 755-8, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22439735

RESUMO

Scleroderma-like cutaneous changes have been reported in association with several drugs, but not with hydroxyurea (HU), to our knowledge. We report the case of a 67-year-old man who was treated with HU (hydroxycarbamide) for 12 years for a myeloproliferative disorder, and presented a progressive pruritic woody induration, symmetrically affecting both legs. He also had Gottron-like papules on the back of the metacarpophalangeal joints, and a retroauricular undifferentiated squamous cell carcinoma. On histological examination of a skin biopsy taken from the leg, massive dermal fibrosis was seen, with thickening of collagen bundles throughout the entire dermis. Six months after HU withdrawal, the skin induration resolved without scarring. Scleroderma-like syndrome has not been previously considered one of the secondary effects of HU. The evolution of our patient's condition supports a causal relationship between the HU treatment and the sclerodermiform changes of the skin.


Assuntos
Antineoplásicos/efeitos adversos , Toxidermias/etiologia , Hidroxiureia/efeitos adversos , Dermatoses da Perna/induzido quimicamente , Esclerodermia Localizada/induzido quimicamente , Idoso , Humanos , Masculino , Resultado do Tratamento
8.
Anal Bioanal Chem ; 402(4): 1481-92, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21904800

RESUMO

Energy dispersive X-ray fluorescence is a common analytical tool for layer thickness measurements in quality control processes in the coating industry, but there are scarce microanalytical applications in order to ascertain semi-quantitative or quantitative information of painted layers. "Oil on copper" painting becomes a suitable material to be analysed by means of X-ray fluorescence spectrometry, due to the metallic nature of substrate and the possibility of applying layered models as used in coating industry. The aim of this work is to study the suitability of a quantitative energy dispersive X-ray fluorescence methodology for the assessment of the areal distribution of pigments and the characterization of painting methods on such kind of pictorial artworks. The method was calibrated using standard reference materials: dried droplets of monoelemental standard solutions laid on a metallic plate of copper. As an example of application, we estimated pigment mass distribution of two "oil on copper" paintings from the sixteenth and eighteenth centuries. Pictorial layers have been complementarily analysed by X-ray diffraction. Apart of the supporting media made of copper or brass, we could identify two different superimposed layers: (a) a preparation layer mainly composed by white lead and (b) the pictorial layer of variable composition depending on the pigments used by the artist on small areas of the painting surface. The areal mass distribution of the different elements identified in the painting pigments (Ca, Cr, Mn, Fe, Zn, Cd, Hg and Pb) have been determined by elemental mapping of some parts of the artworks.

10.
Nucleic Acids Res ; 26(1): 229-3, 1998 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-9399842

RESUMO

The Marfan database is a software that contains routines for the analysis of mutations identified in the FBN1 gene that encodes fibrillin-1. Mutations in this gene are associated not only with Marfan syndrome but also with a spectrum of overlapping disorders. The third version of the Marfan database contains 137 entries. The software has been modified to accommodate four new routines and is now accessible on the World Wide Web at http://www.umd.necker.fr


Assuntos
Bases de Dados Factuais , Síndrome de Marfan/genética , Mutação , Software , Redes de Comunicação de Computadores , Análise Mutacional de DNA , Fibrilina-1 , Fibrilinas , Humanos , Proteínas dos Microfilamentos/genética
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