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1.
J Ayub Med Coll Abbottabad ; 26(2): 203-6, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25603678

RESUMO

BACKGROUND: Psoriasis is a common, chronic, disfiguring, inflammatory and proliferative condition of skin manifested by red, scaly, sharply demarcated, indurated plaques present particularly over the extensor surfaces and scalp. The disease has been found to be associated with celiac disease related antibodies with variable frequencies in different populations of the world. The subset of patients showing this association have a higher psoriasis severity and also respond well to cost effective way of gluten free diet. There is a need to work out the frequency of these antibodies in our local psoriatic patients. METHODS: The study was carried out in Department of Dermatology, Military Hospital Rawalpindi from 4th June to 4th December, 2008. A total of 80 patients of both gender, aged more than 15 with a clinical diagnosis of psoriasis attending dermatology outpatient department were selected. Relevant history and thorough physical examination was performed and disease characteristics like previous treatments received and history of arthropathy were obtained. Coeliac disease related antibodies were assessed on serum by indirect immunofluorescence and data was analysed using software SPSS-13. RESULTS: From the study of 80 patients, celiac disease related antibodies were found in none of the cases. All the severe and mild to moderate patients of psoriasis were negative for IgA antigliadin antibodies, IgG antigliadin antibodies and IgA anti-reticulin antibody. CONCLUSION: This study concludes that celiac disease related antibodies are not present in psoriatic patients irrespective of severity of disease in our local population.


Assuntos
Doença Celíaca/epidemiologia , Doença Celíaca/imunologia , Psoríase/epidemiologia , Adulto , Anticorpos/análise , Estudos Transversais , Feminino , Gliadina/imunologia , Humanos , Imunoglobulina A/imunologia , Masculino , Pessoa de Meia-Idade , Adulto Jovem
2.
J Ayub Med Coll Abbottabad ; 26(4): 633-5, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25672205

RESUMO

We report a case of Langerhan Cell Histiocytosis in a three and a half years old child. The child presented with history of low grade fever, off and on for 9 months. There was 2 months history of progressive pallor and 5 days history of epistaxis. Blood complete picture revealed pancytopenia and the patient was referred to a paediatric oncologist. Initial diagnosis of acute lymphoblastic leukaemia (ALL), Lymphoma and disseminated Tuberculosis (TB) was made on basis of initial investigations. Coetaneous involvement occurred 7 months later along with Diabetes Insipidis, bone changes and pulmonary involvement.


Assuntos
Medula Óssea/patologia , Febre/etiologia , Histiocitose de Células de Langerhans/complicações , Histiocitose de Células de Langerhans/diagnóstico , Antineoplásicos Fitogênicos/uso terapêutico , Biópsia , Pré-Escolar , Epistaxe/etiologia , Histiocitose de Células de Langerhans/tratamento farmacológico , Humanos , Masculino , Pancitopenia/etiologia , Dermatopatias/etiologia , Vimblastina/uso terapêutico
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