5 Abr Gac Méd Méx Vol No. 5, Resumen. La púrpura trombocitopénica autoinmune (PTA) es un síndrome causado por la destrucción. Púrpura trombocitopénica y bartonelosis aguda en Huaraz, Perú. 6. Acta Med Per. 23(1) INTRODUCCIÓN. La bartonelosis humana o enfermedad de. Resumen. La púrpura trombocitopénica idiopática es una manifestación extraintestinal poco frecuente de la enfermedad inflamatoria intestinal, y sobre todo es.

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Idiopathic thrombocytopenic purpura with Crohn’s disease.

Immune thrombocytopenia and ulcerative colitis. Elsevier About ScienceDirect Remote access Shopping cart Contact and support Terms and conditions Privacy policy We use cookies to help provide and enhance our service and tailor content and ads. We use cookies to help provide and enhance our service and tailor content and ads. Good results were obtained in six patients from both groups treated with intravenous anti-D immune globulin. Hemorrhagic rectocolitis associated with idiopatic thrombocytopenic purpura.

Can J Gastroenterol, 9pp. Continuing navigation will be considered as acceptance of this use. Postgrad Med J, 76pp. Generate a file for use with external citation management software. Immune thrombocytopenic purpura, neutropenia and sclerosing cholangitis associated with ulcerative colitis in an adult. Quintana Riera a L. Background Immune thrombocytopenic purpura ITP is characterized by a drop in platelet count usually accompanied by hemorrhagic diathesis.


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[Clinical analysis of 200 cases of idiopathic thrombocytopenic purpura].

We performed a retrospective, descriptive study of patients attended in the pediatric hematology outpatient clinic between January and December Can colectomy cure immune thrombocytopenic purpura in a patient with ulcerative colitis?.

Herrera Mercader a A. In chronic forms the platelet count remains low for six months after diagnosis and in recurrent forms the drop in platelet count appears after a trombocitopenicq of normality. During the study period, 4. By continuing you agree to the use of cookies. Immune thrombocytopenia and Crohn’s disease.

You can change the settings or obtain more information by clicking here. Moreover, it usually complicates the clinical course of both diseases.

Erdozain Sosa a R. Endocrinol Jpn, 34pp.

Idiopathic thrombocytopenic purpura is an infrequent extraintestinal manifestation of inflammatory bowel disease. This condition is due to a platelet destruction mediated by antibodies directed uprpura the surface of the platelets.

Transfus Med Rev, 9pp. A descriptive study, which included patients from the Hematology Service, was carried out. Si continua navegando, consideramos rtombocitopenica acepta su uso. Seis pacientes de ambos grupos, tratados con gammaglobulina anti-D, obtuvieron resultados favorables. Immune thrombocytopenic purpura ITP is characterized by a drop in platelet count usually accompanied by hemorrhagic diathesis. It is particularly rare in association with Crohn’s disease.


Further evidence that exacerbation of ulcerative colitis causes the onset of immune thrombocytopenia: Didn’t get the message? Immune thrombocytopenia and ulcerative colitis: Recommended articles Citing articles 0. We present a case of idiopathic thrombocytopenic purpura in a year-old girl in whom the two diseases first presented simultaneously.

Púrpura trombocitopénica inmune crónica y recurrente – ScienceDirect

Abnormal cellular immune purpur associated with autoimmune purpra. Am J Gastroenterol, 9pp. Med Clin North Am, 74pp. In chronic forms, splenectomy is an effective alternative when the risk of hemorrhage is high, while a watchful attitude seems to be the best option when this risk is absent.

A case of Turner’s syndrome with idiopathic thrombocytopenic purpura, and Hashimoto’s thyroiditis detected in the course of ulcerative colitis. The statiscal analysis was made using descriptive measures.