PURPURA TROMBOCITOPENICA PDF

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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Inflammatory bowel disease and immune thrombocytopenic purpura: Am J Gastroenterol, 92pp. Conclusions In our experience, the most effective treatment for recurrent forms of ITP was intravenous immune globulin, but none of the treatments achieved long-term responses.

We present a case of idiopathic thrombocytopenic purpura in a year-old girl in whom the two diseases first presented simultaneously. Objectives To asses outcome and treatment response purpur patients with chronic or recurrent ITP. Background Immune thrombocytopenic purpura ITP is characterized by a drop in platelet count usually accompanied by hemorrhagic diathesis. Are you a health professional able to prescribe or dispense drugs? Add to My Bibliography. 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.

We use cookies to help provide and enhance our service and tailor content and ads. Tusell Puigbert b S. Immune thrombocytopenic purpura ITP is characterized by a drop in platelet count usually accompanied by hemorrhagic diathesis. Postgrad Med J, 76pp.

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It is particularly rare in association with Crohn’s disease. Gut, 5pp. Trombocitopeniac continuing you agree to the use of cookies. Gastroenterol Hepatol, 26pp.

Se continuar a navegar, consideramos que aceita o seu uso. It is particularly rare in association with Crohn’s disease.

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

In these cases it presents certain peculiarities with respect to its normal clinical features, occurring more frequently when Crohn’s disease is mainly colonic and usually appearing after the diagnosis of Crohn’s disease has been made. Complete resolution of refractory immune thrombocytopenic purpura after colectomy for ulcerative colitis. In our experience, the most effective treatment for trombocitopenjca forms of ITP was intravenous immune globulin, but none of the treatments achieved long-term responses.

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Púrpura trombocitopénica inmune crónica y recurrente – ScienceDirect

Idiopathic thrombocytopenic purpura as an extraintestinal manifestation of crohn’s disease. Haematologica, 83pp. The statiscal analysis was made using descriptive measures. Immune thrombocytopenia and Crohn’s disease.

Disappareance of blocking type thyrotropin binding inhibitors immunoglobuline TBII during thyroid and steroid medication in a patient with autoimmune thyroiditis. A case of Turner’s syndrome with idiopathic thrombocytopenic purpura, and Hashimoto’s thyroiditis detected in the course of ulcerative colitis. Am J Gastroenterol, 91pp. Get Access Get Access. In these cases it presents certain peculiarities with respect to its normal clinical features, occurring more frequently when Crohn’s disease is trombociotpenica colonic and usually appearing after the diagnosis of Crohn’s disease has been made.

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. J Pediatr, 95pp. J Clin Gastroenterol, 32pp. The clinical course was poor and both diseases were refractory to habitual treatment.

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Immune mediated neutropenia and thrombocytopenia in a patient with ulcerative colitis: Further evidence that exacerbation of ulcerative colitis causes the onset of immune thrombocytopenia: J Clin Gastroenterol, 23pp.

National Center for Biotechnology InformationTrombocitopenic. Extraintestinal and systemic manifestations of inflammatory bowel disease. Tormbocitopenica thrombocytopenic purpura in three trombcoitopenica with preexisting ulcerative colitis.

[Clinical analysis of cases of idiopathic thrombocytopenic purpura]. – PubMed – NCBI

Possible causal association between ulcerative colitis and idiopatic thrombocytopenic purpura. Abnormal cellular immune mechanisms associated with autoimmune thrombocytopenia.

Didn’t get the message? Although the number of patients treated with intravenous anti-D immune globulin was low, good results were achieved. Quintana Riera a L. Gastroenterol Clin Biol, 9pp. No significant differences trkmbocitopenica found between the two groups in age, sex, diagnosis, duration of follow-up, previous viral infection, or antiplatelet antibodies.

Key words Chronic immune thrombocytopenic purpura. Clin Lab Hemat, 8pp. A case of primary sclerosing cholangitis associated with ulcerative colitis and idiopathic thrombocytopenic purpura. J Clin Gastroenterol, 18pp. Recommended articles Citing articles 0. Clin Rheumatol, 11pp.

Med Clin North Am, 74pp.