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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Objectives To asses outcome and treatment response in patients with chronic or recurrent ITP. Inflammatory bowel disease associated with immune thrombocytopenic purpura in children. Hemorrhagic rectocolitis associated with idiopatic thrombocytopenic purpura.

We present a case of idiopathic thrombocytopenic purpura in a year-old girl in whom the two diseases first presented simultaneously.

Are you a health professional able to prescribe or dispense drugs? J Clin Gastroenterol, 32pp. Immune thrombocytopenia and ulcerative colitis. Crohn’s colitis and idiopathic thrombocytopenic purpura.

Abnormal cellular immune mechanisms associated with autoimmune thrombocytopenia. Although the number of patients treated with intravenous anti-D immune globulin was low, good results were achieved. Ann Intern Med,pp.

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Púrpura trombocitopénica inmune crónica y recurrente – ScienceDirect

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. Trombociitopenica Clin Gastroenterol, 18pp. Key words Chronic immune thrombocytopenic purpura. Hospital Universitario La Paz. Erdozain Sosa a R.

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

A case of primary sclerosing cholangitis associated with ulcerative colitis and idiopathic thrombocytopenic purpura. Gastroenterol Clin Biol, 9pp. Idiopathic thrombocytopenic purpura is characterized by extravasation of blood into the subcutaneous tissue, mucous membranes or skin; it generates bleeding manifestations as ecchymotic lesions, petechiae of sudden onset, epistaxis, bleeding from the gums, and serious complications such as intracranial hemorrhage.

This condition is due to a platelet destruction mediated by antibodies directed against the surface of the platelets. J Pediatr, 95pp. Nippon Shokakibyo Gakkai Zasshi, 91pp. Am J Gastroenterol, 92pp. Gastroenterol Hepatol, 26pp. By continuing you agree to the use of cookies. 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 trombocitkpenica of Crohn’s disease has been made.


Author links open overlay panel N. Clin Rheumatol, 11pp. Disappareance of blocking type thyrotropin binding inhibitors immunoglobuline TBII during trombocitopenicca and steroid medication in a patient with autoimmune thyroiditis.

Idiopathic thrombocytopenic purpura is an infrequent extraintestinal manifestation of inflammatory bowel disease. Haematologica, 83pp.

Pajares Villarroya a J. Los resultados observados fueron similares a los informados en la literatura. Med Clin North Am, trombocltopenicapp.

Idiopathic thrombocytopenic purpura is an infrequent extraintestinal trombocitopenoca of inflammatory bowel disease. Background Immune thrombocytopenic purpura ITP is characterized by a drop in platelet count usually accompanied by hemorrhagic diathesis.

Get Access Get Access. It is particularly rare in association with Crohn’s disease. Immune thrombocytopenia and ulcerative colitis: Am J Gastroenterol, 9pp. Methods We performed a retrospective, descriptive study of patients attended in the pediatric hematology outpatient clinic between January and December Add to My Bibliography.