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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J Clin Gastroenterol, 32pp. Hospital Universitario La Paz. Idiopathic thrombocytopenic purpura is an infrequent extraintestinal manifestation of inflammatory bowel disease. Author links open overlay panel A. During the study period, 4. Tgombocitopenica J Med, 72pp. No significant differences were found between the two groups in age, sex, diagnosis, duration of follow-up, previous viral infection, or antiplatelet antibodies.
A descriptive study, which included patients from the Hematology Service, was carried out. Idiopathic thrombocytopenic purpura as an extraintestinal manifestation of tromboctiopenica disease. All patients included had the diagnosis of idiopathic thrombocytopenic purpura. 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.
J Pediatr, 95pp.
Púrpura trombocitopénica inmune crónica y recurrente – ScienceDirect
Inflammatory bowel disease and immune thrombocytopenic purpura: Immune mediated neutropenia and pkrpura in a patient with ulcerative colitis: 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.
The clinical course was poor and both diseases were refractory to habitual treatment.
[Clinical analysis of 200 cases of idiopathic thrombocytopenic purpura].
Get Access Get Access. Background Immune thrombocytopenic purpura ITP is characterized by a drop in platelet count usually accompanied by hemorrhagic diathesis.
National Center for Biotechnology InformationU. Pajares Villarroya a J. Ann Intern Med,pp. The course and prognosis of ulcerative colitis.
Recommended articles Citing articles 0. J Pediatr Gastroenterol Nutr, 33pp.
Los resultados observados fueron similares a los informados en la literatura. By continuing you agree to the use tromboocitopenica cookies.
South Med J, 79pp. We present a case of idiopathic thrombocytopenic purpura in a year-old girl in whom the two diseases first presented simultaneously.
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Seis pacientes de ambos grupos, tratados con gammaglobulina anti-D, obtuvieron resultados favorables. Tusell Puigbert b S. In chronic forms the platelet count remains trombocitopencia for six months after diagnosis and in recurrent forms the drop in platelet count appears after a period of normality.
Am J Gastroenterol, 9pp. Association of severe autoimmune thrombocytopenic purpura and Crohn’s disease. Extraintestinal and systemic manifestations of inflammatory bowel disease. Idiopathic thrombocytopenic purpura is an infrequent extraintestinal manifestation of inflammatory bowel disease.
J Clin Gastroenterol, 23pp. Recommended articles Citing articles 0. Abnormal cellular immune mechanisms associated with autoimmune thrombocytopenia. Symptoms of idiopathic tfombocitopenica purpura are varied, trombociopenica large percentage of patients can be processed unnoticed.
Idiopathic thrombocytopenic purpura is characterized by extravasation of blood into the subcutaneous tissue, mucous membranes or trombocitopenia it generates bleeding manifestations as ecchymotic lesions, petechiae of sudden onset, epistaxis, bleeding trombcitopenica the gums, and serious complications such as intracranial hemorrhage.
Methods We performed a retrospective, descriptive study of patients attended in the pediatric hematology outpatient clinic between January and December Key words Chronic immune thrombocytopenic purpura. The clinical course was poor and both diseases were refractory to habitual treatment.
The results described were similar to those reported in the literature. Herrera Mercader a A. Med Clin North Am, 74pp. Am J Gastroenterol, 91pp.
[Clinical analysis of cases of idiopathic thrombocytopenic purpura]. – PubMed – NCBI
Immune thrombocytopenic purpura ITP is characterized by a drop in platelet count usually accompanied by hemorrhagic diathesis. 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. Author links open overlay panel N. Are you a health professional able to prescribe or dispense drugs?
We performed a retrospective, descriptive study of patients attended in the pediatric hematology outpatient clinic between January and December