No abstract available.
Purpura ; Purpura, Thrombocytopenic, Idiopathic

No abstract available.
Purpura, Thrombocytopenic, Idiopathic*

No abstract available.
Purpura, Thrombocytopenic, Idiopathic*

No abstract available.
Hemorrhage* ; Purpura, Thrombocytopenic, Idiopathic*

No abstract available.
Purpura, Thrombocytopenic, Idiopathic*

No abstract available.
Dapsone* ; Purpura, Thrombocytopenic, Idiopathic*

Humans ; Purpura, Thrombocytopenic, Idiopathic

Background: Idiopathic or Immune Thrombocytopenic Pupura (ITP) is a common disease in Vietnamese children. This is a hemostatic disorder disease diagnosed by clinical symptoms combining with tests of platelet quantity in peripheral blood and other tests. Objectives: to study epidemiology, clinical, para-clinical characteristics and their relations in ITP disease. Subjects and methods: This was a prospective and retrospective study. The study included 579 pediatric patients from 3 months to 16 ages who were diagnosed and treated ITP disease in National Pediatric Hospital from 1/1/2003 to 12/31/2004. Results: Data were analyzed, including 191 infants from >3-<12 months (33.0%), 293 children from 1 - 10 ages (50.6%), 95 children >10-<16 ages (16.4%). The male/female ratio was highest in infants and decreased with age (P < 0.001). The disease occurred more in September, October and November with advantage factor being acute respiratory infection before 2 to 3 weeks. Subcutaneous hemorrhage ratio was highest with 557 cases (96.2%), intracranial hemorrhage happened in 7 cases (1.7%). There were differences among age groups about hemorrhage situation. Anemia level did not corresponding with the decrease of the platelet count. Conclusion: Characteristics of ITP depend on the number of platelet and age. \r\n', u'\r\n', u'\r\n', u'
Purpura ; Thrombocytopenic ; Idiopathic/ epidemiology

No abstract available.
Methylprednisolone* ; Purpura, Thrombocytopenic, Idiopathic*

A case of Idiopathic Thrombocytopenic Purpura (ITP) in pregnancy managed by multidisciplinary team approach is discussed. A case of 35-year old patient with ecchymoses and easy bruisability at four months age of gestation is presented. Diagnostics revealed prolonged bleeding time with peripheral blood smear and bone marrow aspirate biopsy consistent with ITP. Pertinent findings and evidence on management strategies on ITP in pregnancy were discussed and a consensus was arrived at. The patient was maintained on oral steroids, underwent fetal being surveillance and platelet count monitoring. Patient unremarkably delivered vaginally to a term livebirth who eventually developed neonatal thrombocytopenia. The neonate was treated with steroids and likewise discharged improved.