CASE STUDY: IMMUNE THROMBOCYTOPENIA PURPURA IN 6-YEAR OLD FEMALE CHILD
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Keywords
Immune Thrombocytopenic Purpura, ITP, Pediatric Hematology, Case Presentation, Diagnosis, Treatment, Complications.
Abstract
Background: The goal is to offer a comprehensive examination of the patient's clinical appearance, diagnostic evaluation, therapy, results, and any related complications.
Methods: A 6-year-old female child presented with a large whitening, purplish bruise on her left flank. The past medical history included neonatal jaundice, full immunization, and normal developmental milestones. Physical examination revealed purpura on the left flank, without hepatosplenomegaly or lymphadenopathy. The patient's vital signs were stable.
Management: The patient received initial treatment with IV Immunoglobulin (IVIG) and IV steroids. Subsequent treatment included oral steroids, leading to complications such as rubella and facial puffiness.
Conclusion: The conclusion highlighted the complexity and variability of ITP in children, emphasizing the necessity of interdisciplinary care, patient education, and continuous monitoring for achieving optimal outcomes.
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Dr Shafa Sarwar
Whipps Cross University Hospital London