Acute Pediatric Immune Thrombocytopenic Purpura with Severe Thrombocytopenia: A Case Report
Asian Hematology Research Journal · pp. 280–284 · Published 25 May 2026
10.9734/ahrj/2026/v9i3254Abstract
Immune thrombocytopenic purpura (ITP) is an acquired autoimmune disorder characterized by isolated thrombocytopenia and an elevated risk of bleeding. It frequently manifests in pediatric patients following viral infections. We present a case of a one-year-old female child who presented with petechial rash and gum bleeding. Laboratory investigations revealed severe thrombocytopenia. The patient was diagnosed with ITP and managed with corticosteroids and supportive care. Early diagnosis and prompt intervention resulted in clinical improvement, underscoring the significance of timely management in pediatric ITP.
Cited by 0
No indexed citations yet.
Related research
Article metrics
Real usage data collected on this platform.
0
Page views
0
PDF downloads
0
Outbound clicks
0
Citations
Views by country
Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".
No views recorded yet.
Traffic sources
Referring site, by host.
No traffic recorded yet.
Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.