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Difference between revisions of "Immune thrombocytopenic purpura"
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{{ Infobox diagnosis | |||
| Name = {{PAGENAME}} | |||
| Image = | |||
| Width = | |||
| Caption = | |||
| Synonyms = immune thrombocytopenia | |||
| Micro = germinal centres in white pulp (~55% of cases), [[neutrophil]]s in the red pulp (~67% of cases), macrophages in the red pulp | |||
| Subtypes = clinical: primary, secondary | |||
| LMDDx = | |||
| Stains = | |||
| IHC = | |||
| EM = | |||
| Molecular = | |||
| IF = | |||
| Gross = +/-prominent white nodules (spleen), normal appearance (most common) | |||
| Grossing = | |||
| Site = systemic - see ''[[spleen]]'' | |||
| Assdx = | |||
| Syndromes = | |||
| Clinicalhx = | |||
| Signs = | |||
| Symptoms = bleeding | |||
| Prevalence = uncommon | |||
| Bloodwork = thrombocytopenia, antiplatelet antibodies | |||
| Rads = | |||
| Endoscopy = | |||
| Prognosis = dependent on underlying cause | |||
| Other = | |||
| ClinDDx = | |||
| Tx = corticosteroids, possibly splenectomy | |||
}} | |||
'''Immune thrombocytopenic purpura''', abbreviated '''ITP''', is a rare condition. | '''Immune thrombocytopenic purpura''', abbreviated '''ITP''', is a rare condition. | ||