Yusuf Heba, Kou Aretha, Zelinskas Claire, Ayele Girma, Frunzi Johnathan, Atalay Rediet Tefera, Michael Miriam B
Internal Medicine, HCA Florida Trinity, Trinity, USA.
Internal Medicine, Medical Center of Trinity, Trinity, USA.
Cureus. 2022 Jun 20;14(6):e26112. doi: 10.7759/cureus.26112. eCollection 2022 Jun.
A rare complication of infectious mononucleosis is immune thrombocytopenic purpura (ITP). The majority of people affected by Epstein-Barr Virus (EBV) are below the age of 30, while ITP is usually seen with peaks of incidence in the elderly and children. The unique case of an otherwise healthy 22-year-old female will be discussed, with an initial presentation of ecchymosis, rash, and epistaxis, and was subsequently found to have severe thrombocytopenia. The diagnosis of primary EBV infection due to EBV was eventually made, responsive to intravenous (IV) Methylprednisolone. It is important to consider primary EBV infection in the differential diagnosis of a patient who presents with acute thrombocytopenia.
传染性单核细胞增多症的一种罕见并发症是免疫性血小板减少性紫癜(ITP)。大多数受爱泼斯坦-巴尔病毒(EBV)感染的人年龄在30岁以下,而ITP通常在老年人和儿童中发病率达到高峰。将讨论一名原本健康的22岁女性的独特病例,其最初表现为瘀斑、皮疹和鼻出血,随后被发现患有严重血小板减少症。最终诊断为由EBV引起的原发性EBV感染,对静脉注射甲基强的松龙有反应。在对出现急性血小板减少症的患者进行鉴别诊断时,考虑原发性EBV感染很重要。