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爱泼斯坦-巴尔病毒引起的传染性单核细胞增多症中的严重血小板减少症。

Severe thrombocytopenia in Epstein-Barr virus-induced mononucleosis.

作者信息

Steeper T A, Horwitz C A, Moore S B, Henle W, Henle G, Ellis R, Flynn P J

出版信息

West J Med. 1989 Feb;150(2):170-3.

Abstract

Severe thrombocytopenia is a rare complication of Epstein-Barr virus-induced infectious mononucleosis. We evaluated the clinical and laboratory data from seven patients seen between 1976 and 1985 whose lowest platelet counts varied from 3 to 25 x 10(9) per liter. Five of the seven patients were initially thought to have either acute leukemia or idiopathic thrombocytopenic purpura; eventually, however, primary Epstein-Barr virus infections were confirmed in all patients. Two of six patients tested had antiplatelet antibodies during the acute phase of their illnesses. Eight additional patients with acute disease who had only mild thrombocytopenia (94 to 144 x 10(9) per liter) were also tested for platelet antibodies with negative results. Steroid therapy was administered to three patients and platelet transfusions to one. All seven patients recovered with no serious hemorrhagic sequelae.

摘要

严重血小板减少症是爱泼斯坦-巴尔病毒引起的传染性单核细胞增多症的一种罕见并发症。我们评估了1976年至1985年间收治的7例患者的临床和实验室数据,这些患者的最低血小板计数在每升3至25×10⁹之间。7例患者中有5例最初被认为患有急性白血病或特发性血小板减少性紫癜;然而,最终所有患者均确诊为原发性爱泼斯坦-巴尔病毒感染。6例接受检测的患者中有2例在疾病急性期存在抗血小板抗体。另外8例患有急性疾病且仅有轻度血小板减少症(每升94至144×10⁹)的患者也接受了血小板抗体检测,结果为阴性。3例患者接受了类固醇治疗,1例接受了血小板输注。所有7例患者均康复,无严重出血后遗症。

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本文引用的文献

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Platelet-agglutinating factor in glandular fever complicated by jaundice and thrombocytopenia.
Lancet. 1958 Oct 25;2(7052):883-5. doi: 10.1016/s0140-6736(58)92308-0.
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IgM and IgG platelet antibodies in a case of infectious mononucleosis and severe thrombocytopenia.
Scand J Haematol. 1984 Feb;32(2):145-8. doi: 10.1111/j.1600-0609.1984.tb02169.x.

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