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青少年传染性单核细胞增多症

Infectious mononucleosis in adolescents.

作者信息

Chetham M M, Roberts K B

机构信息

Department of Pediatrics, University of Massachusetts Medical Center, Worcester.

出版信息

Pediatr Ann. 1991 Apr;20(4):206-13. doi: 10.3928/0090-4481-19910401-10.

Abstract

Infectious mononucleosis is a clinical manifestation of primary EBV infection in adolescents, characterized by a triad of clinical, laboratory, and serologic features. The classic signs and symptoms are not seen in every patient; rather, the presentations tend to fit into one of three clinical forms (pharyngeal, glandular, or febrile). Recognizing these syndromes provides a useful framework for anticipating the clinical course, complications, and differential diagnosis. Nonclassic presentations of IM include a wide variety of neurologic abnormalities, thrombocytopenic purpura, and splenic rupture. The laboratory features of IM include absolute lymphocytosis with a large percentage of atypical lymphocytes, and abnormal liver chemistries in 90% of patients. The diagnosis of IM is confirmed serologically, usually with the demonstration of heterophile antibodies; the test can conveniently be performed in office laboratories. If the heterophile antibody test is negative, EBV-specific serologic tests can identify whether the illness is due to primary EBV infection. Once the diagnosis of IM is made, appropriate guidelines for resumption of activity should be provided to patients, especially to those with evidence of splenomegaly. Medical management includes supportive therapy with adequate analgesia. Corticosteroids are indicated for patients with upper airway obstruction; they may be helpful in patients with neurologic, hematologic, or cardiac complications. Acyclovir may prove to be useful, but further studies are needed before its use can be recommended.

摘要

传染性单核细胞增多症是青少年原发性EB病毒感染的一种临床表现,其特征为临床、实验室及血清学三联征。并非每位患者都会出现典型的体征和症状;相反,其表现往往符合三种临床类型(咽型、腺型或发热型)之一。认识这些综合征为预测临床病程、并发症及鉴别诊断提供了一个有用的框架。传染性单核细胞增多症的非典型表现包括多种神经学异常、血小板减少性紫癜及脾破裂。传染性单核细胞增多症的实验室特征包括绝对淋巴细胞增多且有很大比例的异型淋巴细胞,以及90%的患者肝功能异常。传染性单核细胞增多症的诊断通过血清学检查确诊,通常是检测嗜异性抗体;该检测可在门诊实验室方便地进行。如果嗜异性抗体检测为阴性,EB病毒特异性血清学检测可确定疾病是否由原发性EB病毒感染所致。一旦确诊传染性单核细胞增多症,应向患者提供恢复活动的适当指导方针,尤其是对那些有脾肿大证据的患者。医疗管理包括给予充分镇痛的支持性治疗。对于有上呼吸道梗阻的患者应使用皮质类固醇;它们可能对有神经学、血液学或心脏并发症的患者有帮助。阿昔洛韦可能有用,但在推荐使用之前还需要进一步研究。

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