León Jorge Esquiche, Takahama Júnior Ademar, Vassallo José, Soares Fernando Augusto, de Almeida Oslei Paes, Lopes Márcio Ajudarte
Departmento de Diagnóstico Oral, Faculdade de Odontologia, Piracicaba Dental School, University of Campinas-UNICAMP, Piracicaba-SP, Brazil.
Int J Surg Pathol. 2011 Apr;19(2):241-6. doi: 10.1177/1066896909353599. Epub 2009 Dec 24.
Posttransplant lymphoproliferative disorders (PTLDs) present a wide clinicopathological spectrum, varying from the usual Epstein-Barr virus (EBV)-driven infectious mononucleosis-type polyclonal proliferations to EBV-positive or EBV-negative proliferations indistinguishable from overt lymphomas that occur in immunocompetent individuals. PTLDs characteristically have a predilection for extranodal sites and association with EBV.These disorders are usually B-cell type, although T-cell and rare cases involving both T- and B-cell types have also been described. The initial treatment consists in decreasing the immnosupressive therapy, usually with favorable results. The authors report on a rare case of a 19-year-old girl, with post-renal transplantation EBV-associated polymorphic lymphoproliferative gingival ulcerated lesions. To the best of their knowledge, this is the first case described in the English-language literature of polymorphic PTLD involving both B-cell and T-cell lineages, with an unusual immunoprofile affecting the mouth. The authors warn that this condition could be easily misdiagnosed as malignant lymphoma if not properly recognized.
移植后淋巴细胞增生性疾病(PTLD)呈现出广泛的临床病理谱,从常见的由爱泼斯坦-巴尔病毒(EBV)驱动的传染性单核细胞增多症样多克隆增生,到与免疫功能正常个体中发生的明显淋巴瘤难以区分的EBV阳性或EBV阴性增生。PTLD的特征是倾向于结外部位并与EBV相关。这些疾病通常为B细胞型,不过也有T细胞型以及罕见的同时涉及T细胞和B细胞型的病例报道。初始治疗包括减少免疫抑制治疗,通常效果良好。作者报告了一例罕见病例,一名19岁女孩,肾移植后出现与EBV相关的多形性淋巴细胞增生性牙龈溃疡病变。据他们所知,这是英文文献中描述的首例涉及B细胞和T细胞谱系的多形性PTLD病例,具有影响口腔的不寻常免疫表型。作者警告说,如果不能正确识别,这种情况很容易被误诊为恶性淋巴瘤。