EBV-Associated Polymorphic Posttransplant Lymphoproliferative Disorder Presenting as Gingival Ulcers

Author:

Esquiche León Jorge1,Takahama Júnior Ademar2,Vassallo José3,Soares Fernando Augusto4,Paes de Almeida Oslei2,Ajudarte Lopes Márcio2

Affiliation:

1. Piracicaba Dental School, University of Campinas-Unicamp, Av Limeira 901, Caixa Postal 52, 13414-903, Piracicaba-SP, Brazil,

2. Piracicaba Dental School, University of Campinas-Unicamp, Av Limeira 901, Caixa Postal 52, 13414-903, Piracicaba-SP, Brazil

3. CIPED, State University of Campinas Medical School, Rua Tessália Viera de Camargo, 126, Campinas-SP, 13083-970, Brazil

4. Hospital AC Camargo. Rua Prof Antônio Prudente, 109-1°andar Anatomia Patológica Liberdade, São Paulo-SP, Brazil

Abstract

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.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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