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1.
Ann Pathol ; 34(4): 339-43, 2014 Aug.
Artigo em Francês | MEDLINE | ID: mdl-25132446

RESUMO

Systemic EBV+ T-cell lymphoproliferative disease of childhood is a recent entity described in the 2008 World Health Organisation tumours of haematopoietic system and lymphoid tissues as a clonal T-cell EBV+ systemic proliferation. It occurs after acute or chronic active EBV infection. We report the case of a caucasian, immunocompetent 12-year-old girl, with no particular history, who presented with hemophagocytic lymphohistiocytosis in the aftermath of an infectious mononucleosis. Main symptoms were multiple organ failure, hepatosplenomegaly and pancytopenia. Histopathology of peripheral lymph node and bone marrow revealed a T-cell, CD8+, EBV+ lymphoproliferation. An elevated viral load was detected in blood by PCR. The patient died within 3 weeks. Since most of the cases have been reported in Asia and South America, few cases still have been described in Europe. Unlike B-cell lymphoproliferation in immunocompromised individuals, T-cell EBV+ lymphoproliferation occurs in immunocompetent patients and seems to be the consequence of a proliferative disorder of EBV-infected T-cells, attributed to a cytotoxic T-cell response deficiency. These T-cell proliferations are more frequently immunoreactive for CD8 than CD4. A key feature of the diagnosis might be EBV viral load.


Assuntos
Linfócitos T CD8-Positivos/patologia , Infecções por Vírus Epstein-Barr/patologia , Transtornos Linfoproliferativos/patologia , Viremia/patologia , Medula Óssea/patologia , Medula Óssea/virologia , Linfócitos T CD8-Positivos/virologia , Criança , Células Clonais/patologia , Células Clonais/virologia , DNA Viral/sangue , Infecções por Vírus Epstein-Barr/diagnóstico , Evolução Fatal , Feminino , Humanos , Imunocompetência , Mononucleose Infecciosa/complicações , Linfonodos/patologia , Linfonodos/virologia , Linfo-Histiocitose Hemofagocítica/etiologia , Transtornos Linfoproliferativos/diagnóstico , Transtornos Linfoproliferativos/virologia , Insuficiência de Múltiplos Órgãos/etiologia , Reação em Cadeia da Polimerase , Carga Viral , Viremia/diagnóstico
2.
Case Rep Oncol ; 8(1): 164-8, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25873885

RESUMO

Breast metastasis from other primary carcinoma is very rare and could be difficult to identify despite immunohistochemistry analysis. Breast metastasis from lung adenocarcinoma can mimic triple-negative breast cancer. Given the prognosis and therapeutic challenges, a correct diagnosis appears essential, and molecular biomarkers could be useful. We report the case of a 52-year-old woman with a breast mass initially diagnosed as primary breast cancer and secondarily attached to breast metastasis from an EGFR-mutated lung adenocarcinoma. The same activating EGFR mutations were identified in both the primary lung carcinoma and the breast metastasis.

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