TY - JOUR
T1 - An Epstein-Barr virus-positive diffuse large B-cell lymphoma presenting as multi-organ failure: A catastrophic lymphomatosis with fulminant visceral organ dissemination resulting in a precipitous death in a 59-year-old female with no identifiable etiology for immunodeficiency
AU - Wang, E.
AU - Papavassiliou, P.
AU - Wei, Q.
AU - Wickham, M. Q.
AU - Cichon, L.
AU - Proia, Alan
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Epstein–Barr virus (EBV)-positive diffuse large B-cell lymphoma (EBV+ DLBCL) of the elderly is an aggressive B-cell neoplasm related to age-associated impaired immunity . We report such a case in a 59-year-old woman with a catastrophic disease course. The patient initially presented with fever, fatigue, malaise and weakness over one-week period. Despite empirical treatment with antibiotics and antiviral agents, she subsequently developed multi-organ failure and coagulopathy . Radiographic imaging revealed hepatomegaly , splenomegaly , pleural effusion , and ascites . Her complete blood cell count showed marked leukocytosis , anemia and thrombocytopenia. Morphologic examination of blood smear demonstrated many abnormal plasmacytoid lymphocytes , and flow cytometric analysis detected an intermediate-large mature B-cell population (69%) without detectable surface immunoglobulin . High copy numbers of EBV genome were detected in the blood by PCR. A diagnosis of EBV+ DLBCL, leukemic phase, was made. Despite aggressive treatment and supportive care, the patient succumbed to multi-organ failure one week after initial presentation. Autopsy demonstrated EBV+ DLBCL infiltration in all the organs examined. This case describes an unusual presentation of EBV+ DLBCL and highlights the necessity of pertinent ancillary tests to avoid delay in the diagnosis and treatment.
AB - Epstein–Barr virus (EBV)-positive diffuse large B-cell lymphoma (EBV+ DLBCL) of the elderly is an aggressive B-cell neoplasm related to age-associated impaired immunity . We report such a case in a 59-year-old woman with a catastrophic disease course. The patient initially presented with fever, fatigue, malaise and weakness over one-week period. Despite empirical treatment with antibiotics and antiviral agents, she subsequently developed multi-organ failure and coagulopathy . Radiographic imaging revealed hepatomegaly , splenomegaly , pleural effusion , and ascites . Her complete blood cell count showed marked leukocytosis , anemia and thrombocytopenia. Morphologic examination of blood smear demonstrated many abnormal plasmacytoid lymphocytes , and flow cytometric analysis detected an intermediate-large mature B-cell population (69%) without detectable surface immunoglobulin . High copy numbers of EBV genome were detected in the blood by PCR. A diagnosis of EBV+ DLBCL, leukemic phase, was made. Despite aggressive treatment and supportive care, the patient succumbed to multi-organ failure one week after initial presentation. Autopsy demonstrated EBV+ DLBCL infiltration in all the organs examined. This case describes an unusual presentation of EBV+ DLBCL and highlights the necessity of pertinent ancillary tests to avoid delay in the diagnosis and treatment.
UR - https://cufind.campbell.edu/medicine_school/444
UR - https://doi.org/10.1016/j.prp.2013.09.001
U2 - 10.1016/j.prp.2013.09.001
DO - 10.1016/j.prp.2013.09.001
M3 - Article
VL - 210
JO - Pathology - Research and Practice
JF - Pathology - Research and Practice
ER -