1.Primary Effusion Lymphoma: An Untrivial Differential Diagnosis for Ascites.
Funda CERAN ; Yusuf AYDIN ; Levent OZCAKAR ; Unsal HAN ; Mehmet YILDIZI
Yonsei Medical Journal 2009;50(6):862-864
A primary effusion lymphoma is a rare type of non-Hodgkin's lymphoma where serous cavities are involved. That-cause peritoneal, pleural and pericardial effusions without any lymphadenopathy. They affect immunosuppressive patients with human herpes virus-8 being the suspected etiological agent. The prognosis is usually poor despite treatment. Herein, the case of an immunocompetent patient with ascites and pleural effusion diagnosed as primary effusion lymphoma is presented and discuss the case in the light of the current literature.
Ascites/*diagnosis
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Fatal Outcome
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Humans
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Lymphoma, Primary Effusion/*diagnosis
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Male
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Middle Aged
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Pleural Effusion/*diagnosis
2.Current Concepts in Primary Effusion Lymphoma and Other Effusion-Based Lymphomas.
Yoonjung KIM ; Chan Jeong PARK ; Jin ROH ; Jooryung HUH
Korean Journal of Pathology 2014;48(2):81-90
Primary effusion lymphoma (PEL) is a human herpes virus 8 (HHV8)-positive large B-cell neoplasm that presents as an effusion with no detectable tumor in individuals with human immunodeficiency virus infection or other immune deficiencies. PEL is an aggressive neoplasm with a poor prognosis. PEL cells show diverse morphologies, ranging from immunoblastic or plasmablastic to anaplastic. The immunophenotype of PEL is distinct, but its lineage can be misdiagnosed if not assessed thoroughly. PEL cells usually express CD45, lack B- and T-cell-associated antigens, and characteristically express lymphocyte activation antigens and plasma cell-associated antigens. Diagnosis of PEL often requires the demonstration of a B-cell genotype. HHV8 must be detected in cells to diagnose PEL. In most cases, PEL cells also harbor the Epstein-Barr virus (EBV) genome. Similar conditions associated with HHV8 but not effusion-based are called "extracavitary PELs." PELs should be differentiated from HHV8-negative, EBV-positive, body cavity-based lymphomas in patients with long-standing chronic inflammation; the latter can occur in tuberculous pleuritis, artificial pneumothorax, chronic liver disease and various other conditions. Despite their morphological similarity, these various lymphomas require different therapeutic strategies and have different prognostic implications. Correct diagnosis is essential to manage and predict the outcome of patients with PEL and related disorders.
B-Lymphocytes
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Diagnosis
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Genome
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Genotype
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Herpesvirus 4, Human
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HIV
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Humans
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Inflammation
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Liver Diseases
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Lymphocyte Activation
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Lymphoma*
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Lymphoma, Primary Effusion*
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Plasma
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Pleurisy
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Pneumothorax, Artificial
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Prognosis