2018
DOI: 10.1111/tid.13005
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Primary effusion lymphoma of the pleural space: Report of a rare complication of cardiac transplant with review of the literature

Abstract: Primary effusion lymphoma (PEL) is a rare mature B‐cell non‐Hodgkin’s lymphoma arising in body cavities and presenting with effusions. It has been described predominantly in patients with impaired immunity from the acquired immunodeficiency syndrome and is associated with the Human Herpesvirus‐8 (HHV‐8). Seldom has PEL been diagnosed in persons negative for the human immunodeficiency virus (HIV), and in such cases it has occurred primarily in the setting of posttransplant immunosuppression. We report an instru… Show more

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Cited by 14 publications
(33 citation statements)
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“…Ever since its first report in patients with advanced HIV infection , PEL has been subsequently diagnosed in HIV‐uninfected patients. Many of these HIV‐uninfected cases were identified in HHV‐8‐endemic regions, or were found in recipients of organ transplantation undergoing immunosuppressive therapy . Sporadic cases have been reported in patients with neither HIV infection nor transplantation history from other regions including Japan and South Korea .…”
Section: Discussionmentioning
confidence: 99%
“…Ever since its first report in patients with advanced HIV infection , PEL has been subsequently diagnosed in HIV‐uninfected patients. Many of these HIV‐uninfected cases were identified in HHV‐8‐endemic regions, or were found in recipients of organ transplantation undergoing immunosuppressive therapy . Sporadic cases have been reported in patients with neither HIV infection nor transplantation history from other regions including Japan and South Korea .…”
Section: Discussionmentioning
confidence: 99%
“…In 2/4 cases, KS preceded PEL, developing 5 months after transplant [2,4] and in one of these, KS initially progressed despite chemotherapy and reduction of immunosuppressive treatment (mycophenolate mofetil stopping and tacrolimus plus prednisone reduction); then KS partial remission was obtained with rapamycin administration and tacrolimus stopping [4]. In 1/4 cases, KS was discovered at post-mortem examination [11], whereas in 1/4 cases, KS occurred before transplant and was successfully treated with radiotherapy, but it recurred at PEL diagnosis [12]. In the case reported by Christenson, the patient developed squamous cell carcinoma of head and neck and was treated with surgery plus chemotherapy and radiotherapy [9].…”
Section: Malignancies Other Than Pelmentioning
confidence: 99%
“…In 1/13 cases, only antiviral treatment with cidofovir was used [4]. Changes in the immunosuppressive treatment were performed at PEL diagnosis in 4/13 cases as follows: 1/4: tacrolimus was changed to sirolimus (rapamycin) resulting in undetectable HHV8 DNA blood level [12]; 1/4: cyclosporine reduction [2]; 1/4: cyclosporine reduction plus azathioprine stopping [3]; 1/4: cyclosporine and azathioprine stopping plus introduction of rapamycin [5]. In 1/13 cases, tacrolimus was changed to rapamycin due to altered renal function, 1 month prior PEL diagnosis and then rapamycin was continued [9].…”
Section: Treatment and Outcomementioning
confidence: 99%
“…Common clinical manifestations of MCD include fevers, pancytopenia, lymphadenopathy, elevated inflammatory markers and splenomegaly [136]. The diagnosis of PEL should be considered in a patient presenting with effusions in relation to serosal surfaces of the body (pericardium, pleural, peritoneal) [137,138]. Concomitant occurrence of multiple disease manifestations of HHV-8 has also been reported in transplant recipients including KS and MCD [139][140][141], and KS, MCD and HLH [142].…”
Section: Clinical Manifestations Of Hhv-8: Oncogenic and Non-oncogenimentioning
confidence: 99%