Objective: Primary effusion lymphoma (PEL) is a rare non-Hodgkin lymphoma (NHL) subtype caused by Kaposi sarcoma (KS) herpesvirus. We describe PEL incidence and survival in people with HIV (PWH) and people without HIV in the US.
Design: Retrospective cohort study of PEL people with and without HIV.
Methods: PEL cases were identified in the HIV/AIDS Cancer Match (HACM) Study, a linkage of population-based cancer and HIV registries in 14 US regions. PEL incidence was examined using negative binomial regression and compared with the general population using a standardized incidence ratio. Survival was evaluated using Cox proportional hazard regression.
Results: During 2001-2019, 53% of 174 PEL cases identified in HACM data were among PWH. PWH had >700-fold higher PEL incidence than the general population. Compared to PEL cases without HIV, PWH were younger (median age: 44.8 vs. 77.7 years). Among PWH, prior KS was associated with 59-fold higher PEL incidence versus those without an AIDS diagnosis. PEL comprised 1.15% of the 8010 NHLs diagnosed among PWH in HACM during 2001-2019. HIV was not associated with mortality among PEL cases. Among PWH, Burkitt lymphoma and diffuse large B-cell lymphoma exhibited similar mortality to PEL but central nervous system lymphoma mortality was worse.
Conclusions: There are two distinct subgroups of PEL cases in the US: younger patients with HIV and older patients without HIV. The proportion of PEL cases among PWH is highly disproportionate to the size of the HIV population, reflecting the greatly elevated incidence of PEL among PWH.
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http://dx.doi.org/10.1097/QAD.0000000000004154 | DOI Listing |
Virchows Arch
March 2025
Pathology Department, Instituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD, UAM), Avd. Reyes Católicos 2, Madrid, 28040, Spain.
The 5th edition of the World Health Organization (WHO) and the International Consensus Classification (ICC 2022) recently recognized a subtype of diffuse large B cell lymphoma (DLBCL), respectively called fluid overload-associated large B-cell lymphoma (FO-LBCL) and human herpes virus 8 (HHV8)/Epstein-Barr (EBV)-negative primary effusion-based lymphoma. However, few reports have provided a molecular profile for this entity. We present two cases, both females, who presented to our hospital with, respectively, massive pleural and pericardial effusion, but with no other significant pathological findings, and for both of whom FO-LBCL was the final diagnosis.
View Article and Find Full Text PDFUnlabelled: Colorectal cancer (CRC) has increased at an alarming rate amongst younger (< 50 years) individuals. Such early-onset colorectal cancer (EOCRC) has been particularly notable within the Hispanic/Latino population. Yet, this population has not been sufficiently profiled in terms of two critical elements of CRC -- the MYC proto-oncogene and WNT signaling pathway.
View Article and Find Full Text PDFTicks Tick Borne Dis
February 2025
Department of Animal Biosciences (HBIO), Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden. Electronic address:
Ixodes ricinus, the most common tick species in Northern Europe, plays a significant role as a vector of several pathogens, with its geographical distribution expanding in recent years. In Southern Sweden, particularly in Region Skåne County (referred to as Skåne), the favorable climate and landscape conditions support extensive proliferation of I. ricinus.
View Article and Find Full Text PDFAIDS
February 2025
Division of Cancer Epidemiology & Genetics, National Cancer Institute.
Objective: Primary effusion lymphoma (PEL) is a rare non-Hodgkin lymphoma (NHL) subtype caused by Kaposi sarcoma (KS) herpesvirus. We describe PEL incidence and survival in people with HIV (PWH) and people without HIV in the US.
Design: Retrospective cohort study of PEL people with and without HIV.
J Med Cases
February 2025
Department of Pathology and Laboratory Medicine, Harbor-UCLA Medical Center, Torrance, CA 90502, USA.
Primary effusion lymphoma (PEL) is a rare, aggressive large B-cell lymphoma variant that is invariably associated with human herpesvirus 8 (HHV8), predominantly in human immunodeficiency virus (HIV)-infected patients, and its oncogenicity is often augmented by coinfection with Epstein-Barr virus. It typically presents as a serous effusion in body cavities without detectable solid tumors. The extracavitary variant of PEL may represent a diagnostic challenge.
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