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Pyothorax-associated lymphoma (PAL): a western case with marked angiocentricity and review of the literature.

作者信息

Androulaki A, Drakos E, Hatzianastassiou D, Vgenopoulou S, Gazouli M, Korkolopoulou P, Patsouris E, Dosios T

机构信息

Department of Pathology, Laiko General Hospital, Medical School, University of Athens, Athens, Greece.

出版信息

Histopathology. 2004 Jan;44(1):69-76. doi: 10.1111/j.1365-2559.2004.01737.x.

DOI:10.1111/j.1365-2559.2004.01737.x
PMID:14717672
Abstract

AIMS

To report a case of pyothorax-associated lymphoma in a non-immunocompromised 78-year-old man with a 45-year history of tuberculous pleuritis and left pleural effusion. Pyothorax-associated lymphoma is a high-grade non-Hodgkin's lymphoma occurring in 2% of patients with long-standing tuberculous pleuritis and pyothorax. Pyothorax-associated lymphoma is frequently Epstein-Barr virus (EBV)-associated, mainly reported in Japan but exceedingly rare in western countries.

METHODS AND RESULTS

Histology revealed a high-grade, diffuse large B-cell lymphoma with immunoblastic and plasmacytoid features and marked angiocentricity with focal destruction of the vessel walls. Immunohistochemistry revealed a post germinal B-cell phenotype. RNA in-situ hybridization and molecular analysis showed a latent EBV infection and absence of human herpes virus-8 (HHV-8).

CONCLUSIONS

Pyothorax-associated lymphoma represents a rare but distinctive type of diffuse large B-cell lymphoma, with characteristic clinico-epidemiological, immunohistological, and biological features.

摘要

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