Volume 49, Issue 2 pp. 232-240
ORIGINAL ARTICLE

The cytopathological spectrum of lymphomas in effusions in a tertiary center in Taiwan

Ren Ching Wang MD

Ren Ching Wang MD

Department of Pathology and Laboratory Medicine, Taichung Veterans General Hospital, Taichung, Taiwan

Department of Nursing, College of Nursing, HungKuang University, Taichung, Taiwan

Search for more papers by this author
Yi-Hsiao Chen MS

Yi-Hsiao Chen MS

Department of Pathology and Laboratory Medicine, Taichung Veterans General Hospital, Taichung, Taiwan

Search for more papers by this author
Bo-Jung Chen MD

Bo-Jung Chen MD

Department of Pathology, Shuang-Ho Hospital, Taipei Medical University, New Taipei City, Taiwan

Search for more papers by this author
Shih-Sung Chuang MD

Corresponding Author

Shih-Sung Chuang MD

Department of Pathology, Chi-Mei Medical Center, Tainan, Taiwan

Department of Pathology, School of Medicine, National Taiwan University, Taipei, Taiwan

Correspondence

Prof. Shih-Sung Chuang MD, Department of Pathology, Chi-Mei Medical Center, 901 Chung-Hwa Road, Yong-Kang District, Tainan 71004, TAIWAN.

Email: [email protected]

Search for more papers by this author
First published: 25 September 2020
Citations: 2

Background

Lymphomas presenting in effusions could either be primary or secondary, with very limited data from Taiwan.

Methods

We retrospectively reviewed effusion lymphomas from our archives in a tertiary center from July 2011 to June 2019.

Results

We identified 59 specimens from 43 patients, including 7 cases with primary effusion lymphoma (PEL) and 36, secondary effusion involvement. Half of the secondary cases presented concurrently with effusion lymphoma, while the remaining half-experienced effusion lymphoma during disease progression. All patients with PELs were males with a median age of 77 and presented with massive pleural effusion. None was HIV-related. Two (29%) PEL cases were positive for human herpes virus 8 (HHV8). The only case with plasmablastic phenotype in the PEL group was positive for both HHV8 and EBV. Four patients died shortly after diagnosis; while the remaining three were alive at the last follow-up (two at 13 months and one at 99 months). Of the secondary cases, diffuse large B-cell lymphoma/high grade B-cell lymphoma was the most common (n = 16, 44%), followed by mantle cell lymphoma (n = 5, 14%). Only 8 cases (22%) were T-cell neoplasms. Prognosis for patients with secondary effusion involvement was dismal, with 1- and 2-year overall survival rates at 17% and 8%, respectively.

Conclusion

We found a wide cytopathological spectrum of effusion lymphoma in Taiwan. Most of our PEL cases were distinct from that defined in the World Health Organization scheme by a B-cell phenotype, HHV8-negativity, and absence of immunodeficiency. As compared to PEL cases, the prognosis of those with secondary involvement was extremely poor.

CONFLICT OF INTEREST

The authors declare no potential conflict of interest.

DATA AVAILABILITY STATEMENT

Data available on request from the authors.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.