Clinicopathological features of fibrin-associated diffuse large B-cell lymphoma: a report of six cases.
10.3760/cma.j.cn112151-20230128-00075
- VernacularTitle:纤维素相关大B细胞淋巴瘤6例临床病理特征观察
- Author:
Lan SUN
1
;
Peng LI
2
;
Xiao Ge ZHOU
1
;
Xiao Jing TENG
1
;
Yuan Yuan ZHENG
1
;
Yan Lin ZHANG
1
;
Jian Lan XIE
1
Author Information
1. Department of Pathology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
2. Department of Pathology, First Affiliated Hospital, Wenzhou Medical University, Wenzhou 325000, China.
- Publication Type:Journal Article
- MeSH:
Humans;
Male;
Middle Aged;
Atrial Fibrillation;
Epstein-Barr Virus Infections;
Fibrin/genetics*;
Herpesvirus 4, Human/genetics*;
In Situ Hybridization, Fluorescence;
Lymphoma, Large B-Cell, Diffuse/pathology*;
Myxoma;
Proto-Oncogene Proteins c-bcl-2/genetics*;
Proto-Oncogene Proteins c-bcl-6/genetics*
- From:
Chinese Journal of Pathology
2023;52(6):592-598
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the clinical, pathological and immunophenotypic features, molecular biology and prognosis of fibrin-associated large B-cell lymphoma (LBCL-FA) in various sites. Methods: Six cases of LBCL-FA diagnosed from April 2016 to November 2021 at the Beijing Friendship Hospital, Capital Medical University, Beijing, China and the First Affiliated Hospital, Wenzhou Medical University, Wenzhou, China were collected. The cases were divided into atrial myxoma and cyst-related groups. Clinical characteristics, pathological morphology, immunophenotype, Epstein Barr virus infection status, B-cell gene rearrangement and fluorescence in situ hybridization of MYC, bcl-2, bcl-6 were summarized. Results: The patients' mean age was 60 years. All of them were male. Three cases occurred in atrial myxoma background, while the others were in cyst-related background, including adrenal gland, abdominal cavity and subdura. All cases showed tumor cells located in pink fibrin clot. However, three cyst-related cases showed the cyst wall with obviously fibrosis and inflammatory cells. All cases tested were non germinal center B cell origin, positive for PD-L1, EBER and EBNA2, and were negative for MYC, bcl-2 and bcl-6 rearrangements, except one case with MYC, bcl-2 and bcl-6 amplification. All of the 5 cases showed monoclonal rearrangement of the Ig gene using PCR based analysis. The patients had detailed follow-ups of 9-120 months, were treated surgically without radiotherapy or chemotherapy, and had long-term disease-free survivals. Conclusions: LBCL-FA is a group of rare diseases occurring in various sites, with predilection in the context of atrial myxoma and cyst-related lesions. Cyst-related lesions with obvious chronic inflammatory background show more scarcity of lymphoid cells and obvious degeneration, which are easy to be missed or misdiagnosed. LBCL-FA overall has a good prognosis with the potential for cure by surgery alone and postoperative chemotherapy may not be necessary.
