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Intraparenchymal low-grade B-cell lymphomas of the central nervous system: Clinicopathologic and molecular analysis of three cases and a review of the literature.
Dawid de Vera, Maria Teresa; Díaz Crespo, Francisco Javier; Manso, Rebeca; Penedo Coello, Agustín; Morillo-Giles, Daniel; Rodríguez-Pinilla, Socorro María; Díaz de la Pinta, Francisco Javier.
Affiliation
  • Dawid de Vera MT; Pathology Department, Institute of Biomedical Research in Malaga (IBIMA-Plataforma BIONAND), Virgen de la Victoria University Hospital, University of Málaga, 29010 Málaga, Spain. Electronic address: tdawiddevera@gmail.com.
  • Díaz Crespo FJ; Pathology Department, University General Hospital Gregorio Marañón, 28007 Madrid, Spain.
  • Manso R; Pathology Department, Institute of Biomedical Research Fundación Jiménez Díaz, University Hospital Fundación Jiménez Díaz, 28040 Madrid, Spain.
  • Penedo Coello A; START Madrid-CIOCC Phase I Unit, University Hospital HM Sanchinarro, 28050 Madrid, Spain.
  • Morillo-Giles D; Hematology Department, University Hospital Fundación Jiménez Díaz, 28040 Madrid, Spain.
  • Rodríguez-Pinilla SM; Pathology Department, Institute of Biomedical Research Fundación Jiménez Díaz, University Hospital Fundación Jiménez Díaz, 28040 Madrid, Spain; Medicine Department, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
  • Díaz de la Pinta FJ; Pathology Department, Institute of Biomedical Research Fundación Jiménez Díaz, University Hospital Fundación Jiménez Díaz, 28040 Madrid, Spain.
Ann Diagn Pathol ; 73: 152376, 2024 Sep 19.
Article in En | MEDLINE | ID: mdl-39321755
ABSTRACT
Primary central nervous system (CNS) lymphomas represent 1 % of all non-Hodgkin lymphomas, with diffuse large B-cell lymphomas as the prevailing subtype. Low-grade B-cell lymphomas are exceptional with only 24 marginal zone B-cell lymphomas (EMZL) and 1 follicular lymphoma (FL) previously reported so far. While their molecular profiles are studied elsewhere, data on primary intraparenchymal CNS cases remain limited. The objective of the present study is to contribute new cases of primary intraprenchymal low-grade B-cell lymphomas in the CNS and characterize their mutational profile. We conducted a comprehensive review of cases and a literature review to identify similar instances. Clinical, imaging, histological, immunohistochemical, and molecular characteristics were analyzed. Diagnoses were established according to established criteria. We present three novel cases of intraparenchymal CNS low-grade B-cell lymphomas. One case of intraparenchymal EMZL exhibited plasmacytic differentiation, while another lacked a plasma cell component. The third case was diagnosed as FL. The L265P mutation of MYD88 was absent in all cases. Next generation sequencing revealed pathogenic mutations in SPEN (Glu1970ValfsTer64) and ARID1A (Pro1355LeufsTer118) genes in one EMZL case. In conclusion, intraparenchymal CNS low-grade B-cell lymphomas are rare, with few reported cases. Our findings expand knowledge on their clinical and molecular features. We present the first molecular profile of primary CNS intraparenchymal EMZL, underscoring the need for further research to understand their biology and optimize treatment strategies.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Diagn Pathol Journal subject: PATOLOGIA Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Diagn Pathol Journal subject: PATOLOGIA Year: 2024 Document type: Article Country of publication: United States