Intravascular large B-cell lymphoma (IVLBCL) presenting with exclusive cutaneous involvement, no B-symptoms and negative PET-CT: A Case Study.
7 affiliations
- 1Department of Hematology and Oncohematology, Louis Pasteur University Hospital, Faculty of Medicine, Pavol Jozef Šafárik University, Košice, Slovakia.
- 2Department of Radiotherapy and Oncology, East Slovakia Institute of Oncology, Faculty of Medicine, Pavol Jozef Šafárik University, Košice, Slovakia.
- 3Department of Clinical Immunology and Allergology, Louis Pasteur University Hospital and OKIA s.r.o, Košice, Slovakia.
- 4Department of Pathology, Louis Pasteur University Hospital, Košice, Slovakia.
- 5Department of Pharmacology, Faculty of Medicine, Pavol Jozef Šafárik University, Košice, Slovakia.
- 6Faculty of Medicine, Pavol Jozef Šafárik University and OKIA s.r.o, Košice, Slovakia.
- 7Department of Cardiology, Kardiocentrum AGEL-Šaca a.s., Faculty of Medicine, Pavol Jozef Šafárik University, Košice, Slovakia.
Abstract
Intravascular large B-cell lymphoma (IVLBCL) is a rare and aggressive subtype of extranodal non-Hodgkin lymphoma (NHL) that typically involves the central nervous system (CNS) and skin in its classic (Western) variant and frequently presents with systemic B-symptoms. We present a rare case of IVLBCL in a 59-year-old female with cutaneous-only involvement, no B-symptoms, and negative PET-CT. The patient's initial presentation mimicked inflammatory conditions, contributing to diagnostic delay. Deep skin biopsy was crucial and confirmed the diagnosis of IVLBCL. PET-CT was non-revealing, showing limitations in cutaneous-dominant disease. The patient underwent R-CHOP treatment along with CNS prophylaxis, achieving complete remission with no relapse at follow-up. This case emphasizes the importance of high suspicion and early biopsy in atypical cutaneous presentations and the need for personalized strategies.
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BibTeX
@article{gabzdilova2026intravascular,
title = {{Intravascular large B-cell lymphoma (IVLBCL) presenting with exclusive cutaneous involvement, no B-symptoms and negative PET-CT: A Case Study.}},
author = {Juliana Gabzdilova and Atila David Homolya and Stefan Raffac and Frantisek Gmitter and Tomas Guman and Viktoria Hazikova and Martina Maria Raffacova and Filip Breznen},
journal = {Leukemia research reports},
year = {2026},
month = oct,
doi = {10.1016/j.lrr.2026.100619},
url = {https://europepmc.org/article/MED/42959444},
note = {CC BY},
}
RIS
TY - JOUR
TI - Intravascular large B-cell lymphoma (IVLBCL) presenting with exclusive cutaneous involvement, no B-symptoms and negative PET-CT: A Case Study.
AU - Juliana Gabzdilova
AU - Atila David Homolya
AU - Stefan Raffac
AU - Frantisek Gmitter
AU - Tomas Guman
AU - Viktoria Hazikova
AU - Martina Maria Raffacova
AU - Filip Breznen
PY - 2026
DA - 2026/10/17
JO - Leukemia research reports
DO - 10.1016/j.lrr.2026.100619
UR - https://europepmc.org/article/MED/42959444
AB - Intravascular large B-cell lymphoma (IVLBCL) is a rare and aggressive subtype of extranodal non-Hodgkin lymphoma (NHL) that typically involves the central nervous system (CNS) and skin in its classic (Western) variant and frequently presents with systemic B-symptoms. We present a rare case of IVLBCL in a 59-year-old female with cutaneous-only involvement, no B-symptoms, and negative PET-CT. The patient's initial presentation mimicked inflammatory conditions, contributing to diagnostic delay. Deep skin biopsy was crucial and confirmed the diagnosis of IVLBCL. PET-CT was non-revealing, showing limitations in cutaneous-dominant disease. The patient underwent R-CHOP treatment along with CNS prophylaxis, achieving complete remission with no relapse at follow-up. This case emphasizes the importance of high suspicion and early biopsy in atypical cutaneous presentations and the need for personalized strategies.
SN - 2213-0489
ER -