Intravascular Lymphoma with Central Nervous System Involvement: Mayo Clinic Experience
Bryan Neth1, Ugur Sener1, Zafer Keser1, Derek Johnson1, David Abarbanel1, Rafid Mustafa1, Jonas Paludo1, Stephen Ansell1, Robert Brown1, Michel Toledano1
1Mayo Clinic
Objective:

Characterize the disease course, imaging/laboratory features and clinical outcomes of pathologically confirmed intravascular lymphoma with central nervous system (CNS) involvement.

Background:

Intravascular lymphoma is a rare hematologic malignancy, which commonly presents with CNS and skin involvement. There is an incomplete understanding of the typical clinical course, treatment, and outcomes.

Design/Methods:

We retrospectively reviewed our institutional experience of patients with pathologically confirmed intravascular lymphoma (October 1998-November 2019, last review October 2023). Clinical and pathology data were collected from the electronic medical record. Clinical images were reviewed by a neuroradiologist. We performed descriptive statistics. Survival analyses were performed using the Kaplan Meier method.

Results:

We identified 22 patients with CNS involvement of intravascular lymphoma. The median age at diagnosis was 63 years (range: 39-79) with 46% female. Median follow-up was 2.6 years (range: 0.04-17.3). The most common symptoms at presentation were focal neurologic deficit including stroke (73%), constitutional symptoms (59%), cognitive changes (27%), personality changes (18%). Lactate dehydrogenase (LDH) was elevated in most patients (90%, mean 634 units/L). Abnormalities on brain MRI were found in 79% of patients, relative to abnormalities on spine MRI (27%) or angiogram (40%). The most common imaging findings were T2 FLAIR abnormalities (74%), mass-like enhancement (42%), ischemic infarct (26%), meningeal enhancement (26%), and susceptibility weighted changes (5%). CSF cytology was rarely positive for malignancy (6%). The most common first-line therapies were R-CHOP (38%) and R-CHOP+MTX (33%). Median overall survival was 3.8 years (95% CI: 0.8-NA).  

Conclusions:

Patients with CNS involvement of intravascular lymphoma present variably, including with constitutional symptoms and elevated LDH as seen in systemic-only involvement. Abnormalities on brain MRI are common but not necessarily seen. When present, characteristic imaging findings included T2 FLAIR abnormalities and mass-like enhancement. CSF cytology was rarely positive for malignancy. As expected, overall prognosis remains guarded.

10.1212/WNL.0000000000206363