A 65-year-old female with multiple myeloma diagnosed one year before developed tonic-clonic
seizures. She had a good initial response to chemotherapy. Brain magnetic resonance
imaging (MRI; [Figure 1]) and cerebrospinal fluid (CSF; [Figure 2]) analysis showed central nervous system myelomatous infiltration. Intrathecal chemotherapy
and dexamethasone were prescribed and a follow-up CSF sample was negative for plasmocytes.
Neurologic manifestations of multiple myeloma are not uncommon and include spinal
compression and peripheral neuropathy[1]. Central nervous system myelomatosis, on the other hand, is rare. The workup for
the diagnosis includes brain MRI and CSF analysis. CSF cytology has a sensitivity
of 50–60% and a specificity over 95%[2]. Prognosis is poor.
Figure 1 Sagital postcontrast T1-weighted image (1A) shows mixed pachymeningeal and leptomeningeal
thickening forming nodules and intense gadolinium enhancement. Axial T2-weighted image
(1B) and coronal T1-weighted image (1C) show one of these nodules extending into subjacent
brain parenchyma with perilesional edema.
Figure 2 Cerebrospinal fluid specimen with myelomatous cells (arrow). The stain employed was
May-Grunwald-Giemsa. Atypical plasmocytes found in the cerebrospinal fluid were subsequently
confirmed by immunophenotyping.