Background Collet–Sicard’s syndrome is a rare manifestation of skull base disease involving
the jugular and hypoglossal foramina. We report the first case of Collet–Sicard’s
syndrome attributable to extramedullary plasmacytoma-multiple myeloma (EP-MM), which
is also the second case of EP-MM and the sixth case of any plasma cell neoplasm precipitating
a jugular foramen syndrome (JFS)-spectrum disorder.
Methods Case report and literature review.
Results A 59-year-old woman presented with 4 months of left aural fullness and pulsatile
tenderness, positional vertigo, hoarseness, and dysphagia. Examination identified
left tongue weakness and nonspecific sensory abnormalities of the left ear, pharynx,
and throat localizing to cranial nerves IX to XI. Imaging revealed a 3.4 × 1.4 × 2.8
cm lytic lesion extending from the left jugular foramen into the posterior fossa,
for which she was referred to neurosurgery for consideration of resection. A second,
much smaller (1.1 cm) lytic lesion in the left posterior occipital bone was incidentally
discovered by the surgeon during the preoperative consultation. A stereotactic biopsy
of the occipital lesion was subsequently recommended, which identified plasma cell
neoplasm. Serum studies and skeletal survey were consistent with MM, and definitive
pathologic diagnosis of MM with cranial EP was confirmed via bone marrow biopsy.
Conclusion Tumors of the jugular foramen present with a diverse array of lower cranial nerve
deficits, including Collet–Sicard’s syndrome, a rare subset of JFS-spectrum diseases.
Paragangliomas are the most common jugular foramen neoplasms, followed by schwannomas;
however, many other rare entities have been reported as masqueraders, and diligent
work-up with consideration for preliminary biopsy is recommended, particularly in
the presence of additional lesions, equivocal imaging findings, or highly suspicious
cases.
