gms | German Medical Science

68th Annual Meeting of the German Society of Neurosurgery (DGNC)
7th Joint Meeting with the British Neurosurgical Society (SBNS)

German Society of Neurosurgery (DGNC)

14 - 17 May 2017, Magdeburg

Intracranial plasmacytomas mimicking meningiomas – two remarkable cases

Meeting Abstract

  • Thomas Fortmann - Klinik für Neurochirurgie, Universitätsklinikum Münster, Münster, Deutschland
  • Benjamin Brokinkel - Klinik für Neurochirurgie, Universitätsklinikum Münster, Münster, Deutschland
  • Walter Stummer - Klinik für Neurochirurgie, Universitätsklinikum Münster, Münster, Deutschland
  • Markus Holling - Klinik für Neurochirurgie, Universitätsklinikum Münster, Münster, Deutschland

Deutsche Gesellschaft für Neurochirurgie. Society of British Neurological Surgeons. 68. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), 7. Joint Meeting mit der Society of British Neurological Surgeons (SBNS). Magdeburg, 14.-17.05.2017. Düsseldorf: German Medical Science GMS Publishing House; 2017. DocP 090

doi: 10.3205/17dgnc653, urn:nbn:de:0183-17dgnc6539

Published: June 9, 2017

© 2017 Fortmann et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.


Outline

Text

Objective: Meningeoma is the most common dural neoplasm. However, a variety of tumor entities may present clinically as meningeoma. Even though a significant number of patients with solitary plasmacytoma, will eventually develop multiple myeloma, intracranial plasmacytoma is exceptional and has been very rarely described as primary manifestation of multiple myeloma.

Methods: Case 1: A 61 year old man presented with a protrusion occipitally on the left side of his head. Cranial MRI showed a lesion suggestive of intraosseous meningioma. Based on typical findings, a neuropathological diagnosis of plasmacytoma was established. This diagnosis prompted complete skeletal radiographs, which revealed an osteolytic lesion of the eighth rib. Bone marrow cytology also revealed neoplastic plasma cells. Case 2: In this 52 year old patient with a progressive occipital mass a MRI supposed a highly vascularized meningioma with compression of the sagittal and transversus sinus. An interventional embolization was conducted preoperatively. Neuropathological examination demonstrated a plasmacytoma.

Results: Intracranial plasmacytomas are rare and infrequently diagnosed by imaging due to their resemblance of meningiomas. On MRI, plasmacytomas are often indistinguishable from meningioma, with intermediate signal on T -weighted sequences and isointense signal to gray matter on proton density and T2-weighted sequences. With contrast, they frequently demonstrate homogenous enhancement, similar to our two cases. The tumors showed the typical histological and immunohistochemical staining profile of plasmacytoma. Since additionally CD20-expressing lymphocytic tumor cells were also encountered in case 1, a diagnosis of “lymphocytic plasmacytoma” was established, which is very rare and may be associated with IgA-heavy chain restriction.

Conclusion: In conclusion, solitary intramedullary plasmacytoma should be considered in the differential diagnosis of meningioma in dural based neoplasms. Vice versa in dural based plasmacytoma lymphocyte rich meningioma must also be considered as a differential diagnosis. In some cases differentiation may be difficult.