Multiple myeloma case reports

A case report describes a 67-year-old woman who had received adoptive immunotherapy with chimeric antigen receptor T cells for multiple myeloma and was experiencing parkinsonism-like symptoms 1).


Bilateral Orbital Lesions Presenting as the First Manifestation of Multiple Myeloma 2)

A 77-year-old woman was transferred from the dementia clinic in July 2012. She had a large heterogeneous signal mass with central necrosis and with pial involvement in the left frontal lobe with destruction of the frontal bone that was observed on computed tomography and magnetic resonance imaging. Multiple punched out radiolucent lesions were also noted on the skull X-ray. Serum protein electrophoresis revealed an IgA-kappa monoclonal gammopathy. External lumbar drainage was helpful for treating the fluid collection underneath the scalp after an orbitozygomatic craniotomy with duroplasty 3).

1993

A case of IgD myeloma who developed a glioblastoma multiforme in the left temporal lobe after a partial remission is reported. The clinical and laboratory particular features of IgD myeloma are pointed out and the association of the multiple myeloma and secondary neoplasms is discussed 4).

1992

A case of Ig-G k-type multiple myeloma with metastasis to the left frontal lobe extending to the right basal ganglia without involvement of the cranium. A 71-year-old male complained of exertional dyspnea and lumbago. His laboratory data revealed hyperproteinemia and an abnormal increase in Ig-G (6117mg/dl) in his serum. Serum protein immunoelectrophoresis revealed an IgG k-type band, and Bence-Jones protein was detected in his urine. MMPP, VMCP, VIPP and MP chemotherapy was given, and serum IgG level decreased to a normal range. 21 months after his first admission, incontinence, disorientation, gait disturbance and apathy developed. CT-scan showed an isodense lesion with massive edema in the left frontal lobe and right basal ganglia. On MRI, a Gd-DTPA enhancing lesion was detected extending from the left frontal to the opposite frontal lobe through the splenium. No abnormal skull punched out lesions were noted. Left frontal lobectomy was performed. Histopathology revealed plasmablastic myeloma cells with clear nucleole and eccentric nucleus in the cerebrum. He was diagnosed as having intracerebral metastasis of multiple myeloma without involvement of the cranium. Unfortunately, he died of pancytopenia and pneumonia. The case suggests the possibility of metastasis via blood into the cerebrum 5).

1986

A case of multiple myeloma is reported showing intracranial hypertension due to a large tumor that developed in the left parietal bone. There are only 13 case reports about cranial mass lesion of multiple myeloma since 1928. A 52 year-old female was admitted to Iwate Prefectural Isawa Hospital suffering from headache, nausea and vomiting. She had been already diagnosed as multiple myeloma and treated with chemotherapy using Cyclophosphamide, Melphalan and Prednisolone for 2 years. On admission, a large subcutaneous mass was presented on the left parietal region. Craniogram revealed large osteolytic lesion of the left parietal bone and 3 punched-out lesions of the frontal bone. CT scan revealed a large mass lesion in the left epidural space, diploe and subcutaneous space. Angiography showed avascular area. Brain scintigram showed diffuse hot area. Other skeletal bones showed no abnormality. Laboratory examination revealed high concentration of gamma-globulin and high erythrocyte sedimentation rate. Electrophoresis showed high value of immunoglobulin G; immunoglobulin assay was as follows: IgG-6000 mg/dl, IgA-150 mg/dl, IgM-410 mg/dl, IgE-0 mg/dl. Serum electrolytes were within normal limits. Urine didn't include Bence-Jones protein. The patient was diagnosed as multiple myeloma suffering from intracranial hypertension caused by large tumor which developed in the left parietal bone. On the operation, large tumor was existed in the epidural and subcutaneous space invading into the diploe but without infiltration into the dura mater or cerebral cortex 6).


POLYCYTHEMIA AND QUADRIPLEGIA IN MULTIPLE MYELOMA 7)


1)
Gudera JA, Baehring JM, Karschnia P. Parkinsonism Following Chimeric Antigen Receptor T Cell Therapy. JAMA Neurol. 2024 Aug 12. doi: 10.1001/jamaneurol.2024.2506. Epub ahead of print. PMID: 39133506.
2)
Tripathi M, Syal S, Satarkar R, Gandhoke CS. Bilateral Orbital Lesions Presenting as the First Manifestation of Multiple Myeloma. Neurol India. 2024 May 1;72(3):690-691. doi: 10.4103/neurol-india.Neurol-India-D-24-00225. Epub 2024 Jun 30. PMID: 39042013.
3)
Yi HJ, Hwang HS, Moon SM, Shin IY, Choi YH. A case of multiple myeloma with brain parenchyme involvement. Brain Tumor Res Treat. 2013 Oct;1(2):103-6. doi: 10.14791/btrt.2013.1.2.103. Epub 2013 Oct 31. PubMed PMID: 24904901; PubMed Central PMCID: PMC4027111.
4)
González Silva M. [Second neoplasm in a patient diagnosed with IgD myeloma. Presentation of a case and review of the literature]. Sangre (Barc). 1993 Feb;38(1):47-9. Review. Spanish. PubMed PMID: 8385807.
5)
Harada K, Yoshida J, Wakabayashi T, Sugita K, Ichihara M, Hotta T, Nagamatsu M. [A case of multiple myeloma with intracerebral metastasis]. No Shinkei Geka. 1992 Oct;20(10):1113-7. Japanese. PubMed PMID: 1407349.
6)
Sugita K, Kayama T, Ohwada K, Ichinose M, Takasugi R, Ishizaki T. [A case of multiple myeloma showing intracranial hypertension due to large cranial mass lesions]. No To Shinkei. 1986 Jul;38(7):625-9. Japanese. PubMed PMID: 3756028.
7)
HILL GC. POLYCYTHEMIA AND QUADRIPLEGIA IN MULTIPLE MYELOMA. A CASE REPORT. Ohio State Med J. 1963 Oct;59:1005-8. PMID: 14051020.
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