Maxillary Swelling as the First Evidence of Multiple Myeloma

Multiple myeloma is a malignant neoplasm of plasma cells characterized by proliferation of a single clone of abnormal immunoglobulin-secreting plasma cells. Since the amount of hemopoietic bone marrow is decreased in the maxilla, oral manifestations of multiple myeloma are less common in the maxilla than in the mandible. We report the case of 33-year-old Japanese man who presented with a mass in the right maxillary alveolar region. Computed tomography and magnetic resonance images showed a soft tissue mass in the right maxilla eroding the anterior and lateral walls of the maxillary sinus and extending into the buccal space. The biopsy results, imaging, and laboratory investigations led to the diagnosis of multiple myeloma. This case report suggests that oral surgeons and dentists should properly address oral manifestations as first indications of multiple myeloma.


Introduction
Multiple myeloma, a malignant neoplasm of plasma cells, is the most common primary bone malignancy characterized by monoclonal proliferation of plasma cells [1,2]. The diagnosis of multiple myeloma usually is confirmed by abnormal immunoglobulin (M-protein) in the serum or urine and/or multiple punched-out radiolucent lesions together with histologic confirmation of malignant growth of plasma cells [3]. The clinical manifestations of the disease occur due to an expanding mass of plasma cells in the bone marrow [4]. The most common clinical signs and symptoms of multiple myeloma include renal failure, bone pain, fatigue, anemia, hypercalcemia, and infectious diseases [4,5].
Oral manifestations of multiple myeloma very rarely present as the initial signs [6]. Few case reports of multiple myeloma with maxillary involvement have been published. We describe a case of multiple myeloma involving the maxilla in a 33-year-old man who experienced swelling with mobility of the teeth in the right maxillary alveolar region.

Case Report
A 33-year-old Japanese man presented with diffuse swelling in the right cheek and maxillary alveolar region with mobility of the adjacent teeth, the first premolar and first and second molars ( Figure 1). The upper left second premolar had been extracted 10 years previously due to dental root fracture. A soft, nonpulsatile, nontender, and nonhemorrhagic intraoral mass extended from the right first premolar to the tuberosity region. A panoramic radiograph showed an ill-defined osteolytic lesion in the right posterior maxilla with resorption of the floor of the maxillary sinus ( Figure 2). An axial section computed tomography (CT) image showed a soft tissue density mass measuring 45 × 35 mm in the right maxilla eroding  plus dexamethasone chemotherapy in the hospital and has tolerated the chemotherapy well until now.

Discussion
Multiple myeloma accounts for 1% of all malignancies and slightly more than 10% of hematologic malignancies [5]. The diagnosis of multiple myeloma depends on the identification of abnormal monoclonal plasma cells and the results of a full blood count, bone marrow biopsy, M-protein levels in the serum or urine, and clinical images consistent with multiple myeloma [7]. Bone marrow examination showed a large amount of these abnormal plasma cells, which produce Mprotein light chain proteins ( and types), and cytokines. In the current case, serum protein electrophoresis showed an IgG monoclonal spike of 2.33 g/dL with the and light chains. Excessive production of M-protein causes serum hyperviscosity, which in turn leads to renal dysfunction [8,9]. Although urine electrophoresis may identify M-protein in 60% of patients [ urine. Myeloma cells are typically positive for CD138 [2], which is a useful molecule for determining the extent of plasma cellular infiltration that expresses immunoglobulin in the cytoplasm and occasionally on the cellular surface. Therefore, immunohistochemistry is critical to confirm multiple myeloma [12].
Multiple, well-defined, punched-out radiolucencies without a definitive cortical margin that often contain abnormal plasma cellular proliferations are radiographic features of multiple myeloma [13]. 18 F-FDG PET/CT scans can visualize focal alterations of the bone marrow before punched-out radiolucencies are detected by conventional radiographs [14]. Whereas the current case did not have punched-out radiolucent lesions, 18 F-FDG PET/CT showed multiple strong SUVs in the right maxillary sinus, right submandibular region, and left pubic bone, indicating that 18 F-FDG PET/CT is a helpful tool for diagnosing multiple myeloma. Treatment of multiple myeloma involves mainly irradiation, chemotherapy, and autologous stem cell transplantation. Prognosis is determined via risk classification by the International Staging System (ISS), which defines three risk categories using serum concentrations of 2 microglobulin and albumin [2,15]. In the current case, because both concentrations were low, the current case was classified as ISS stage I with a median survival period of 62 months. Our patient underwent bortezomib plus dexamethasone chemotherapy and has tolerated the chemotherapy well until now.
Oral manifestations of multiple myeloma rarely present as the first signs [13,14,[16][17][18]; the clinical features are swelling, orofacial pain, mobility of teeth, paresthesia, hemorrhage, fracture, and root resorption [13,19]. The maxilla and mandible are the more common regions at which multiple myeloma occurs, with incidence rates ranging from 8% to 15% among the regions of oral manifestations [20]. Since maxillary swelling and mobility of the maxillary molars were the first signs in the current case, carcinoma of the maxillary sinus and metastatic carcinoma from other organs should be considered in the differential diagnosis.
In summary, we reported a rare case of multiple myeloma presenting with swelling in the maxilla as a first sign and suggest that oral surgeons and dentists should properly address oral manifestations as first indications of multiple myeloma.

Consent
The patient provided written informed consent.

Disclosure
All the authors have seen and agreed to submit the report.

Conflict of Interests
The authors declare that there is no conflict of interests regarding publication of this report.