Abstract

Purpose: To report a retro-orbital localization of Multiple Myeloma (MM) describing its treatment and clinical result. Case report: A 50-years-old male patient with Magnetic Resonance Imaging (MRI) evidence of a retro-orbital mass with exophthalmos, due to the pathological diagnosis of MM, was referred for Radiation Therapy (RT). Discussion: The orbital involvement in Multiple Myeloma is rare and few cases are reported in the literature. The treatment of choice is RT alone with a prescribed dose ranging between 40 Gy and 45 Gy. In our patient the retro-orbital lesion, measuring 26 × 16 mm, was treated with Intensity Modulated Radiotherapy Technique (IMRT) delivering 4400 cGy with conventional fractionation. The treatment was well tolerated, the patient experienced a complete regression of the exophthalmos without any significant side effect.

Highlights

  • The orbital involvement in Multiple Myeloma is rare and few cases are reported in the literature

  • Multiple Myeloma (MM) is a monoclonal proliferation of plasma cell that causes destructive skeletal lesions and secondary systemic effects, and is a systemic disease diagnosed in the presence of light chain (Bence Jones) proteinuria, lytic skeletal lesions, and characteristic pathology

  • We report the case of a 50-year-old man who presented right exophthalmos with Magnetic Resonance (MRI) evidence of a retro-orbital mass and with a clinical and pathological history of MM

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Summary

Introduction

Multiple Myeloma (MM) is a monoclonal proliferation of plasma cell that causes destructive skeletal lesions and secondary systemic effects, and is a systemic disease diagnosed in the presence of light chain (Bence Jones) proteinuria, lytic skeletal lesions, and characteristic pathology. It accounts for about 10% of the hematological malignancies, with an incidence of 5.5 cases per 100,000 inhabitants [1]. We report the case of a 50-year-old man who presented right exophthalmos with Magnetic Resonance (MRI) evidence of a retro-orbital mass and with a clinical and pathological history of MM

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