Abstract

Multiple myeloma is a malignant plasma-cell disorder that primarily involves the bone marrow, but extramedullary involvement is becoming increasingly common (Bladé et al., 2012) both at initial presentation and follow-up. Most common initial presentations for multiple myeloma include generalized fatigue, renal insufficiency, bone pain, and recurrent bacterial infections. We present a case of a healthy 55-year-old man that presented to the emergency department with a three-week history of anorexia and jaundice without any past medical history. Patient's initial labs were significant for hyperbilirubinemia and elevated liver function enzymes (AST, ALT, ALP, and GGT). Additional laboratory workup was significant for mild hypercalcemia and increased protein gap. MRI and ERCP suggested primary sclerosing cholangitis but were not diagnostic. Liver biopsy illustrated plasma-cell infiltration and bone marrow biopsy diagnosed multiple myeloma with extramedullary disease. Patient was started on dexamethasone, bortezomib, and cyclophosphamide, but, despite this aggressive regimen, the patient continued to decline. We take this opportunity to present this atypical presentation of a common hematological malignancy and review the associated literature.

Highlights

  • Multiple myeloma accounts for one percent of human cancers, almost two percent of cancer deaths, and 12–15% of all hematological cancers [1]

  • Myeloma is thought to arise from monoclonal gammopathy of undetermined clinical significance that progresses to smoldering myeloma and, to symptomatic myeloma [1,2,3]

  • We report a case of a 55-year-old man who presented with jaundice and abdominal pain as the initial clinical manifestations of multiple myeloma

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Summary

Introduction

Multiple myeloma accounts for one percent of human cancers, almost two percent of cancer deaths, and 12–15% of all hematological cancers [1]. It is a neoplastic plasmacell disorder that involves clonal proliferation of malignant plasma cells in bone marrow, monoclonal protein in the blood or urine, and involved organs. The diagnosis requires presence of 30% monoclonal bone marrow plasma cells and most common initial presentations include anemia (73%), bony lesions (80%), and renal impairment (20–40%) [1]. Multiple myeloma is a malignancy that predominantly affects bone marrow and bone, involvement of extraosseous tissues like spleen and liver is a relatively frequent postmortem finding [4,5,6]. The reported incidence of liver involvement in myeloma has been reported to be in the range of 26% to 46% in autopsy studies [7]. We report a case of a 55-year-old man who presented with jaundice and abdominal pain as the initial clinical manifestations of multiple myeloma

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