Abstract

Giant cell arteritis (GCA) is a systemic vasculitis of medium and large arteries that mainly affects the external carotid artery. It is a diagnosis of the elderly that typically presents as low-grade fever, temporal tenderness, claudication of the jaw, and in some patients vision loss. In cases where GCA presents with atypical manifestations, the diagnosis may be more difficult, causing a delay in both diagnosis and treatment and ultimately leading to irreversible complications. In this paper, we present an atypical presentation of GCA with symptoms of neck swelling and lingual pain in an elderly female. These symptoms progressed to bilateral necrosis and eventual dislodgement of the tongue. Lingual necrosis is a severe potential complication in GCA. In patients presenting with lingual swelling, pain, and discoloration, GCA should be suspected and prompt therapy should be initiated to avoid irreversible complications.

Highlights

  • Giant cell arteritis is a chronic vasculitis of large and medium sized vessels that commonly affects those above the age of 50 years

  • This paper presents a case of lingual pain and bilateral tongue necrosis secondary to Giant cell arteritis (GCA) along with a literature review of this rare complication

  • This paper presents a case of bilateral tongue necrosis and eventual self-amputation of the tongue as a rare complication of GCA

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Summary

Introduction

Giant cell arteritis is a chronic vasculitis of large and medium sized vessels that commonly affects those above the age of 50 years. It has an estimated incidence of 20 cases per 100,000 individuals and a prevalence of 1 in 500 individuals [1]. The diagnosis of GCA is clinicopathological for which the American College of Rheumatology (ACR) has established classification criteria. Lingual necrosis is a known complication of GCA that commonly affects one side of the tongue [5,6,7,8]. This paper presents a case of lingual pain and bilateral tongue necrosis secondary to GCA along with a literature review of this rare complication

Case Report
Literature Review
Discussion
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