A rare coexistence of Behcet’s disease and Graves’ thyrotoxicosis in a young man: a case report

Author:

Joshi Hareesh1ORCID,Shahriar Imran1,Sharma Poonam2,Sagi Satyanarayana V1,Oyibo Samson O1

Affiliation:

1. Department of Diabetes and Endocrinology, Peterborough City Hospital, Peterborough, UK

2. Department of Rheumatology, Peterborough City Hospital, Peterborough, UK

Abstract

Abstract Behcet’s disease is a recurrent systemic vasculitic disorder. It manifests most commonly in the form of skin lesions, oral and genital ulcers and uveitis. Graves’ thyrotoxicosis is an autoimmune disorder characterized by excessive production of thyroid hormones. We present a case of a 41-year-old male of Turkish descent who had symptoms of arthralgia, rash, palpitations and weight loss. Bloods tests showed raised inflammatory markers and biochemical evidence of severe autoimmune thyrotoxicosis. The patient was HLA-B51-negative, and pathergy test was inconclusive. A diagnosis of Behcet’s disease was made on constellation of clinical symptoms. The patient was treated with carbimazole and prednisolone followed by azathioprine. The coexistence of Behcet’s disease and Graves’ disease in the same patient is very rare. Further studies are required to determine if there is a pathological association between these two conditions.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Embryology,Anatomy

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