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Published on: November 5, 2019
Idiopathic facial swelling secondary to sickle cell anaemia
Swapnil Moghe1, Ajay Pillai, Kanishka Navin Guru
1Department of Oral & Maxillofacial Surgery, People's Dental Academy, Bhopal, Madhya Pradesh, India.
Abstract:
Sickle cell disease is a common inherited autosomal disease that is characterised by abnormally shaped (sickle-shaped) red blood cells (RBCs). It can involve virtually any organ system. The clinical manifestations of sickle cell disease vary and are classified as vaso-occlusion, chronic anaemia and infection. The imaging appearances of central nervous system and musculoskeletal involvement by sickle cell disease have been well documented; however, involvement of the head and neck region is often unreported, although it is not uncommon. In the head and neck, sickle cell disease can involve the inner ears, orbits, paranasal sinuses, bones, lymph nodes and vessels. This paper describes a case of idiopathic facial swelling associated with sickle cell disease in a young patient.
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