Hyper-IgE syndrome caused by DOCK8 mutation with a tumour-like lesion of the lip: a case report

paythelady.61 shared this article with you from Inoreader Hyper-IgE syndrome caused by DOCK8 mutation with a tumour-like lesion of the lip: a case report Via International Journal of Oral and Maxillofacial Surgery Autosomal recessive hyper-IgE syndrome caused by DOCK8 gene mutation is an immunodeficiency. However, the presentation of a tumour-like lesion of the lip in autosomal recessive hyper-IgE syndrome has not yet been reported. This article reports the case of a 20-year-old man with autosomal recessive hyper-IgE syndrome who presented with a tumour-like lesion of the lip, and hyperplasia and erosion of the gingiva. The clinical manifestations included coarse face and neck skin, a diffuse tumour-like lesion on the upper lip showing a reddish erosive nodular surface with yellowish-white exudation, erosive buccal mucosa, and severe periodontitis. View on the web Inoreader. Take back control of your news feed. Follow us on Twitter and Facebook.