Volume 25, Issue 118, December 2021

Hyaline fibromatosis: Two case reports and literature review

Abdulatif Abuhaimed¹, Meshal Almunif¹, Mashaal Alswaidan², Sarah Aldosari^3♦, Abdulmalik Alsahhaf³

¹Department of Oral and Maxillofacial Surgery, King Abdulaziz Medical City, National Guard, Riyadh, Saudi Arabia
²Saudi Board of Oral and Maxillofacial Surgery, Riyadh, Saudi Arabia
³College of Dentistry, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia

^♦Corresponding author
College of Dentistry, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia

ABSTRACT

Hyaline fibromatosis (HF) is a rare genetic disease, with two types that have an early onset. The disease is distinguished by hyaline deposition at different areas in the body, osteolytic bony lesions, and gingival hypertrophy. There are two variants of the disease, juvenile and infantile HF. In this report, we present two cases of HF that were seen in National Guard Hospital within Riyadh – Kingdom of Saudi Arabia.

Keywords: Juvenile; Hyaline; Infantile; Fibromatosis; Autosomal

Medical Science, 2021, 25(118), 3530-3534

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