{Reference Type}: Case Reports
{Title}: Congenital infantile digital fibromatosis: a case report and review of the literature.
{Author}: Adegoke OO;Ajao AE;Ano-Edward GH;
{Journal}: Afr Health Sci
{Volume}: 20
{Issue}: 4
{Year}: Dec 2020
{Factor}: 1.108
{DOI}: 10.4314/ahs.v20i4.42
{Abstract}: Infantile digital fibromatosis (IDF), also called inclusion body fibromatosis is an uncommon benign tumour occurring in the digits of young children. In about a third of cases, it is congenital and the diagnosis is based on the presence of peculiar intracytoplasmic inclusions on histology. Recurrence rate post-surgery is high. However, spontaneous regression has been reported. We present a case of a 5-month-old infant who had excision of a right second toe mass, which has been present from birth. Histological examination revealed this to be infantile digital fibromatosis. To the best of our knowledge, no report of this has been made in Nigeria. It is important that this diagnosis be entertained in young children with masses on the digits as this will influence the management instituted.