Hereditary gingival fibromatosis (HGF) is a rare disorder characterized by progressive and varying degrees of gingival overgrowth. Oral manifestations may vary from minimal involvement of only tuberosity area and the buccal gingiva around the lower molars to a generalized gingival enlargement. It can occur as an isolated disorder but can be one feature of a syndrome. Although the clinical and h...

Fibromatosis is a non-metastatic, however locally invasive tumor that may infiltrate muscle, fat, and bone. It may be fatal depending on its location. Tumors in the head and neck are particularly dangerous. These fibroblast tumors have poorly defined margins and are not encapsulated. Anaplasia and invasion of nerves and vessels are not present; mitosis is rare and there may be collagen between ...

Gingival fibromatosis (GF) is a fibrous overgrowth of gingiva that maybe idiopathic or may have an inheritance pattern wherein it is known as hereditary gingival fibromatosis (HGF). This case report describes a 16-year old female patient who presented generalized extensive gingival overgrowth, involving the maxillary and mandibular arches. Diagnosis of GF was substantiated by the patient’s clin...

Hereditary gingival fibromatosis is a rare genetic disorder resulting in gingival overgrowth that can be found in both dental arches. As a result of the gingival overgrowth and associated dental displacement, affected patients occasionally present with increased occlusal vertical dimension and/or inadequate lip closure. Depending on the disorder's severity, these patients can be challenging to ...

Proliferation of fibrous tissues to form a localised mass with infiltrating margins may occur anywhere in the body; involvement of the orbit is rare. Children and young adults are most commonly affected. The term 'juvenile fibromatosis' is one of several synonyms. Of the two main forms of this entity, the solitary form is the more common and the prognosis is good. The multicentric form has a po...

Introducción: La Fibromatosis Colli es un tumor fibroso congénito benigno que se desarrolla en el músculo esternocleidomastoideo. Se manifiesta clínicamente por hinchazón del cuello y restricción de movimiento (tortícolis). 
 Objetivo: Describir los aspectos diagnósticos terapéuticos fundamentales la o Tortícolis Muscular Congénita.
 Caso Clínico: presenta caso neonato sexo femenino 2...

Peritonitis is a very rare complication of mesenteric fibromatosis. A case is reported which occurred 6 days post-partum. It is suggested that such lesions are hormone-sensitive.