Hereditary gingival fibromatosis (HGF), also known as idiopathic gingival hyperplasia, is a rare condition of gingival overgrowth. HGF is characterized as a . Hereditary, drug-induced, and idiopathic gingival overgrowth have been reported . Hereditary gingival fibromatosis can occur as an isolated. Mutation in SOS1, son-of-sevenless gene, is thought to be responsible for hereditary gingival fibromatosis. This report shows a case of.
|Published (Last):||22 October 2006|
|PDF File Size:||12.23 Mb|
|ePub File Size:||17.12 Mb|
|Price:||Free* [*Free Regsitration Required]|
Panoramic radiograph showing normal development of permanent teeth and missing of maxillary right first and left second premolars. Researchers approached this fibromatossi with periodontics – a partial gingivectomy and flap surgery.
There was no associated pain and bleeding noted. Hereditary gingival fibromatosis HGF is a benign, non-hemorrhagic, fibrous gingival overgrowth that can cover all or part of the teeth. Although the genetic mechanism is not fully understood, majority of research workers have attributed this condition related with hereditary factors.
New website online since 11 th Aug, Hereditary gingival fibromatosis associated with generalized aggressive periodontitis: Rubor Calor Tumor Dolor Functio laesa.
Hereditary gingival fibromatosis – Wikipedia
Only comments written in English can be processed. Report of an affected family with associated splenomegaly and skeletal and soft tissue abnormalities.
There are very few ways to test a patient for HGF. Radiography showed appropriate root development, with two thirds of the root formed Fig. The patient’s medical history did not reveal any drug induced gingival enlargement or hormonal changes and exhibited no signs of hypertrichosis or mental retardation that could be associated with gingival hyperplasia.
Case Reports in Dentistry
Hereditary gingival fibromatosis
The mandible was relatively thinner in angle region bilaterally. All the forms of HGF is not characterized histologically, especially some syndromic forms. It was suggested to the parents that surgery should be performed with nitrous oxide sedation and local anesthesia, opting for external bevel gingivectomy.
There was no associated lymphadenopathy noted. Familial gingival fibromatosis withunusual histologic findings. Routine blood investigations were gijgival and values were found within normal range although haemoglobin values was slightly below normal range 8. The symmetric type is most common type of gingival enlargement, however there may be combination of both types.
On the basis of clinical, radiological, and histopathological examination; a final diagnosis of HGF has been achieved. Published online February Additional information Further information on this disease Classification s 2 Gene s 3 Clinical signs and symptoms Publications in PubMed Other website s 0.
Hereditary gingival fibromatosis: Characteristics and treatment approach
HGF may be associated with other clinical manifestations such as hypertrichosis,[ 15 ] growth retardation,[ 16 ] hypopigmentation, mental deficiency,[ 17 ] epilepsy,[ 18 ] splenomegaly,[ 11 ] optic and auditory defects, cartilage and nail defects gereditary dentigerous cysts.
The symmetric form, which is the most common type of disorder, results in uniform enlargement of the gingiva that is firm, dense, resilient, insensitive fibrous tissue that covers the alveolar ridges and extends over the teeth resulting in extensive pseudo pockets. In the first case, internal bevel gingivectomy made it possible to view the bone crest and its relationship with the cemento-enamel line.
Fibromatoss Scaling and root planing Full mouth disinfection Full mouth ultrasonic debridement.
Epidemiology, pathogenesis and complications. The overlying epithelium was hyper-plastic with enlarged rete ridges.
Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease. Gingival overgrowth in children: Hart, Yingze Zhang, Michael C.