EPULIS FIBROSA PDF

The fibrous epulis, a common tumor-like lesion of the gingiva, appears in the interdental papilla as a result of local irritation. Lesions are. For the purpose of clinical diagnosis, enlargements mentioned in this review are grossly are divided into isolated lesions (epulis) and regional or generalized. Fibroid mass in free gingiva, due to chronic gingival inflammation, pyogenic granuloma or other causes; May calcify or ossify. Terminology.

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Orofacial soft tissues — Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig’s angina Macrostomia Melkersson—Rosenthal syndrome Microstomia Noma Oral Crohn’s disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans. There are no specific tests for sarcoidosis. Usually at the initial presentation there is no pain.

Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease. It is also called Neumann’s tumor. Analysis of the surgical specimen. Oral cavity Congenital anomalies Epulis Author: Signs and symptoms related to gingival enlargement are seen within mo of initiation of drug intake.

When infected secondarily, there is increase in the size of existing enlargement and adds characteristic features of inflammatory enlargement. Granulomatous gingivitis in Anderson-Fabry disease. Ultrastructural investigation of Zimmermann-Laband syndrome. Published online Sep Periodontal management of gingival enlargement associated with Sturge-Weber syndrome.

Published by Baishideng Publishing Group Inc. Severe mid face retraction, severe mental retardation and congenital heart defect, patient usually die under 10 yr of age.

When patients are in combination therapy, in which two or more drugs are known to cause gingival enlargement, then, which should be attributed to the diagnosis fibrisa DIGO, is a puzzle. We believe that the controlled excision of adjacent periodontal membrane, periostium and alveolar bone, and the root planning performed to eliminate irritations were essential to avoid the recurrence.

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Nasopalatine duct Median mandibular Median palatal Traumatic bone Osteoma Osteomyelitis Osteonecrosis Bisphosphonate-associated Neuralgia-inducing cavitational osteonecrosis Osteoradionecrosis Osteoporotic bone marrow defect Paget’s disease of bone Periapical abscess Phoenix abscess Periapical periodontitis Stafne defect Torus mandibularis.

Unusual firm fibrotic gingival enlargements in a patient with fibroa gingival fibromatosis. Page views in Oral hobnail hemangioma–a case report.

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Enamel hypoplasia, multiple small red papules of lips, early onset periodontitis and repeated oral candidiasis, signs of cirrhosis.

Squamous cell papilloma Keratoacanthoma Malignant: Gingival abscess, near gingival margin or papilla; B: Periapical, mandibular and maxillary hard tissues — Bones of jaws.

Palate Bednar’s aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus. Idiopathic gingival enlargement is also referred to as congenital familial fibromatosis, gingivomatosis, idiopathic fibromatosis, elephantiasis and hereditary gingival hyperplasia.

Retrieved from ” https: Click here for information on linking to epuliis website or using our content wpulis images. Reactive lesions of the gingiva. Rutherfurd syndrome associated with Marfan syndrome. Hereditary gingival fibromatosis and sensorineural hearing loss in a year-old man with Jones syndrome. Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker’s melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga—Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus.

They occur particularly in anterior region in young patients fibroxa in posterior mouth during mixed dentition phase and in adults. It is normally associated with swelling of lips, bowel disorders, fever and ulcers.

Based on the existing knowledge and clinical experience, a differential diagnosis can be formulated. In these cases, it becomes difficult to eoulis duration of occurrence of enlargement with related drug history.

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When traumatized, the lesion contain inflammatory infiltrate and ulcerated area will be covered with fibrin and organisms from the oral flora.

Lesion at 3 weeks.

A clinicopathological study of cases. Periapical, mandibular and maxillary hard tissues — Bones of jaws Agnathia Alveolar osteitis Buccal exostosis Cherubism Idiopathic osteosclerosis Mandibular fracture Microgenia Finrosa Intraosseous cysts Odontogenic: Tissue bits lined by stratified squamous epithelium, tumor is beneath. The localized epulis like lesions can also be classified as being benign or malignant.

Massive fibrous epulis—a case report of a 10-year-old lesion

The presentation begins as slight ballooning of the papilla or marginal gingiva, depending upon the location of the irritant. Moreover, the great majority of localized overgrowths of the gingiva are considered to be reactive rather than neoplastic in nature.

The appearance of an epulis fissuratum microscopically is an overgrowth of cells from the fibrous connective tissue. Retrieved from ” https: Generalized gingival hyperplasia, during pregnancy and puberty, is influenced by hormonal changes that pretentious the response to local irritants. Cowden syndrome[ 31 ]. Diagnosis can be made by a positive family history of gingival enlargement. An expeditious diagnosis can be made by a simple full blood count.

Pathology Outlines – Epulis

Fibroza protruding from mouth. Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease. In a typical bimaxillary protrusion case, the enlargement will be limited to palatal aspect of maxillary anteriors and labial aspect of mandibular anteriors. The etiology of this entity is difficult to establish, but it is considered to be a hypersensitivity reaction with affluent plasma cells seen histologically.