PDF | The majority of oral diseases present as growths and masses of varied cellular origin. Such masses may include simple hyperplasia. The presence of a neurovascular hamartoma within the oral cavity is truly a rare entity. Scarcely reported in the literature, these hamartomas. Cowden’s Syndrome, Bannayan-Riley-Ruvalcaba Syndrome, PTEN Hamartoma Tumour Syndrome.

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J Bras Patol Med Lab. To conclude, hamartomas should promptly be included in the differential diagnosis of the tumours of oral cavity, essentially the paediatric tumours, to avoid aggressive treatment and morbidity. Essentially, understanding the dynamics of each of these disease processes forms an integral part of the appropriate treatment planning.

National Center for Biotechnology InformationU. Current management hamratomas hemangiomas and vascular malformations. WHO Publications Center; Department of Oral Pathology and Microbiology, M. Nevi or mole represents collection of nevus cells which are derivatives of melanocytes or their precursor neural crest cells.

You can decide to make it visible only to you or to a restricted audience. Chau et al suggested ameloblastic fibroma as a distinct entity from ameloblastic fibroodontome with neoplastic potential [23]. Clinicopathologic presentation of 3 cases.


Hamartomas of the oral cavity Patil S, Rao RS, Majumdar B – J Int Soc Prevent Communit Dent

These years can be or by uncertainty, multiple hospital attendances, investigations, misdiagnoses, and inappropriate treatments; with huge emotional cost and wasted time, effort and resources. Fibrolipomatous hamartoma in a patient with tuberous sclerosis: Developmental disordershamartomaoral cavitysyndrometumour.

Oral-facial-digital syndrome type 1. Irregularly formed cemental matrix with entrapped cells.

Hamartomas of the oral cavity

Case Rep Dent Expression of extracellular matrix proteins in ameloblastoma hamartoams adenomatoid odontogenic tumors. Ameloblastic layer can be seen attached to the formed enamel like matrix. Expression of extracellular matrix proteins in ameloblastoma and adenomatoid odontogenic tumors. Caution with radiotherapy is recommended until this observation can be studied further in larger cohorts of Cowden syn- drome patients.

How do I publish content on my topic? Ethunandan M, Mellor TK.

How to grow my audience and develop my traffic? The odontogenic islands resemble ameloblastic islands which show peripheral arrangement of columnar to tall cuboidal cells. The mechanism of formation of these tubular structures is not entirely clear but is likely the result of the secretory activity of the tumor cells, which appear to be preameloblasts in nature [29].

J Appl Oral Kf ; The predominant histology is papillary renal otal carcinoma [Mester et al ]. Focal areas showing calcifications. Odontogenic Tumors and Allied Lesions; pp.


Int Endod J ; A Concise Textbook of Surgery. Pathol Res Pract ; It is a rare lesion of the minor salivary glands. The tubular or duct-like structures may be predominant, scanty, or even absent in a given section. Numerous cords of odontogenic epithelium and attempts of hard tissue formation. Although multiple organ systems are frequently involved, the target organs more frequently affected are the skin nevoid basal cel.

Hamartomas of the oral cavity

Microscopically, it comprises of odontogenic epithelium and calcifications. The tumour mostly occurs in the children and young adults, though seen in other age groups too.

Rhabdomyomatous mesenchymal hamartoma It is an exceptionally rare congenital lesion of the oral cavity. Hamartomas are commonly observed in lung, pancreas, spleen, liver and kidney. The strand often exhibits double or triple layer of cuboidal cells which has a close resemblance to dental lamina.

By redirecting your social media traffic to your website, Scoop. Multiple leiomyomatous hamartoma in the oral cavity.

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