Papilliferous keratoameloblastoma: an extremely rare case report
- PMID: 23862079
- PMCID: PMC3686074
- DOI: 10.1155/2013/706128
Papilliferous keratoameloblastoma: an extremely rare case report
Abstract
Odontogenic tumors develop in the jaw bones from the odontogenic tissue-oral epithelium in tooth germ, enamel organ, dental papilla, reduced enamel epithelium, remnants of Hertwig's root sheath or dental lamina, and so forth. Hence, a bewildering variety of tumors are encountered in the maxilla and mandible. Ameloblastoma is the second most common odontogenic neoplasm after odontomes, and it has numerous clinical and histologic variants. We report a very rare histologic variant: the papilliferous keratoameloblastoma which is the fifth reported case in the English literature.
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References
-
- Shafer WG, Hine MK, Levy BM. A Textbook of Oral Pathology. 4th edition. Philadelphia, Pa, USA: WB Saunders; 1983.
-
- Takeda Y, Satoh M, Nakamura S, Ohya T. Keratoameloblastoma with unique histological architecture: an undescribed variation of ameloblastoma. Virchows Archiv. 2001;439(4):593–596. - PubMed
-
- Altini M, Slabbert HD, Johnston T. Papilliferous keratoameloblastoma. Journal of Oral Pathology and Medicine. 1991;20(1):46–48. - PubMed
-
- Whitt JC, Dunlap CL, Sheets JL, Thompson ML. Keratoameloblastoma: a tumor sui generis or a chimera? Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology. 2007;104(3):368–376. - PubMed
-
- Pindborg JJ. Pathology of the Dental Hard Tissues. Philadelphia, Pa, USA: WB Saunders; 1970.
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