Pseudoepitheliomatous hyperplasia of oral epithelium
overdiagnosis of SCCA
Overlookedgranularcells
CONGENITAL EPULIS OF THE NEWBORN other name
Congenital Gingival Granular Cell Tumors
MX Anterior gingiva of newborns
CONGENITAL EPULIS OF THE NEWBORN
SCHWANNOMA Other name
Neurilemmoma
Favored location SCHWANNOMA
tongue
sometimes thought due to intralesional hemorrhage)
SCHWANNOMA
palisaded whorls and waves, surround acellular eosinophilic zone (verocay body) representing reduplicated BM and cytoplasmic cellular processes
Antoni A areas
spindle cells haphazardly distributed in a delicate fibrillar microcystic matrix, by immunochemistry tumor strongly expresses S-100 protein, (-) stains for actin and desmin
Antoni Btissue
(microscopic variant) has been described to designate degenerative changes in long-standing schwannoma
Ancient schwannoma
Neurofibromatosis syndrome
von Recklinghausen’s disease of skin
NEUROFIBROMA 2 subsets:
NF1 and NF2 gene
Most common site
tongue, buccal mucosa and vestibule
Oral lesions are associated with
NF1
enlarged fungiform papillae and bone abnormalities; oral manifestations seen in 70% of NF cases
Oral stigmata
>= 6 café-au-lait macules at any location >1.5cm in diameter = suggestive of neurofibromatosis
axillary freckling
Crowe’s sign
iris freckling
Lisch spots
Most common site in Md NEUROFIBROMA
mandibular nerve
MD involvement: accompanying radiographic sign may be the formation of a flaring of inferior alveolar foramen, the so-called
blunderbuss foramen
Comprise a group of conditions characterized by neoplasms arising in several endocrine organs
MUCOSALNEUROMA OF MULTIPLE ENDORCINE NEOPLASIA SYNDROMETYPE III
MEN type III
MEN 2b
has oral manifestations (autosomal dominant trait)
MEN type III aka MEN 2b
MEN III is caused
RET oncogene
RET Gene is responsible for
MEN II (MEN 2a)
Oral lesions men
tongue, lips and buccal mucosa
benign neoplasm that produces catecholamines that may cause significant