No abstract available.http://www.springerlink.com/content/100510

Adroos, Narosha

Kruger, Henk

Lockhat, Zarina I.

Muller, Craig

Slavik, Tomas

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Toothy Craniopharyngioma: A literature review and case report ofCraniopharyngioma with extensive odontogenic differentiation and toothformationDr Craig Muller.MBChB(University of Witwatersrand)Department of RadiologySteve Biko Academic HospitalUniversity of PretoriaDr Narosha AdroosMBChB (University of Pretoria), MMed (Rad D) (University of Pretoria)Department of RadiologySteve Biko Academic HospitalUniversity of PretoriaProf Zarina LockhatMBChB (University of Natal), FC (Rad D) (SA)Department of RadiologySteve Biko Academic HospitalUniversity of PretoriaDr Tomas SlavikMBChB (University of Pretoria), MMed (Anatomical Pathology) (University of Pretoria), FC Path (SA)Dr Henk KrugerMBChB(University of Orange Free State), MMed (Neurosurgery) (University of Pretoria)Corresponding author:Dr Craig Mullerdrcraigmuller@gmail.comIntroduction:A young child presenting with a craniopharyngioma (pituitary adamantinoma) demonstrated therare phenomenon of pronounced odontogenic elements / tooth formation on imaging.  The origin ofthe craniopharyngioma from primitive stomatodeum theoretically facilitates odontogenesis (1).Theories of the genesis of this tumour include remnants of the craniopharyngeal duct, squamousmetaplasia of anterior pituitary cells and misplaced tissue of the embryonic enamel organ (2).  Aliterature review documents six cases of craniopharyngioma with tooth formation although noneappear to be as extensive as the case presented. Craniopharyngioma should be added to teratoma inthe differential diagnosis of suprasellar odontogenic elements demonstrated by imaging studies.Case report:A 2 year 9 month old girl presented with headache and irritability after sustaining head traumaduring a fall. In addition the parents noticed the child’s poor vision, delayed milestones and morerecent progressive left pupillary dilation and left-sided ptosis.  An initial CT scan of the braindemonstrated a large well circumscribed tumour centred on the suprasellar region but also involvingand expanding the pituitary fossa. The striking feature of the mass was the presence of innumerablediscreet high density elements resembling teeth (Fig 1 a, b and c and Fig 2 a, b). It was difficult tofully assess the intervening soft tissue component due to artefact caused by the densely calcifiedelements. There was significant mass effect on the structures of the middle fossa with obstructivehydrocephalus.  The age of the child and the imaging characteristics led to a preliminary diagnosis ofteratoma.The patient was referred for an emergency shunt procedure.  A post-shunt plain film examination ofthe skull was performed for shunt evaluation. This demonstrated the surgical shunt, splaying of thecranial sutures and a copper beaten / lacunar calvarium reflecting chronic raised intracranialpressure. The odontogenic elements of the tumour were also clearly demonstrated as well asexpansion of the pituitary fossa (Fig 3).The patient also had an MRI of the brain for pre operative planning (Fig 4 a, b and c).   The mass wasclearly delineated with internal focal low signal intensity foci on T1W, T2W and GRE sequences inkeeping with the calcified odontogenic elements. The intervening soft tissue component was iso tolow signal on T1W and high signal on T2W and FLAIR. Post administration of gadolinium the softtissue component demonstrated heterogeneous enhancement. The adjacent brain parenchymashowed minimal oedema. The left lateral ventricle was decompressed by the previously insertedshunt; however the right lateral ventricular system remained obstructed at the level of theinterventricular foramen. The pituitary gland and hypothalamic structures could not be clearlydiscerned from the tumour mass.At surgery the tumour was approached from the right fronto-temporal region with opening of theSylvian fissure. The tumour mass was exposed and the optic nerves/chiasm and circle of Willis wereidentified.   In order to remove the tumour, each tooth had to be individually resected. There wereno intra operative complications and the patient was extubated post operatively with no newneurological signs.During the first two post operative days the child seemed to be making a good recovery. However onthe third day the patient developed diabetes insipidus. Cerebral oedema and neurogenic pulmonaryoedema followed and the patient unfortunately died due to hypothalamic crisis.Histological examination of the tumour revealed an adamantinomatous craniopharyngioma withpronounced odontogenic elements.Microscopic examination confirmed the characteristic histology of craniopharyngioma(adamantinomatous-type), with a small amount of adjacent premorbid adenohypophysis (Fig 5).Additionally, odontogenic rests and pronounced odontogenic differentiation was present in thesurrounding fibrous stroma which revealed multiple well-formed teeth (Fig 6 and 7). The latterdemonstrated an organoid appearance with central dental papilla, adjacent odontoblastic layer,dentine, enamel, external ameloblasts and peripheral enamel organ. No definite endo-/meso-/ectodermal teratomatous elements were identified.Discussion:Craniopharyngioma is considered the commonest intracranial tumour of childhood and adolescenceaccounting for 8.3% of intracranial tumours and 14.5% of all supratentorial tumours.  These tumoursgrow as a pseudoencapsulated mass, usually in a suprasellar location and less commonly areintrasellar. Suprasellar tumours are usually both solid and cystic.  Although they often destroy thepituitary, they may also grow toward the third ventricle, optic chiasm and tract, pons and thalamus.Through continued growth and pressure, the sella turcica is destroyed, as is the pituitary (2).Craniopharyngiomas are classically divided into two subtypes: adamantinomatous and papillary. Theadamantinomatous subtype is most commonly found in the paediatric age group and usuallypresents as a complex mixed cystic and solid mass which characteristically contains flecks ofcalcification (3).  On MR imaging the cystic component is usually hyperintense on T1W due to thehigh protein content of the cysts while the solid component is usually of heterogeneous signal onT1W and T2W images. The solid component enhances heterogeneously. Gradient echo sequencesare useful for the presence of calcification confirmed by demonstrating a ‘blooming artefact’.  Thepapillary subtype is more common in the adult population (>50years) and is more commonly solidand less likely to contain calcification than the adamantinomatous subtype (3).  Our case did notdemonstrate typical features of craniopharyngioma.Many theories have been postulated regarding the origin of these tumours and include:1. Epithelial rests and craniopharyngioma arising from a portion of an incompletelyobliterated craniopharyngeal duct (4).2. A metaplastic process where squamous cells might arise from other cell types.3. The tumour could arise by an inrolling of dental elements into the tuberal process ofthe developing pituitary (5).  Whether the tumour arises from embryonic residues ormetaplasia, the similarity to the adamantinoma of the jaw is valid only if theembryonic ductal epithelium remains competent to differentiate in this direction (6).The differential diagnosis includes epidermoid, dermoid and teratomas (2).Conclusion:The diagnosis of craniopharyngioma is usually made when a tumour exhibits the classic imagingfeatures. The presence of tooth like structures within a tumour primarily raises suspicion forteratoma. The intimate embryological origin of tumours arising from Rathkes Pouch should be keptin mind when diagnosing tumours in the sellar / suprasellar region.References1. Alvarez-Garijo, Froufe A, Taboada D, Vila M.  Successful surgical tretmant of anondontogenic ossified craniopharyngioma.  Case report.  J. Neurosurgery.  1981; 55: 832-8352. Seemayer TA, Blundeall JS, Wiglesworth FW.  Pituitary craniopharyngioma with toothformation.  Cancer. 1972; 29; 423-4303. Osborn AG, Et al.   Diagnostic Imaging Brain.  Amirsys, II:2:32-354. Critchley M, Ironside RN.  The pituitary adamantinomata.  Brain. 1926;  49:  4375. Love JG, Marshall TM.  Craniopharyngioma.  Surg. Gynecol Obstet. 1960; 90; 5916. Evans RW.  Histological Appearances of Tumors.  Edinburgh and London, E and S. LivingstoneLtd.,  1966ImagesFigure 1a, b, and c:  Axial Pre-contrast CT scan reveals a large dense lesion.  Bone algorithmreveals the densely calcified elements            a                                          b                                        cFigure 2 a and b:  Coronal and sagittal reconstructions demonstrate the supra-sellar location ofthe lesion               a                                 bFigure 3:  Lateral skull radiograph reveals the position of the VP shunt, the splaying of thesutures and the “copper beaten skull” appearanceFigure 4 a, b and c:  Axial T2 and T1 post gadolinium coronal and sagittal images demonstratesthe ‘blooming’ artefact of the dense calcifications as well as the supra-sella location of the mass               a                                             b                                       cFigure 5:  Conventional adamantinomatous-type craniopharyngioma component (arrows) in relationto premorbid adenohypophyseal tissue (asterisks) (H & E, original magnification x 100)Figure 6:  Primitive odontogenic mesenchyme and epithelium with rudimentary tooth formation (H& E, original magnification x 100)Figure 7:  One of multiple tooth structures demonstrating readily identifiable dental pulp,dentine, enamel and surrounding odontogenic epithelium (H & E, original magnification x 40).

Toothy craniopharyngioma : a literature review and case report of craniopharyngioma with extensive odontogenic differentiation and tooth formation

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Toothy craniopharyngioma : a literature review and case report of craniopharyngioma with extensive odontogenic differentiation and tooth formation

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