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Table 31-4 Clinical syndromes caused by tumors at the base of the skull (see also Tables 47-1 and 47-2)

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580 Rochon-Duvigneau; syndrome of the pterygopalatine fossa (Behr) and the base of the orbit (DeJean) commencing with a lesion of the maxillary and pterygoid rami and evolving into the superior orbital ssure syndrome Jacod-Rollet (often combined with the syndrome of the superior orbital ssure); infraclinoid syndrome of Dandy Foix-Jefferson; syndrome of the sphenopetrosal ssure (Bonnet and Bonnet) corresponding in part to the cavernous sinus syndrome of Raeder Gradenigo-Lannois Lesions of the third, fourth, sixth, and rst divisions of the fth nerves with ophthalmoplegia, pain, and sensory disturbances in the area of V1; often exophthalmos, some vegetative disturbances Visual disturbances, central scotoma, papilledema, optic nerve atrophy; occasional exophthalmos, chemosis Ophthalmoplegia due to lesions of the third, fourth, sixth, and often fth nerves; exophthalmos; vegetative disturbances Jefferson distinguished three syndromes: (1) the anterior-superior, corresponding to the superior orbital ssure syndrome; (2) the middle, causing ophthalmoplegia and lesions of V1 and V2; (3) the caudal, in addition affecting the whole trigeminal nerve Lesions of the fth and sixth nerves with neuralgia, sensory, and motor disturbances, diplopia

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XHTML rather than in ABAP format This allows the BEx Web Analyzer to create the variants both global and local

Tumors that invade the anterior part of the base of the skull from the frontal sinus, nasal cavity, or the ethmoid bone, osteomas Meningiomas of the olfactory groove Tumors: meningiomas, osteomas, dermoid cysts, giant-cell tumors, tumors of the orbit, nasopharyngeal tumors; more rarely optic nerve gliomas; eosinophilic granulomas, angiomas, local or neighboring infections, trauma Optic nerve glioma, infraclinoid aneurysm of the internal carotid artery, trauma, orbital tumors, Paget disease Tumors of the sellar and parasellar area, infraclinoid aneurysms of the internal carotid artery, nasopharyngeal tumors, stulas of the sinus cavernosus and the carotid artery (traumatic), tumors of the middle cranial fossa, eg, chondromas, meningiomas, and neurinomas

In ammatory processes (otitis), tumors such as cholesteatomas, chondromas, meningiomas, neurinomas of the gasserian ganglion and trigeminal root, primary and secondary sarcomas at the base of the skull

Tumors of the sphenoid and petrosal bones and middle cranial fossa, nasopharyngeal tumors, metastases

Anterior occipital condyles Collet-Sicard (Vernet-Sargnon)

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Let s look at a very basic variant that is created From the Web side, you can now create a variant so that your business users can be responsible for this process, and you will probably only allow them to create local variants variants that they set up for themselves and that can t be used by anybody else If you decide to allow global variants, once these variants are available, they are available for all business users

Retroparotid space (retropharyngeal syndrome) Villaret Garcin (Guillain-Alajouanine-Garcin); also described by Hartmann in 1904

Tumors of the glomus jugulare; neurinomas of eighth, ninth, tenth, and eleventh nerves; chondromas, cholesteatomas, meningiomas, nasopharyngeal and ear tumors; infections, angiomas, rarely trauma Tumors of the base of the skull, ear, parotid; leukemic in ltrates; aneurysms, angiomas, and in ammations Tumors of the retroparotid space (carcinomas, sarcomas), trauma, in ammations Nasopharyngeal tumors, primary tumors at the base of the skull, leukemic in ltrates of basal meninges, trauma, metastases Acoustic neuromas (raised protein in CSF), meningiomas, cholesteatomas, metastases, cerebellar tumors, neurinomas of the caudal group of nerves and the trigeminal nerve, vascular processes such as angiomas, basilar aneurysms

Ophthalmoplegia due to loss of function of the third, fourth, and sixth nerves; amaurosis; trigeminal neuralgia possibly with sensory signs Lesions of ninth, tenth, and eleventh nerves with disturbance of deglutition; curtain phenomenon; sensory disturbances of the tongue, soft palate, pharynx, and larynx; hoarseness; weakness of the sternocleidomastoid and trapezius Loss of twelfth nerve function (loss of normal tongue mobility) in addition to the symptoms of the jugular foramen Lesions of the lower group of nerves (ColletSicard) and Bernard-Horner syndrome with ptosis and miosis Loss of function of all twelve cranial nerves of one side; in many cases, isolated cranial nerves spared; rarely signs of raised intracranial pressure or pyramidal tract symptoms Loss of function of eighth nerve (hearing loss, vertigo, nystagmus); cerebellar disturbances; lesions of the fth, seventh, and possibly ninth and tenth cranial nerves Signs of raised intracranial pressure, brainstem symptoms

Start by creating a variant from the Web The following illustration shows the variable screen used to create the variant

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