Brain Tumor and Clinical Findings

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Brain Tumor and Clinical

Findings
Sellar Tumour
INTRODUCTION
Sellar masses typically
present in one or more ways:
With neurologic symptoms,
such as visual impairment or
headache
With hormonal abnormalities
Etiology
Congenital
Ratche cleft cyst
Neoplasma
Craniopharingioma
Pituitary Adenoma
Vascular
aneurysms
Infection
Pituitary abscess
Pineal Regio Tumour
Parinaud's Syndrome
1.Paralysis of upgaze: Downward gaze is usually preserved.
2.Pseudo-Argyll Robertson Pupils: Accommodative paresis ensues, and pupils become mid-dilated and
show light-near dissociation.
3.Convergence-Retraction nystagmus: Attempts at upward gaze often produce this phenomenon. On fast
up-gaze, the eyes pull in and the globes retract.
4.Conjugate down gaze in the primary position: "setting-sun sign".
Medulloblastoma
most common type of pediatric malignant primary brain tumor
(cancer)
originating in the part of the brain that is towards the back and the
bottom, on the floor of the skull, in the cerebellum or posterior fossa.
By far, the cerebellum is the most common location for
medulloblastomas (94.4% of cases in the SEER study), and most
(>75%) of these arise in the midline cerebellar vermis (1,2). More
lateral locations within the cerebellar hemisphere are typical when
these tumors manifest in older children, adolescents, and adults
Clinical findings:

ICP due to secondary hydrocephalus


Truncal ataxia
One-third of patients have positive Babinski and Hoffmann signs
Abducens nerve palsy, resulting from compression of the relatively exposed
nucleus of the sixth cranial nerve along the anterior margin of the fourth
ventricle, is also a common manifestation of the extraventricular tumor
extension
Cerbello pontine Tumour
the most common neoplasms in the posterior fossa (5-10% )of
intracranial tumors.
Most are benign, 85% being vestibular schwannomas (acoustic
neuromas), lipomas, vascular malformations, and hemangiomas.
The most frequent nonacoustic CPA tumors are meningiomas,
epidermoids (primary cholesteatomas), and facial or lower cranial
nerve schwannomas.
Primary malignancies or metastatic lesions account for less than 2% of
neoplasms in the CPA.
Cerebello Pontine
Cerbello pontine Tumour
Meningioma
Trigeminal or facial nerve symptoms are likely to occur earlier than hearing
loss.
Patients with larger tumors can present with obstructive hydrocephalus
and/or symptoms of brainstem compression.
Epidermoid
These can become quite large without symptoms.
Facial twitching (hemifacial spasm) and progressive facial paralysis is more
prominent than with other tumors in the CPA.
Patients may present with cranial nerve or cerebellar dysfunction that
develops over a number of years.
Facial nerve schwannoma
Clinical findings depend on the portion of the nerve affected by the
neoplasm.
Patients can present with conductive hearing loss from middle ear
involvement, parotid mass from extratemporal involvement, or
sensorineural loss from internal auditory canal (IAC) or CPA involvement.
CPA lesions do not cause facial weakness until tumor is very large
(hemangiomas of the facial nerve usually cause symptoms at an earlier
stage).
Hemifacial spasm is relatively common.
Lower cranial nerve schwannoma
Patients may have weakness and hypesthesia of the palate, vocal cord, and
shoulder (cranial nerves [CN] IX, X, XI) or hemiatrophy of the tongue (CN
XII).
Large tumors may cause deficits of all the lower cranial nerves

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