Medulloblastoma history and symptoms: Difference between revisions
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{{Medulloblastoma}} | {{Medulloblastoma}} | ||
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==Overview== | |||
==History and Symptoms== | ==History and Symptoms== | ||
Symptoms are mainly due to secondary increased [[intracranial pressure]] due to blockage of the [[fourth ventricle]] and are usually present for 1 to 5 months before diagnosis is made. The child typically becomes ''listless'', with repeated episodes of ''vomiting'', and a ''morning headache'', which may lead to a misdiagnosis of gastrointestinal disease or migraine. Soon, the child will develop a ''stumbling gait'', ''frequent falls'', ''[[diplopia]]'', ''[[papilledema]]'', and ''sixth cranial nerve palsy''. ''Positional dizziness'' and ''[[nystagmus]]'' are also frequent and facial sensory loss or motor weakness may be present. [[Decerebrate]] attacks appear late in the disease. | Symptoms are mainly due to secondary increased [[intracranial pressure]] due to blockage of the [[fourth ventricle]] and are usually present for 1 to 5 months before diagnosis is made. The child typically becomes ''listless'', with repeated episodes of ''vomiting'', and a ''morning headache'', which may lead to a misdiagnosis of gastrointestinal disease or migraine. Soon, the child will develop a ''stumbling gait'', ''frequent falls'', ''[[diplopia]]'', ''[[papilledema]]'', and ''sixth cranial nerve palsy''. ''Positional dizziness'' and ''[[nystagmus]]'' are also frequent and facial sensory loss or motor weakness may be present. [[Decerebrate]] attacks appear late in the disease. |
Revision as of 18:10, 13 September 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
History and Symptoms
Symptoms are mainly due to secondary increased intracranial pressure due to blockage of the fourth ventricle and are usually present for 1 to 5 months before diagnosis is made. The child typically becomes listless, with repeated episodes of vomiting, and a morning headache, which may lead to a misdiagnosis of gastrointestinal disease or migraine. Soon, the child will develop a stumbling gait, frequent falls, diplopia, papilledema, and sixth cranial nerve palsy. Positional dizziness and nystagmus are also frequent and facial sensory loss or motor weakness may be present. Decerebrate attacks appear late in the disease.
Extraneural metastases to the rest of the body is rare, but usually only after craniotomy.