Meningitis
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Transcript of Meningitis
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MeningitisPROBLEM BASED LEARNING (PBL)
PREPARED BY: MUHAMMAD ARIFF B. MAHDZUB
BACHELOR MEDICINE AND SURGERY (MBBS)
UNIVERSITY COLLEGE SHAHPUTRA, KUANTAN
Infectious agents reach the Nervous System through
• Hematogenous spread: through arterial blood supply.
• Direct implantation of microorganisms.
• Local extension with infections of the skull.
• Peripheral nerves: entry of pathogens such as rabies.
Meningitis
• Acute Pyogenic Meningitis (Bacterial Meningitis)
• Aseptic Meningitis (Viral Meningitis).
• Chronic Meningitis.
Acute Pyogenic Meningitis (Bacterial Meningitis)
• The organisms vary with patient age.• Neonates: Escherichia coli and group B streptococci.• Adolescents and young adults: Neisseria meningitidis.• Older individual: Streptococcus pneumoniae and Listeria
monocytogenes.• Signs: meningeal irritation and neurologic impairment
(headache, photophobia, neck stiffness).• Lumbar puncture: increase
pressure, CSF show abundant neutrophils, elevated protein and reduced glucose.
Aseptic Meningitis (Viral Meningitis).
• Patient: meningeal irritation, fever and alterations in consciousness (acute onset).
• Lumbar tap: CSF show lymphocytosis, moderate protein level, normal glucose level.
Chronic Meningitis.
• Tuberculous Meningitis.- Mycobacteria.- S&S: headache, malaise, mental confusion &
vomiting.
• Spirochetal Infections.- Neurosyphilis (tertiary stage of syphilis):
untreated Treponema pallidum infection.- S&S: progressive loss of mental and physical
functions, mood alterations and severe dementia.
Parenchymal infections.
• Brain Abscesses.
- Nearly always caused by bacterial infections.
- Arise by direct implantation of organisms, hematogenous spread.
- Patient: progressive focal deficits, general signs related to increased intracranial pressure.
• Viral Encephalitis
- Parenchymal infection of the brain that associated with meningeal inflammation.
- eg: rabies virus, poliovirus.
Prion diseases.• Agents: abnormal form of a cellular protein.
• Eg; Creutzfeldt-Jakob disease(CJD).
- A rapidly progressive dementing illness, changes in memory and behavior (death in 7 month).
TUMORS
• Gliomas – astrocytomas, oligodendrogliomas, ependymomas.
• neuronal tumors.
• Embyronal (Primitive) Neoplasms –medulloblastoma.
• Meningiomas.
• Metastatic tumors.
Epidemiology
• Primary brain tumors in adults – 70% occur above the tentorium cerebelli.
• Primary brain tumors in children – 70% occur below the tentorium cerebelli (second most common cancer in children).
• Risk factors – Turcot syndrome, neurofibromastosis, cigarette smoking.
• General clinical findings – headache, seizures.
Astrocytoma
• Accounts for about 70% of all neuroglialtumors.
• In adults – tumor usually involves frontal lobe.
• In children – tumor usually involves cerebellum.
• Low-grade cancer : Grades I and II.
• High-grade cancers: Grades III and IV.
• Rarely metastasize outside the CNS.
Oligodendroglioma
• Benign tumour derived from oligodendrocytes.
• Primarily occur in adults.
• Site of calcifies – usually frontal lobes.
Ependymoma
• Benign tumor derived from ependymal cells.
• In adults – arise in cauda equina.
• In children – arise in the fourth ventricle, can produce noncommunicating hydrocephalus.
Medulloblastoma
• Malignant small cell tumour – primarily occurs in children.
• Arises from the external granular cell layer of cerebellum.
• Often invades the fourth ventricles.
Meningiomas
• Most common benign brain tumour in adults.
• Derived from meningothelial cell within the arachnoid membrane.
• Firm tumours
- Not invade the surface of brain.
- Often infiltrate the overlying bone – caused increased bone density.