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Introduction
 There are 2 types of tissues in the nervous system:
 Neuroectodermal tissues
 which include neurons (nerve cells) and neuroglia, and
together form the predominant constituent of the CNS.
 Mesodermal tissues
 are microglia, dura mater, the leptomeninges (pia-arachnoid),
blood vessels and their accompanying mesenchymal cells.
 The predominant tissues comprising the nervous system
and their general response to injury are briefly considered
are neurons, neuroglia, microglia, dura matter and pia
arachnoid.
Introduction cont…
 Brain
Makes up 2 % (1.4 kg) of
body weight Consumes
20% of the energy.
 Three major areas: the
cerebrum, the brain stem,
and the cerebellum.
 Brain and spinal cord
covered by meninges (dura,
arachnoid, and pia mater)
which provide protection,
support, and nourishment
to the brain and spinal cord.
Developmental Anomalies
 Spinal Cord Defects
 Spina bifida: malformations of the vertebral column involving
incomplete embryologic closure of one or more of the vertebral
arches (rachischisis), most frequently in the lumbosacral region.
 Meningocele: The herniated sac in meningocele consists of dura
and arachnoid.
 meningomyelocele - spinal cord or its roots herniate through the
defect and are attached to the posterior wall of the sac.
 Hydrocephalus- increased volume of CSF within the skull,
accompanied by dilatation of the ventricles.
 internal hydrocephalus: it involving ventricular dilatation.
 external hydrocephalus: A localized collection of CSF in the
subarachnoid space
Infections
 A large number of pathogens comprising various kinds of
bacteria, fungi, viruses, rickettsiae and parasites can cause
infections of the nervous system.
 The route of causes are Via blood stream, direct implantation,
local extension and along nerve.
1. Meningitis
 is inflammatory involvement of the meninges.
 may involve the dura called pachymeningitis, or the
leptomeninges (pia-arachnoid) termed leptomeningitis.
 An extradural abscess may form by suppuration between the
bone and dura.
 Further spread of infection may penetrate the dura and form
a subdural abscess
 pachymeningitis are localised or generalised leptomeningitis
and cerebral abscess.
Meningitis cont---
A. Acute Pyogenic Meningitis
 Acute pyogenic or acute purulent meningitis is acute infection of the pia-
arachnoid and of the CSF enclosed in the subarachnoid space
 Etiopathogenesis
 Escherichia coli, Haemophilus influenzae, Neisseria meningitidis, Streptococcus
pneumoniae
 Route of causes- The blood stream, from an adjacent focus of infection and by
iatrogenic infection such as during operation or lumbar puncture.
 Morphological features
 Grossly, pus accumulates in the subarachnoid space so that normally clear CSF
becomes turbid or frankly purulent.
 Clinical Manifestations
• fever, severe headache, vomiting, drowsiness, stupor, coma, and occasionally,
convulsions
Meningitis cont---
B. Acute Lymphocytic (Viral, Aseptic) Meningitis
 etiologic agents are numerous viruses such as enteroviruses,
mumps, ECHO viruses, coxsackie virus, Epstein-Barr virus,
herpes simplex virus-2, arthropode-borne viruses and HIV
 Morphologic Features
 Grossly, some cases show swelling of the brain while others
show no distinctive change.
 The clinical manifestations of viral meningitis are much the
same as in bacterial meningitis.
 The CSF findings in viral meningitis: CSF pressure increased
(above 250 mm water)
Meningitis cont---
C. Chronic (tuberculosis and Cryptococcus) Meningitis
 Tuberculosis meningitis: hematogenous spread of infection
from tuberculosis elsewhere in the body
 Cryptococcus meningitis: occurs immunocompromised
persons via hematogenous from a pulmonary lesion.
 Morphologic features
 The subarachnoid space contains thick exudate, particularly
abundant in the sulci and the base of the brain
 CSF Finding: Raised CSF pressure (above 300 mm water).
 Clinical Manifestations: headache, confusion, malaise and
vomiting.
 The clinical course in cryptococcal meningitis may fulminant
and fatal in a few weeks, or be indolent for months to years.
Encephalitis
 It is parenchymal infection of brain.
 caused by bacterial, viral, fungal and protozoal infections.
1. Bacterial Encephalitis- bacterial cerebritis that progresses to
form brain abscess
 tuberculosis and neurosyphilis are the two primary bacterial
involvements of the brain parenchyma
 Morphologically it appears as a localised area of
inflammatory necrosis and oedema surrounded by fibrous
capsule.
 Microscopically, the changes consist of liquefactive necrosis in
the centre of the abscess containing pus.
Encephalitis cot…
 Brain abscess
Caused by
 By direct implantation of organisms e.g. following compound
fractures of the skull.
 By local extension of infection e.g. chronic supportive otitis
media, mastoiditis and sinusitis.
 hematogenous spread e.g. from primary infection in the
heart such as acute bacterial endocarditis, and from lungs
such as in bronchiectasis
 Clinical Manifestations are fever, headache, vomiting, seizures
and focal neurological deficits depending upon the location of
the abscess
Encephalitis cot…
 Tuberculoma: is an intracranial mass occurring secondary to
dissemination of tuberculosis elsewhere in the body.
 Grossly, it has a central area of caseation necrosis surrounded
by fibrous capsule.
 Microscopically, there is typical tuberculous granulomatous
reaction around the central caseation necrosis.
Cerebrovascular Diseases
 Intracranial hemorrhage
 Hemorrhage into the brain may be traumatic, non-traumatic,
or spontaneous
 Intracerebral Hemorrhage
 Spontaneous intracerebral hemorrhage occurs mostly in
patients of hypertension
 Morphologic features.
 Grossly and microscopically, the hemorrhage consists of dark
mass of clotted blood replacing brain parenchyma.
 Clinical Manifestation
 Clinically the onset is usually sudden with headache and loss
of consciousness
Cerebrovascular Diseases cont---
 Subarachnoid Hemorrhage
 Hemorrhage into the subarachnoid space is most commonly
caused by rupture of an aneurysm, and rarely, rupture of a
vascular malformation.
 In more than 85% cases of subarachnoid hemorrhage,
 the cause is massive and sudden bleeding from a berry
aneurysm on or near the circle of Willis.
 Morphologic features.
 Rupture of a berry aneurysm frequently spreads hemorrhage
throughout the subarachnoid space with rise in intracranial
pressure and characteristic blood-stained CSF.
Trauma to The CNS
1. Epidural Haematoma
• is accumulation of blood between the dura and the skull following
fracture of the skull, most commonly from rupture of middle
meningeal artery.
2. Subdural Haematoma
 is accumulation of blood between the dura and subarachnoid.
Causes of increased ICP
 Intracranial bleeding
 Increased CSF production and reduced absorption.
 Tumors inside crania
 Injury Traumatic Brain Injuries
 Hydrocephalus
 Brain Tumor
 Severe Hypertension
 Venous Sinus Thrombosis
 Restricting Jugular Venous flow
Pathophysiology
 Increased ICP from any cause decreases cerebral perfusion
 Stimulates further swelling (edema)
 Shifts brain tissue through openings in the rigid dura, resulting
in herniation, a dire, frequently fatal event.
 Decreased Cerebral Blood Flow (resulting in ischemia and cell
death)
Pathophysiology cont…
 The body’s response to a decreased CPP is to raise
 blood pressure and dilate blood vessels in the brain
– This increases cerebral blood volume
– This increases ICP
– This decreases Cerebral Perfusion Pressure (CPP)
– This causes normal body response
– This increases cerebral blood volume
– This increases ICP
– This decreases CPP
 systemic pressure rises to maintain cerebral blood flow.
Manifestation
 Changes first in LOC
 Abnormal respiratory and vasomotor responses.
 Restlessness
 Stuporous
 Comatose and exhibits abnormal motor responses
 Pupils dilated and fixed and respirations impaired, death is usually
inevitable.
Complications
• Brain stem herniation
• The patient becomes volume-overloaded
• urine output diminishes, and serum sodium concentration
becomes dilute.
• Seizure
• Stroke
• Neurological damage and death.
CNS Tumors
 Tumours of the CNS may originate in the brain or spinal cord
primary tumours, or may spread to the brain from another
primary site of cancer( metastatic tumours).
 Secondary tumor is most common
 Both benign and malignant CNS tumours are capable of
producing neurologic impairment depending upon their site.
Classification of Intracranial Tumours:
 Tumours of neuroglia (gliomas)
 Astrocytoma, oligodendroglioma, ependymoma and choroid
plexus papilloma
 Tumours of neurons
 Neuroblastoma, ganglioneuroblastoma and ganglioneuroma
 Tumours of neurons and neuroglia
 Ganglioglioma
 Medulloblastoma, neuroblastoma, pnet(primitive
neuroectodermal tumor)
 Tumours of meninges
 Meningioma and meningeal sarcoma
Classification of Intracranial Tumours cont…
 Nerve sheath tumours
 Schwannoma (neurilemmoma), neurofibroma and malignant
nerve sheath tumour
 Other primary intraparenchymal tumours
 Haemangioblastoma, primary CNS lymphoma and germ cell
tumours.
 Miscellaneous tumours
 Malignant melanoma, Craniopharyngioma, Pineal cell
tumours and Pituitary tumours
 Tumour-like lesions
 (epidermal cyst, dermoid cyst, colloid cyst)
TUMOURS OF THE CNS
General Considerations of Tumors
 Most tumors are intracranial; tumors of the spinal cord are
much less frequent.
 In adults, the majority of intracranial tumors are supratentorial.
 In children, the majority of intracranial tumors are infratentorial
i.e lower back part of brain.
 CNS tumors are the second most common form of malignancy in
children (only leukemia is more frequent).
 Primary malignant CNS tumors rarely metastasize.
 Benign intracranial tumors can result in devastating clinical
consequences due to compression phenomena.
 Metastatic tumors to the brain are found more frequently than
primary intracranial neoplasms.
General Considerations Of Tumors cont…
 the most common primary intracranial tumors in adults are
glioblastoma multiforme, meningioma, and acoustic neuroma.
 The most common primary intracranial tumors in children are
cerebellar astrocytoma and medulloblastoma.
 Gliomas
 The term glioma is used for all tumors arising from neuroglia,
or more precisely, from neuroectodermal epithelial tissue.
 Gliomas are the most common of the primary CNS tumors and
collectively account for 40% of all intracranial tumours.
 Gliomas are disseminated to other parts of the CNS by CSF
but they rarely ever metastasize beyond the CNS.
Astrocytomas
 Astrocytomas are the most common primary brain tumors.
 They can be divided based on their infiltration into the
surrounding brain parenchyma.
 Astrocytomas that do not infiltrate the brain include pilocytic
astrocytomas, pleomorphic xanthroastrocytomas,and
subependymal giant cell astrocytomas.
 Diffuse astrocytomascan be further subdivided based on grade.
 low-grade fibrillary astrocytomasare WHO grade II.
 anaplastic astrocytomasare WHO grade III.
 glioblastoma multiforme (gBM)is WHO grade IV.
CNS Tumors cont…
 Oligodendroglioma
 This neoplasm presents as a slow-growing tumor in the middle-
age group and typically arises in the cerebral hemispheres.
 Morphologic characteristics
 Closely packed cells with large round nuclei surrounded by a clear
halo of cytoplasm (“fried egg” appearance)
 Tumor divided into groups of cells by delicate capillary strands
 Foci of calcification
 Microscopically
 the tumor is characterized by uniform cells with round to oval
nuclei surrounded by a clear halo of cytoplasm and well-defined
cell membranes.
CNS Tumors Cont…
 Ependymoma
 This neoplasm most frequently occurs in the fourth ventricle.
 Peak incidence is in childhood and adolescence.
 Histologic characteristics
 Include tubules or rosettes with cells encircling vessels or
pointing toward a central lumen.
 characteristically demonstrate blepharoplasts, rod-shaped
structures near the nucleus representing basal bodies of cilia.
 Results may papillary growths that obstruct flow of CSF and lead
to hydrocephalus.
 Microscopically
 the tumour is composed of uniform epithelial (ependymal) cells
forming rosettes, canals and perivascular pseudorosettes.
CNS Tumors Cont…
 Meningioma
 This is the second most common primary intracranial neoplasm.
 Most cases are benign
 slow growing (WHO grade I) and certain subtypes show more
aggressive behavior;
 the clear cell and chordoid variants are WHO grade II and
 the papillary and rhabdoid variants are WHO grade III.
 This neoplasm most often occurs after 30 years of age. It occurs
more frequently in women than in men.
 The neoplasm originates in arachnoidal cells of the meninges; the
tumor is external to the brain and can often be successfully
removed surgically.
CNS Tumor cont…
 This neoplasm occurs most frequently in the convexities of the
cerebral hemispheres and the parasagittal region; other
common locations falxcerebri, sphenoid ridge, olfactory area,
and suprasellar region.
 Morphologic features:
 meningioma is well-circumscribed, solid, spherical or
hemispherical mass of varying size (1-10 cm in diameter).
 Histologic characteristics
a whorled pattern of concentrically arranged spindle cells and
laminated calcified psammoma bodies
CNS Tumors cont…
 Medulloblastoma
 This is one of the most common neoplasms of childhood.
 It is a highly malignant tumor of the cerebellum.
 Morphologic features:
 the tumour typically protrudes into the fourth ventricle as a soft,
greywhite mass or invades the surface of the cerebellum.
 Microscopically
is composed of small, poorly-differentiated cells with ill-defined
cytoplasmic and a tendency to be arranged around blood vessels
and occasionally forms pseudorosettes.
CNS Tumors cont…
 Neuroblastoma
 This neoplasm is closely related to neuroblastoma of the adrenal
medulla or sympathetic ganglia.
 This is much less common than peripheral neuroblastoma.
 Characteristics
 a greater degree of amplification correlates with worse prognosis.
 Hemangioblastoma
 This neoplasm occurs most frequently in the cerebellum.
 It may be associated with similar lesions in the retina and other
organs.
 It sometimes produces erythropoietin, leading to secondary
polycythemia.
CNS Tumors cont…
 Schwannoma (neurilemmoma)
 This benign, slowly growing encapsulated tumor arises from
Schwann cells.
 When intracranial, it is most frequently localized to the eighth
cranial nerve (acoustic neuroma,acoustic schwannoma);
 Acoustic neuroma is the third most common primary intracranial
neoplasm.
 It also originates frequently in posterior nerve roots and
peripheral nerves.
 Histologically
 Antoni A: interlacing bundles of elongated cells with palisading
nuclei
 Antoni B: looser, less cellular pattern than Antoni A
CNS Tumors cont…
 Metastatic tumors
 These tumors are more common than any of the primary
intracranial neoplasms.
 They originate most frequently from primary sites in lung,
breast, skin, kidney, gastrointestinal tract, and thyroid.

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pathology group assignment.pptx

  • 1. Introduction  There are 2 types of tissues in the nervous system:  Neuroectodermal tissues  which include neurons (nerve cells) and neuroglia, and together form the predominant constituent of the CNS.  Mesodermal tissues  are microglia, dura mater, the leptomeninges (pia-arachnoid), blood vessels and their accompanying mesenchymal cells.  The predominant tissues comprising the nervous system and their general response to injury are briefly considered are neurons, neuroglia, microglia, dura matter and pia arachnoid.
  • 2. Introduction cont…  Brain Makes up 2 % (1.4 kg) of body weight Consumes 20% of the energy.  Three major areas: the cerebrum, the brain stem, and the cerebellum.  Brain and spinal cord covered by meninges (dura, arachnoid, and pia mater) which provide protection, support, and nourishment to the brain and spinal cord.
  • 3. Developmental Anomalies  Spinal Cord Defects  Spina bifida: malformations of the vertebral column involving incomplete embryologic closure of one or more of the vertebral arches (rachischisis), most frequently in the lumbosacral region.  Meningocele: The herniated sac in meningocele consists of dura and arachnoid.  meningomyelocele - spinal cord or its roots herniate through the defect and are attached to the posterior wall of the sac.  Hydrocephalus- increased volume of CSF within the skull, accompanied by dilatation of the ventricles.  internal hydrocephalus: it involving ventricular dilatation.  external hydrocephalus: A localized collection of CSF in the subarachnoid space
  • 4. Infections  A large number of pathogens comprising various kinds of bacteria, fungi, viruses, rickettsiae and parasites can cause infections of the nervous system.  The route of causes are Via blood stream, direct implantation, local extension and along nerve. 1. Meningitis  is inflammatory involvement of the meninges.  may involve the dura called pachymeningitis, or the leptomeninges (pia-arachnoid) termed leptomeningitis.  An extradural abscess may form by suppuration between the bone and dura.  Further spread of infection may penetrate the dura and form a subdural abscess  pachymeningitis are localised or generalised leptomeningitis and cerebral abscess.
  • 5. Meningitis cont--- A. Acute Pyogenic Meningitis  Acute pyogenic or acute purulent meningitis is acute infection of the pia- arachnoid and of the CSF enclosed in the subarachnoid space  Etiopathogenesis  Escherichia coli, Haemophilus influenzae, Neisseria meningitidis, Streptococcus pneumoniae  Route of causes- The blood stream, from an adjacent focus of infection and by iatrogenic infection such as during operation or lumbar puncture.  Morphological features  Grossly, pus accumulates in the subarachnoid space so that normally clear CSF becomes turbid or frankly purulent.  Clinical Manifestations • fever, severe headache, vomiting, drowsiness, stupor, coma, and occasionally, convulsions
  • 6. Meningitis cont--- B. Acute Lymphocytic (Viral, Aseptic) Meningitis  etiologic agents are numerous viruses such as enteroviruses, mumps, ECHO viruses, coxsackie virus, Epstein-Barr virus, herpes simplex virus-2, arthropode-borne viruses and HIV  Morphologic Features  Grossly, some cases show swelling of the brain while others show no distinctive change.  The clinical manifestations of viral meningitis are much the same as in bacterial meningitis.  The CSF findings in viral meningitis: CSF pressure increased (above 250 mm water)
  • 7. Meningitis cont--- C. Chronic (tuberculosis and Cryptococcus) Meningitis  Tuberculosis meningitis: hematogenous spread of infection from tuberculosis elsewhere in the body  Cryptococcus meningitis: occurs immunocompromised persons via hematogenous from a pulmonary lesion.  Morphologic features  The subarachnoid space contains thick exudate, particularly abundant in the sulci and the base of the brain  CSF Finding: Raised CSF pressure (above 300 mm water).  Clinical Manifestations: headache, confusion, malaise and vomiting.  The clinical course in cryptococcal meningitis may fulminant and fatal in a few weeks, or be indolent for months to years.
  • 8. Encephalitis  It is parenchymal infection of brain.  caused by bacterial, viral, fungal and protozoal infections. 1. Bacterial Encephalitis- bacterial cerebritis that progresses to form brain abscess  tuberculosis and neurosyphilis are the two primary bacterial involvements of the brain parenchyma  Morphologically it appears as a localised area of inflammatory necrosis and oedema surrounded by fibrous capsule.  Microscopically, the changes consist of liquefactive necrosis in the centre of the abscess containing pus.
  • 9. Encephalitis cot…  Brain abscess Caused by  By direct implantation of organisms e.g. following compound fractures of the skull.  By local extension of infection e.g. chronic supportive otitis media, mastoiditis and sinusitis.  hematogenous spread e.g. from primary infection in the heart such as acute bacterial endocarditis, and from lungs such as in bronchiectasis  Clinical Manifestations are fever, headache, vomiting, seizures and focal neurological deficits depending upon the location of the abscess
  • 10. Encephalitis cot…  Tuberculoma: is an intracranial mass occurring secondary to dissemination of tuberculosis elsewhere in the body.  Grossly, it has a central area of caseation necrosis surrounded by fibrous capsule.  Microscopically, there is typical tuberculous granulomatous reaction around the central caseation necrosis.
  • 11. Cerebrovascular Diseases  Intracranial hemorrhage  Hemorrhage into the brain may be traumatic, non-traumatic, or spontaneous  Intracerebral Hemorrhage  Spontaneous intracerebral hemorrhage occurs mostly in patients of hypertension  Morphologic features.  Grossly and microscopically, the hemorrhage consists of dark mass of clotted blood replacing brain parenchyma.  Clinical Manifestation  Clinically the onset is usually sudden with headache and loss of consciousness
  • 12. Cerebrovascular Diseases cont---  Subarachnoid Hemorrhage  Hemorrhage into the subarachnoid space is most commonly caused by rupture of an aneurysm, and rarely, rupture of a vascular malformation.  In more than 85% cases of subarachnoid hemorrhage,  the cause is massive and sudden bleeding from a berry aneurysm on or near the circle of Willis.  Morphologic features.  Rupture of a berry aneurysm frequently spreads hemorrhage throughout the subarachnoid space with rise in intracranial pressure and characteristic blood-stained CSF.
  • 13. Trauma to The CNS 1. Epidural Haematoma • is accumulation of blood between the dura and the skull following fracture of the skull, most commonly from rupture of middle meningeal artery. 2. Subdural Haematoma  is accumulation of blood between the dura and subarachnoid.
  • 14. Causes of increased ICP  Intracranial bleeding  Increased CSF production and reduced absorption.  Tumors inside crania  Injury Traumatic Brain Injuries  Hydrocephalus  Brain Tumor  Severe Hypertension  Venous Sinus Thrombosis  Restricting Jugular Venous flow
  • 15. Pathophysiology  Increased ICP from any cause decreases cerebral perfusion  Stimulates further swelling (edema)  Shifts brain tissue through openings in the rigid dura, resulting in herniation, a dire, frequently fatal event.  Decreased Cerebral Blood Flow (resulting in ischemia and cell death)
  • 16. Pathophysiology cont…  The body’s response to a decreased CPP is to raise  blood pressure and dilate blood vessels in the brain – This increases cerebral blood volume – This increases ICP – This decreases Cerebral Perfusion Pressure (CPP) – This causes normal body response – This increases cerebral blood volume – This increases ICP – This decreases CPP  systemic pressure rises to maintain cerebral blood flow.
  • 17. Manifestation  Changes first in LOC  Abnormal respiratory and vasomotor responses.  Restlessness  Stuporous  Comatose and exhibits abnormal motor responses  Pupils dilated and fixed and respirations impaired, death is usually inevitable.
  • 18. Complications • Brain stem herniation • The patient becomes volume-overloaded • urine output diminishes, and serum sodium concentration becomes dilute. • Seizure • Stroke • Neurological damage and death.
  • 19. CNS Tumors  Tumours of the CNS may originate in the brain or spinal cord primary tumours, or may spread to the brain from another primary site of cancer( metastatic tumours).  Secondary tumor is most common  Both benign and malignant CNS tumours are capable of producing neurologic impairment depending upon their site.
  • 20. Classification of Intracranial Tumours:  Tumours of neuroglia (gliomas)  Astrocytoma, oligodendroglioma, ependymoma and choroid plexus papilloma  Tumours of neurons  Neuroblastoma, ganglioneuroblastoma and ganglioneuroma  Tumours of neurons and neuroglia  Ganglioglioma  Medulloblastoma, neuroblastoma, pnet(primitive neuroectodermal tumor)  Tumours of meninges  Meningioma and meningeal sarcoma
  • 21. Classification of Intracranial Tumours cont…  Nerve sheath tumours  Schwannoma (neurilemmoma), neurofibroma and malignant nerve sheath tumour  Other primary intraparenchymal tumours  Haemangioblastoma, primary CNS lymphoma and germ cell tumours.  Miscellaneous tumours  Malignant melanoma, Craniopharyngioma, Pineal cell tumours and Pituitary tumours  Tumour-like lesions  (epidermal cyst, dermoid cyst, colloid cyst)
  • 23. General Considerations of Tumors  Most tumors are intracranial; tumors of the spinal cord are much less frequent.  In adults, the majority of intracranial tumors are supratentorial.  In children, the majority of intracranial tumors are infratentorial i.e lower back part of brain.  CNS tumors are the second most common form of malignancy in children (only leukemia is more frequent).  Primary malignant CNS tumors rarely metastasize.  Benign intracranial tumors can result in devastating clinical consequences due to compression phenomena.  Metastatic tumors to the brain are found more frequently than primary intracranial neoplasms.
  • 24. General Considerations Of Tumors cont…  the most common primary intracranial tumors in adults are glioblastoma multiforme, meningioma, and acoustic neuroma.  The most common primary intracranial tumors in children are cerebellar astrocytoma and medulloblastoma.  Gliomas  The term glioma is used for all tumors arising from neuroglia, or more precisely, from neuroectodermal epithelial tissue.  Gliomas are the most common of the primary CNS tumors and collectively account for 40% of all intracranial tumours.  Gliomas are disseminated to other parts of the CNS by CSF but they rarely ever metastasize beyond the CNS.
  • 25. Astrocytomas  Astrocytomas are the most common primary brain tumors.  They can be divided based on their infiltration into the surrounding brain parenchyma.  Astrocytomas that do not infiltrate the brain include pilocytic astrocytomas, pleomorphic xanthroastrocytomas,and subependymal giant cell astrocytomas.  Diffuse astrocytomascan be further subdivided based on grade.  low-grade fibrillary astrocytomasare WHO grade II.  anaplastic astrocytomasare WHO grade III.  glioblastoma multiforme (gBM)is WHO grade IV.
  • 26.
  • 27. CNS Tumors cont…  Oligodendroglioma  This neoplasm presents as a slow-growing tumor in the middle- age group and typically arises in the cerebral hemispheres.  Morphologic characteristics  Closely packed cells with large round nuclei surrounded by a clear halo of cytoplasm (“fried egg” appearance)  Tumor divided into groups of cells by delicate capillary strands  Foci of calcification  Microscopically  the tumor is characterized by uniform cells with round to oval nuclei surrounded by a clear halo of cytoplasm and well-defined cell membranes.
  • 28. CNS Tumors Cont…  Ependymoma  This neoplasm most frequently occurs in the fourth ventricle.  Peak incidence is in childhood and adolescence.  Histologic characteristics  Include tubules or rosettes with cells encircling vessels or pointing toward a central lumen.  characteristically demonstrate blepharoplasts, rod-shaped structures near the nucleus representing basal bodies of cilia.  Results may papillary growths that obstruct flow of CSF and lead to hydrocephalus.  Microscopically  the tumour is composed of uniform epithelial (ependymal) cells forming rosettes, canals and perivascular pseudorosettes.
  • 29. CNS Tumors Cont…  Meningioma  This is the second most common primary intracranial neoplasm.  Most cases are benign  slow growing (WHO grade I) and certain subtypes show more aggressive behavior;  the clear cell and chordoid variants are WHO grade II and  the papillary and rhabdoid variants are WHO grade III.  This neoplasm most often occurs after 30 years of age. It occurs more frequently in women than in men.  The neoplasm originates in arachnoidal cells of the meninges; the tumor is external to the brain and can often be successfully removed surgically.
  • 30. CNS Tumor cont…  This neoplasm occurs most frequently in the convexities of the cerebral hemispheres and the parasagittal region; other common locations falxcerebri, sphenoid ridge, olfactory area, and suprasellar region.  Morphologic features:  meningioma is well-circumscribed, solid, spherical or hemispherical mass of varying size (1-10 cm in diameter).  Histologic characteristics a whorled pattern of concentrically arranged spindle cells and laminated calcified psammoma bodies
  • 31. CNS Tumors cont…  Medulloblastoma  This is one of the most common neoplasms of childhood.  It is a highly malignant tumor of the cerebellum.  Morphologic features:  the tumour typically protrudes into the fourth ventricle as a soft, greywhite mass or invades the surface of the cerebellum.  Microscopically is composed of small, poorly-differentiated cells with ill-defined cytoplasmic and a tendency to be arranged around blood vessels and occasionally forms pseudorosettes.
  • 32. CNS Tumors cont…  Neuroblastoma  This neoplasm is closely related to neuroblastoma of the adrenal medulla or sympathetic ganglia.  This is much less common than peripheral neuroblastoma.  Characteristics  a greater degree of amplification correlates with worse prognosis.  Hemangioblastoma  This neoplasm occurs most frequently in the cerebellum.  It may be associated with similar lesions in the retina and other organs.  It sometimes produces erythropoietin, leading to secondary polycythemia.
  • 33. CNS Tumors cont…  Schwannoma (neurilemmoma)  This benign, slowly growing encapsulated tumor arises from Schwann cells.  When intracranial, it is most frequently localized to the eighth cranial nerve (acoustic neuroma,acoustic schwannoma);  Acoustic neuroma is the third most common primary intracranial neoplasm.  It also originates frequently in posterior nerve roots and peripheral nerves.  Histologically  Antoni A: interlacing bundles of elongated cells with palisading nuclei  Antoni B: looser, less cellular pattern than Antoni A
  • 34. CNS Tumors cont…  Metastatic tumors  These tumors are more common than any of the primary intracranial neoplasms.  They originate most frequently from primary sites in lung, breast, skin, kidney, gastrointestinal tract, and thyroid.