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[[Image:Pilocytic astrocytoma 1.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. As illustrated, many lesions are composed largely of spongy tissue rich in microcysts. Characteristic of [[pilocytic astrocytoma]]s in general, the lesion is largely a solid mass of neoplastic cells without an obvious background of infiltrated brain.|250px]]
[[Image:Pilocytic astrocytoma 1.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. As illustrated, many lesions are composed largely of spongy tissue rich in microcysts. Characteristic of [[pilocytic astrocytoma]]s in general, the lesion is largely a solid mass of neoplastic cells without an obvious background of infiltrated brain.|250px]]
[[Image:Pilocytic astrocytoma 2.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. The perivascular radiating processes in some lesions can create a likeness to an [[ependymoma]]. Note the spongy background unusual for [[ependymoma]]s.|250px]]
[[Image:Pilocytic astrocytoma 2.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. The perivascular radiating processes in some lesions can create a likeness to an [[ependymoma]]. Note the spongy background unusual for [[ependymoma]]s.|250px]]
[[Image:Pilocytic astrocytoma 3.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Other [[pilocytic astrocytoma]]s are solid, rather than microcystic, and may be lobular.|250px]]
[[Image:Pilocytic astrocytoma 3.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Other [[pilocytic astrocytoma]]s are solid, rather than microcystic, and may be lobular.|250px]]
[[Image:Pilocytic astrocytoma 4.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Rosenthal fibers, usually confined to the solid rather than spongy regions are found in many pilocytic [[astrocytoma]]s, but are not requisite for the diagnosis.|250px]]
[[Image:Pilocytic astrocytoma 4.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Rosenthal fibers, usually confined to the solid rather than spongy regions are found in many pilocytic [[astrocytoma]]s, but are not requisite for the diagnosis.|250px]]
[[Image:Pilocytic astrocytoma 15.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Rosenthal fibers are extremely abundant in some lesions. Particularly in the [[cerebellum]], it can be difficult to distinguish such solid, paucicellular, highly fibrillar [[pilocytic astrocytoma]]s from reactive gliosis with abundant Rosenthal fiber formation.|250px]]
[[Image:Pilocytic astrocytoma 15.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Rosenthal fibers are extremely abundant in some lesions. Particularly in the [[cerebellum]], it can be difficult to distinguish such solid, paucicellular, highly fibrillar [[pilocytic astrocytoma]]s from reactive gliosis with abundant Rosenthal fiber formation.|250px]]
[[Image:Pilocytic astrocytoma 16.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. A loose array of polar cells creates an additional variant of pilocytic [[astrocytoma]].|250px]]
[[Image:Pilocytic astrocytoma 16.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. A loose array of polar cells creates an additional variant of pilocytic [[astrocytoma]].|250px]]
[[Image:Pilocytic astrocytoma 7.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Some pilocytic [[astrocytoma]]s are traversed by prominent collagenous septa.|250px]]
[[Image:Pilocytic astrocytoma 7.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Some pilocytic [[astrocytoma]]s are traversed by prominent collagenous septa.|250px]]
[[Image:Pilocytic astrocytoma 8.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Unusual pilocytic [[astrocytoma]]s have an extensive mucinous background without microcysts.|250px]]
[[Image:Pilocytic astrocytoma 8.jpg|CNS: [[Pilocytic astrocytoma]]: variations in histologic appearance. Unusual pilocytic [[astrocytoma]]s have an extensive mucinous background without microcysts.|250px]]
[[Image:Comparison.jpg|CNS: Comparison of normal [[optic nerve]] and [[pilocytic astrocytoma]] of the [[optic nerve]]. These two figures compare, at the same magnification, the normal [[optic nerve]] (left) with one containing a [[pilocytic astrocytoma]] (right). The [[neoplasm]] enlarges the compartments of the [[nerve]] and extends in collar-like fashion into the [[subarachnoid]] space.|250px]]
[[Image:Comparison.jpg|CNS: Comparison of normal [[optic nerve]] and [[pilocytic astrocytoma]] of the [[optic nerve]]. These two figures compare, at the same magnification, the normal [[optic nerve]] (left) with one containing a [[pilocytic astrocytoma]] (right). The [[neoplasm]] enlarges the compartments of the [[nerve]] and extends in collar-like fashion into the [[subarachnoid]] space.|250px]]
[[Image:Pilocytic astrocytoma 9.jpg|CNS: [[Pilocytic astrocytoma]]; The "hair cells" for which this lesion is named are readily seen.|250px]]
[[Image:Pilocytic astrocytoma 9.jpg|CNS: [[Pilocytic astrocytoma]]; The "hair cells" for which this lesion is named are readily seen.|250px]]
[[Image:Pilocytic astrocytoma 10.jpg|CNS: [[Pilocytic astrocytoma]]; Nuclear hyperchromasia and [[pleomorphism]] are common. Note the typical cellular elongation, and, at the center of the illustration, the [[eosinophil]]ic granular body that populates [[pilocytic astrocytoma]]s and certain other slowly growing gliomas.|250px]]
[[Image:Pilocytic astrocytoma 10.jpg|CNS: [[Pilocytic astrocytoma]]; Nuclear hyperchromasia and [[pleomorphism]] are common. Note the typical cellular elongation, and, at the center of the illustration, the [[eosinophil]]ic granular body that populates [[pilocytic astrocytoma]]s and certain other slowly growing gliomas.|250px]]
[[Image:Pilocytic astrocytoma 11.jpg|CNS: [[Pilocytic astrocytoma]]; Intracytoplasmic Rosenthal fibers are prominent in some pilocytic [[neoplasm]]s.|250px]]
[[Image:Pilocytic astrocytoma 11.jpg|CNS: [[Pilocytic astrocytoma]]; Intracytoplasmic Rosenthal fibers are prominent in some pilocytic [[neoplasm]]s.|250px]]
[[Image:Malignant ependymoma.jpg|Brain: [[Malignant]] [[ependymoma]]: Micro med mag H&E tumor cells.|250px]]
[[Image:Malignant ependymoma.jpg|Brain: [[Malignant]] [[ependymoma]]: Micro med mag H&E tumor cells.|250px]]
[[Image:Oligodendroglioma 2.jpg|CNS: [[Oligodendroglioma]]; Occasional [[oligodendroglioma]]s contain cells with minute, refractile [[eosinophil]]ic bodies representing miniature Rosenthal fibers.|250px]]
[[Image:Oligodendroglioma 2.jpg|CNS: [[Oligodendroglioma]]; Occasional [[oligodendroglioma]]s contain cells with minute, refractile [[eosinophil]]ic bodies representing miniature Rosenthal fibers.|250px]]
[[Image:Oligodendroglioma 1.jpg|CNS: [[Oligodendroglioma]]; The cells of some [[oligodendroglioma]]s acquire sufficient [[cytoplasm]] and process formation to become decidedly astrocytic, but their nuclei retain the roundness, uniformity, and chromatin distribution typical of [[oligodendroglioma]].|250px]]
[[Image:Oligodendroglioma 1.jpg|CNS: [[Oligodendroglioma]]; The cells of some [[oligodendroglioma]]s acquire sufficient [[cytoplasm]] and process formation to become decidedly astrocytic, but their nuclei retain the roundness, uniformity, and chromatin distribution typical of [[oligodendroglioma]].|250px]]
[[Image:Anaplastic oligodendroglioma.jpg|[[Anaplastic]] [[oligodendroglioma]]: [[Anaplastic]] [[oligodendroglioma]]s are highly cellular and associated with vascular proliferation.|250px]]
[[Image:Anaplastic oligodendroglioma.jpg|[[Anaplastic]] [[oligodendroglioma]]: [[Anaplastic]] [[oligodendroglioma]]s are highly cellular and associated with vascular proliferation.|250px]]
[[Image:Oligodendroglioma frozen.jpg|CNS: [[Oligodendroglioma]] (frozen section); [[Oligodendroglioma]]s in frozen sections lack the distinctive halos so often seen in permanent sections. Cellular monomorphism and infiltration of [[cerebral cortex]] with perineuronal satellitosis suggest the correct diagnosis.|250px]]
[[Image:Oligodendroglioma frozen.jpg|CNS: [[Oligodendroglioma]] (frozen section); [[Oligodendroglioma]]s in frozen sections lack the distinctive halos so often seen in permanent sections. Cellular monomorphism and infiltration of [[cerebral cortex]] with perineuronal satellitosis suggest the correct diagnosis.|250px]]
[[Image:Clear cell ependymoma.jpg|CNS: Clear cell [[ependymoma]]; Perinuclear clearing similar to that seen in [[oligodendroglioma]]s is a prominent feature of the clear cell variant. Note the vague perivascular pseudorosettes. The lesion was a discrete occipital intraventricular mass.|250px]]
[[Image:Clear cell ependymoma.jpg|CNS: Clear cell [[ependymoma]]; Perinuclear clearing similar to that seen in [[oligodendroglioma]]s is a prominent feature of the clear cell variant. Note the vague perivascular pseudorosettes. The lesion was a discrete occipital intraventricular mass.|250px]]
[[Image:Glioblastoma multiforme 1.jpg|CNS: [[Glioblastoma multiforme]]; Brain: [[Glioblastoma multiforme]]. Grade I-Ii: Micro med mag with H&E, [[tumor]] well shown|250px]]
[[Image:Glioblastoma multiforme 1.jpg|CNS: [[Glioblastoma multiforme]]; Brain: [[Glioblastoma multiforme]]. Grade I-Ii: Micro med mag with H&E, [[tumor]] well shown|250px]]
[[Image:Glioblastoma multiforme 2.jpg|CNS: [[Glioblastoma multiforme]] arising in an [[astrocytoma]]. At higher magnification, gemistocytic [[astrocytoma]] with microcystic change is apparent at the bottom of the illustration and cellular nodules of [[glioblastoma multiforme]] are seen at the top. The 6-year history of symptoms attested to the initially low-grade nature of this astrocytic tumor.|250px]]
[[Image:Glioblastoma multiforme 2.jpg|CNS: [[Glioblastoma multiforme]] arising in an [[astrocytoma]]. At higher magnification, gemistocytic [[astrocytoma]] with microcystic change is apparent at the bottom of the illustration and cellular nodules of [[glioblastoma multiforme]] are seen at the top. The 6-year history of symptoms attested to the initially low-grade nature of this astrocytic tumor.|250px]]
[[Image:Glioblastoma multiforme 103.jpg|CNS: [[Glioblastoma multiforme]]; Characteristic of most [[glioblastoma]]s are small cells with elongated nuclei and bipolar processes. As here, the [[chromatin]] is generally not markedly dense nor are nucleoli usually prominent.|250px]]
[[Image:Glioblastoma multiforme 103.jpg|CNS: [[Glioblastoma multiforme]]; Characteristic of most [[glioblastoma]]s are small cells with elongated nuclei and bipolar processes. As here, the [[chromatin]] is generally not markedly dense nor are nucleoli usually prominent.|250px]]
[[Image:Glioblastoma multiforme 104.jpg|CNS: [[Glioblastoma multiforme]]; Vascular proliferation, a common feature of glioblastoma, produces tufts which often grow directionally. Here, as is often the case, they are oriented toward a focus of necrosis (top right).|250px]]
[[Image:Glioblastoma multiforme 104.jpg|CNS: [[Glioblastoma multiforme]]; Vascular proliferation, a common feature of glioblastoma, produces tufts which often grow directionally. Here, as is often the case, they are oriented toward a focus of necrosis (top right).|250px]]
[[Image:Glioblastoma multiforme 105.jpg|CNS: [[Glioblastoma multiforme]]; At high magnification, the neovascular tuft is a mass which, as can be confirmed by immunohistochemistry, is formed of both endothelial cells and smooth muscle cells (pericytes).|250px]]
[[Image:Glioblastoma multiforme 105.jpg|CNS: [[Glioblastoma multiforme]]; At high magnification, the neovascular tuft is a mass which, as can be confirmed by immunohistochemistry, is formed of both endothelial cells and smooth muscle cells (pericytes).|250px]]
[[Image:Glioblastoma multiforme 106.jpg|CNS: [[Glioblastoma multiforme]]; In many instances, [[necrosis]] is surrounded by a distinctive collar of cells, which are often smaller than those in surrounding neoplastic tissue. The phenomenon is referred to as pseudopalisading.|250px]]
[[Image:Glioblastoma multiforme 106.jpg|CNS: [[Glioblastoma multiforme]]; In many instances, [[necrosis]] is surrounded by a distinctive collar of cells, which are often smaller than those in surrounding neoplastic tissue. The phenomenon is referred to as pseudopalisading.|250px]]
[[Image:Cerebrospinal dissemination of glioblastoma multiforme 1.jpg|CNS: Cerebrospinal dissemination of glioblastoma multiforme; As seen at low (left) and high (right) magnification, the small undifferentiated-appearing cells of this glioblastoma are drop metastases colonizing the nerve roots of the cauda equina.|250px]]
[[Image:Cerebrospinal dissemination of glioblastoma multiforme 1.jpg|CNS: Cerebrospinal dissemination of glioblastoma multiforme; As seen at low (left) and high (right) magnification, the small undifferentiated-appearing cells of this glioblastoma are drop metastases colonizing the nerve roots of the cauda equina.|250px]]
[[Image:Cerebrospinal dissemination of glioblastoma multiforme 2.jpg|CNS: Cerebrospinal dissemination of glioblastoma multiforme; As seen at low (left) and high (right) magnification, the small undifferentiated-appearing cells of this glioblastoma are drop metastases colonizing the nerve roots of the cauda equina.|250px]]
[[Image:Cerebrospinal dissemination of glioblastoma multiforme 2.jpg|CNS: Cerebrospinal dissemination of glioblastoma multiforme; As seen at low (left) and high (right) magnification, the small undifferentiated-appearing cells of this glioblastoma are drop metastases colonizing the nerve roots of the cauda equina.|250px]]
[[Image:Glioblastoma multiforme 116.jpg|CNS: [[Glioblastoma multiforme]]; Higher magnification reveals the small cell nature of such tumors.|250px]]
[[Image:Glioblastoma multiforme 116.jpg|CNS: [[Glioblastoma multiforme]]; Higher magnification reveals the small cell nature of such tumors.|250px]]
[[Image:Glioblastoma multiforme 117.jpg|CNS: [[Glioblastoma multiforme]]; Some glioblastomas are especially infiltrative of the cerebral cortex where subpial, perivascular, and perineuronal accumulations are prominent.|250px]]
[[Image:Glioblastoma multiforme 117.jpg|CNS: [[Glioblastoma multiforme]]; Some glioblastomas are especially infiltrative of the cerebral cortex where subpial, perivascular, and perineuronal accumulations are prominent.|250px]]
[[Image:Glioblastoma multiforme 126.jpg|CNS: [[Glioblastoma multiforme]]; Although this densely cellular and largely undifferentiated lesion technically merits a diagnosis of [[anaplastic]] [[astrocytoma]], it is, for practical purposes, a glioblastoma.|250px]]
[[Image:Glioblastoma multiforme 126.jpg|CNS: [[Glioblastoma multiforme]]; Although this densely cellular and largely undifferentiated lesion technically merits a diagnosis of [[anaplastic]] [[astrocytoma]], it is, for practical purposes, a glioblastoma.|250px]]
[[Image:Glioblastoma multiforme malignant astrocytoma 1.jpg|Brain: [[Glioblastoma multiforme]] [[malignant]] [[astrocytoma]]|250px]]
[[Image:Glioblastoma multiforme malignant astrocytoma 1.jpg|Brain: [[Glioblastoma multiforme]] [[malignant]] [[astrocytoma]]|250px]]
[[Image:Glioblastoma multiforme pallisading.jpg|Brain: [[Glioblastoma multiforme]]; pallisading|250px]]
[[Image:Glioblastoma multiforme pallisading.jpg|Brain: [[Glioblastoma multiforme]]; pallisading|250px]]
[[Image:Glioblastoma multiforme vascular proliferation.jpg|Brain: [[Glioblastoma multiforme]]; vascular proliferation|250px]]
[[Image:Glioblastoma multiforme vascular proliferation.jpg|Brain: [[Glioblastoma multiforme]]; vascular proliferation|250px]]
[[Image:Glioblastoma multiforme extravasated blood.jpg|Brain: [[Glioblastoma multiforme]]; Plump and juicy [[endothelial cell]]s, extravasated blood|250px]]
[[Image:Glioblastoma multiforme extravasated blood.jpg|Brain: [[Glioblastoma multiforme]]; Plump and juicy [[endothelial cell]]s, extravasated blood|250px]]
[[Image:Glioblastoma multiforme perivascular lymphocytes.jpg|Brain: [[Glioblastoma multiforme]]; perivascular [[lymphocyte]]s|250px]]
[[Image:Glioblastoma multiforme perivascular lymphocytes.jpg|Brain: [[Glioblastoma multiforme]]; perivascular [[lymphocyte]]s|250px]]
[[Image:Glioblastoma multiforme thrombosed vessel.jpg|Brain: [[Glioblastoma multiforme]]; thrombosed vessel|250px]]
[[Image:Glioblastoma multiforme thrombosed vessel.jpg|Brain: [[Glioblastoma multiforme]]; thrombosed vessel|250px]]
[[Image:Hemosiderin in glioblastoma.jpg|Brain: [[Glioblastoma multiforme]]; [[Hemosiderin]] in glioblastoma|250px]]
[[Image:Hemosiderin in glioblastoma.jpg|Brain: [[Glioblastoma multiforme]]; [[Hemosiderin]] in glioblastoma|250px]]

Revision as of 17:47, 23 September 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2], Sujit Routray, M.D. [3]

Overview

Pathogenesis of glioma involves astrocytes, members of the glial family. The hallmark of the pathology of cerebral gliomas is invasion of the astrocytes into the adjacent normal brain. Although in certain areas the margin of the tumor may seem to be macroscopically well defined from the brain, there are always microscopic nests of tumor cells extending well out into the brain.[1] Genes involved in the pathogenesis of glioma include ERCC1, ERCC2, XRCC1, MGMT, IDH1, IDH2, p53, EGFR, TSC1, TSC2, RB1, APC, hMLH1, hMSH2, PMS2, PTEN, NF1, and NF2.[2][3] The gross and microscopic histopathological appearance of glioma varies with the tumor grade.

Pathophysiology

Pathogenesis

  • Pathogenesis of glioma involves astrocytes, members of the glial family.
  • The hallmark of the pathology of cerebral gliomas is invasion of the astrocytes into the adjacent normal brain. Although in certain areas the margin of the tumor may seem to be macroscopically well defined from the brain, there are always microscopic nests of tumor cells extending well out into the brain.[1]
  • Astrocytic projections interact with vessels and act as additional elements of the blood brain barrier (BBB). The tumors take advantage of the blood brain barrier to ensure survival and continuous growth.
  • Glioma cells migrate to different regions of the brain guided by the extension of blood vessels, colonizing the healthy adjacent tissue.
  • Uncontrolled and fast growth also leads to the disruption of the chimeric and fragile vessels in the tumor mass resulting in peritumoral edema.[4]

Genetics

Genes involved in the pathogenesis of glioma include:[2][3]

Associated Conditions

Gliomas may be associated with:[3][1]

Gross Pathology

The gross pathological appearance of glioma varies with the tumor grade.[5] Common findings are listed below:

Type of glioma Gross pathological features

Pilocytic astrocytoma

1. Well-circumscribed cystic tumor
2. Solid mural nodule
3. Commonly located in the cerebellum

Low-grade astrocytoma

1. Poorly demarcated tumor
2. Tumor mass causing enlargement of the involved portion of the brain and blurring of anatomical landmarks
3. Commonly located in the cerebral hemisphere

Anaplastic astrocytoma

1. Spongy or gelationous mass
2. Ill defined borders
3. Microcysts
4. Calcification
5. Commonly located in frontal lobe, temporal lobe, brain stem, or spinal cord

Glioblastoma multiforme

1. Poorly-marginated, diffusely infiltrating tumor
2. Firm or gelatinous in consistency
3. Central necrotic core
4. Commonly located in the frontal and temporal lobe

Oligodendroglioma

1. Well circumscribed tumor
2. Pinkish-white in color
3. Mucinous changes
4. Commonly located in the frontal lobe, followed by parietal and temporal lobes

Ependymoma

1. Well-differentiated tumor
2. Exophytic pattern of growth
3. Commonly located at the fourth ventricle and filum terminale


Images shown below are courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology

Brain: Pontine Glioma: Gross; fixed tissue, anterior view of brain stem and cerebellum with bosselated tumor adjacent to basilar artery Brain: Pontine Glioma: Gross; fixed tissue, sagittal section brain stem and cerebellum Brain: Glioma: Gross; fixed tissue, horizontal section brain stem and cerebellum with obvious gelatinous appearing neoplasm a pontine glioma Brain: Oligodendroglioma: Gross; natural color, large, well circumscribed lesion in left frontal lobe Brain: Glioma: Gross; fixed tissue, horizontal sections brain stem and cerebellum showing large pontine glioma Brain: Pontine Glioma and Diffuse Meningeal Gliomatosis: Gross; fixed tissue, view of cerebral hemispheres from inferior with brain stem and cerebellum removed. Pontine asymmetry is easily seen due to low grade astrocytoma and meningeal gliomatosis is easily seen over frontal lobe Brain: Pontine Glioma and Diffuse Meningeal Gliomatosis in 7 yo boy: Gross; fixed tissue, view of cerebral hemispheres from vertex meningeal gliomatosis Brain: Pontine Glioma and Diffuse Meningeal Gliomatosis: Gross; in situ dural nodule Brain: Oligodendroglioma: Gross; fixed tissue, multiple coronal sections, cerebral hemispheres with large tumor and hemorrhage into tumor Brain: Oligodendroglioma: Gross; fixed tissue, coronal section, cerebral hemispheres, large hemorrhagic lesion in one hemisphere Brain: Oligodendroglioma: Gross; fixed tissue, ischemic tissue, anterior to tumor mass Brain: Oligodendroglioma: Gross; natural color, coronal section, cerebral hemispheres, large lesion, left parieto occipital white matter Brain: Gliomatosis Cerebri: Gross; fixed tissue, coronal sections, cerebral hemispheres, lesion is in temporal lobes and hypothalamus Brain: Ventriculitis: Gross; fixed tissue, case of glioma with meningitis, a nice view of ventriculitis in one lateral ventricle Brain: Glioma Thalamic Grade Ii-Iii: Gross; fixed tissue, four coronal sections, cerebral hemispheres, very large hemorrhagic lesion Brain: Glioma Thalamic Grade Ii-Iii: Gross; fixed tissue, coronal section, cerebral hemispheres with large hemorrhagic lesion Brain: Glioma Thalamic Grade Ii-Iii: Gross fixed tissue coronal section cerebral hemispheres lesions appears to be in choroid plexus of lateral ventricle in this picture. There is blood in fourth ventricle Brain: Cerebral Sarcoma or Microglioma: Gross; fixed tissue, coronal section, cerebral hemispheres (58 yo man) Brain: Cerebral Sarcoma or Microglioma: Gross; fixed tissue, coronal section, cerebral hemispheres Brain: Cerebral Sarcoma or Microglioma: Gross; fixed tissue, coronal section, cerebral hemispheres Brain: Infarct Subcortical: Gross; fixed tissue, close-up view of old small subcortical infarct, a case of microglioma Brain: Microglioma: Gross; fixed tissue; cerebellum and fourth ventricle with periventricular tumor invasion Brain: Microglioma: Gross fixed tissue horizontal sections cerebellum and brain stem with periventricular neoplastic infiltrate Brain: Microglioma: Gross fixed tissue horizontal section midbrain and cerebellum at mid pons level periventricular tumor infiltration Brain: Microglioma: Gross fixed tissue horizontal section rostral pons and cerebellum Brain: Microglioma: Gross fixed tissue horizontal section rostral pons and cerebellum periventricular tumor invasion Brain: Microglioma: Gross fixed tissue coronal section cerebral hemispheres with mild ventricular dilation Glioma: Optic Nerve Brain: Oligodendroglioma, Frontal Lobe Brain: Oligodendroglioma, Mixed Astrocytoma & Oligodendroglioma Brain: Oligodendroglioma Brain: Oligodendroglioma Brain: Glioma, Grade II Anaplastic Brain: Glioma, Brain stem, Low Grade Fundoscopy: Eye; Optic nerve glioma, Optic nerve Brain: Glioma, hypothalamic, Circle around region of tumor CNS: Pilocytic Astrocytoma of the Spinal Cord. The fusiform expansion of the spinal cord produced by this pilocytic astrocytoma is not, on external examination alone, distinguishable from that produced by a nonresectable diffuse glioma. Brain: Glioma, Pontine Brain: Glioblastoma Multiforme: Gross fixed tissue close-up large necrotic tumor mass in septum pellucidum Brain: Glioblastoma Multiforme: Gross fixed tissue coronal section of the brain with a large necrotic tumor mass in septum pellucidum diagnosed as astrocytoma grade III Brain: Glioblastoma Multiforme: Gross natural color large hemorrhagic lesion in right centrum semiovale CNS: Malignant pilocytic astrocytoma: A 29-year-old woman died 2 years after a diagnosis of "atypical pilocytic astrocytoma" of the pineal region. At autopsy, multiple tumor implants were present in the craniospinal subarachnoid spaces. Brain: Oligodendroglioma; Ventricular Cobblestone Effect

Microscopic Pathology

The histopathological appearance of glioma varies with the tumor grade, with increasing cellular atypia, mitoses, endothelial and adventitial cell proliferation and necrosis with increasing grade of the tumor.[5] Common findings are listed below:

Type of glioma Histopathological features

Pilocytic astrocytoma

1. Low cellularity without mitoses or anaplasia
2. Classically biphasic
  • Fibrillar
  • Microcystic
3. Hair-like fibres best observed on smear or with GFAP
4. Rosenthal fibres
5. Eosinophilic granular bodies
6. Microvascular proliferation
7. Focal pseudopalisading necrosis

Low-grade astrocytoma

1. Stellate, spindle-shaped tumor cells with fiber like processes
2. Large eosinophilic cytoplasmic mass
3. Forms microcysts

Anaplastic astrocytoma

1. Astrocytic tumor cells with:

Glioblastoma multiforme

1. Astrocytic tumor cells with:

Oligodendroglioma

1. Diffusely growing tumor
2. Highly cellular lesion resembling fried eggs with:

Ependymoma

1. Tadpole-shaped cells resembling an ice cream cone
2. Nuclear features monotonous, i.e. "boring"
  • Little variation in size, shape, and staining
3. Rosettes: circular nuclear free zones/cells arranged in a pseudoglandular fashion (2 types)
  • Perivascular pseudorosettes: tumor cells arranged around a blood vessel; nuclei of cells distant from the blood vessel, i.e. rim of cytoplasm (from tumor cells) surrounding blood vessel (nucleus-free zone). More common than ependymal rosette but less specific
  • Ependymal rosette (true ependymal rosette): rosette has an empty space at the centre


Images shown below are courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology

CNS: Pilocytic astrocytoma: variations in histologic appearance. As illustrated, many lesions are composed largely of spongy tissue rich in microcysts. Characteristic of pilocytic astrocytomas in general, the lesion is largely a solid mass of neoplastic cells without an obvious background of infiltrated brain. CNS: Pilocytic astrocytoma: variations in histologic appearance. The perivascular radiating processes in some lesions can create a likeness to an ependymoma. Note the spongy background unusual for ependymomas. CNS: Pilocytic astrocytoma: variations in histologic appearance. Other pilocytic astrocytomas are solid, rather than microcystic, and may be lobular. CNS: Pilocytic astrocytoma: variations in histologic appearance. Rosenthal fibers, usually confined to the solid rather than spongy regions are found in many pilocytic astrocytomas, but are not requisite for the diagnosis. CNS: Pilocytic astrocytoma: variations in histologic appearance. Rosenthal fibers are extremely abundant in some lesions. Particularly in the cerebellum, it can be difficult to distinguish such solid, paucicellular, highly fibrillar pilocytic astrocytomas from reactive gliosis with abundant Rosenthal fiber formation. CNS: Pilocytic astrocytoma: variations in histologic appearance. A loose array of polar cells creates an additional variant of pilocytic astrocytoma. CNS: Pilocytic astrocytoma: variations in histologic appearance. Some pilocytic astrocytomas are traversed by prominent collagenous septa. CNS: Pilocytic astrocytoma: variations in histologic appearance. Unusual pilocytic astrocytomas have an extensive mucinous background without microcysts. CNS: Comparison of normal optic nerve and pilocytic astrocytoma of the optic nerve. These two figures compare, at the same magnification, the normal optic nerve (left) with one containing a pilocytic astrocytoma (right). The neoplasm enlarges the compartments of the nerve and extends in collar-like fashion into the subarachnoid space. CNS: Pilocytic astrocytoma; The "hair cells" for which this lesion is named are readily seen. CNS: Pilocytic astrocytoma; Nuclear hyperchromasia and pleomorphism are common. Note the typical cellular elongation, and, at the center of the illustration, the eosinophilic granular body that populates pilocytic astrocytomas and certain other slowly growing gliomas. CNS: Pilocytic astrocytoma; Intracytoplasmic Rosenthal fibers are prominent in some pilocytic neoplasms. Brain: Malignant ependymoma: Micro med mag H&E tumor cells. CNS: Oligodendroglioma; Occasional oligodendrogliomas contain cells with minute, refractile eosinophilic bodies representing miniature Rosenthal fibers. CNS: Oligodendroglioma; The cells of some oligodendrogliomas acquire sufficient cytoplasm and process formation to become decidedly astrocytic, but their nuclei retain the roundness, uniformity, and chromatin distribution typical of oligodendroglioma. Anaplastic oligodendroglioma: Anaplastic oligodendrogliomas are highly cellular and associated with vascular proliferation. CNS: Oligodendroglioma (frozen section); Oligodendrogliomas in frozen sections lack the distinctive halos so often seen in permanent sections. Cellular monomorphism and infiltration of cerebral cortex with perineuronal satellitosis suggest the correct diagnosis. CNS: Clear cell ependymoma; Perinuclear clearing similar to that seen in oligodendrogliomas is a prominent feature of the clear cell variant. Note the vague perivascular pseudorosettes. The lesion was a discrete occipital intraventricular mass. CNS: Glioblastoma multiforme; Brain: Glioblastoma multiforme. Grade I-Ii: Micro med mag with H&E, tumor well shown CNS: Glioblastoma multiforme arising in an astrocytoma. At higher magnification, gemistocytic astrocytoma with microcystic change is apparent at the bottom of the illustration and cellular nodules of glioblastoma multiforme are seen at the top. The 6-year history of symptoms attested to the initially low-grade nature of this astrocytic tumor. CNS: Glioblastoma multiforme; Characteristic of most glioblastomas are small cells with elongated nuclei and bipolar processes. As here, the chromatin is generally not markedly dense nor are nucleoli usually prominent. CNS: Glioblastoma multiforme; Vascular proliferation, a common feature of glioblastoma, produces tufts which often grow directionally. Here, as is often the case, they are oriented toward a focus of necrosis (top right). CNS: Glioblastoma multiforme; At high magnification, the neovascular tuft is a mass which, as can be confirmed by immunohistochemistry, is formed of both endothelial cells and smooth muscle cells (pericytes). CNS: Glioblastoma multiforme; In many instances, necrosis is surrounded by a distinctive collar of cells, which are often smaller than those in surrounding neoplastic tissue. The phenomenon is referred to as pseudopalisading. CNS: Cerebrospinal dissemination of glioblastoma multiforme; As seen at low (left) and high (right) magnification, the small undifferentiated-appearing cells of this glioblastoma are drop metastases colonizing the nerve roots of the cauda equina. CNS: Cerebrospinal dissemination of glioblastoma multiforme; As seen at low (left) and high (right) magnification, the small undifferentiated-appearing cells of this glioblastoma are drop metastases colonizing the nerve roots of the cauda equina. CNS: Glioblastoma multiforme; Higher magnification reveals the small cell nature of such tumors. CNS: Glioblastoma multiforme; Some glioblastomas are especially infiltrative of the cerebral cortex where subpial, perivascular, and perineuronal accumulations are prominent. CNS: Glioblastoma multiforme; Although this densely cellular and largely undifferentiated lesion technically merits a diagnosis of anaplastic astrocytoma, it is, for practical purposes, a glioblastoma. Brain: Glioblastoma multiforme malignant astrocytoma Brain: Glioblastoma multiforme; pallisading Brain: Glioblastoma multiforme; vascular proliferation Brain: Glioblastoma multiforme; Plump and juicy endothelial cells, extravasated blood Brain: Glioblastoma multiforme; perivascular lymphocytes Brain: Glioblastoma multiforme; thrombosed vessel Brain: Glioblastoma multiforme; Hemosiderin in glioblastoma

References

  1. ↑ 1.0 1.1 1.2 Pathology of glioma. http://www.surgwiki.com/wiki/Intracranial_tumours,_infection_and_aneurysms#MANAGEMENT
  2. ↑ 2.0 2.1 Pathology of glioma. Wikipedia. https://en.wikipedia.org/wiki/Glioma
  3. ↑ 3.0 3.1 3.2 Schwartzbaum JA, Fisher JL, Aldape KD, Wrensch M (2006). "Epidemiology and molecular pathology of glioma". Nat Clin Pract Neurol. 2 (9): 494–503, quiz 1 p following 516. doi:10.1038/ncpneuro0289. PMID 16932614.
  4. ↑ Dubois LG, Campanati L, Righy C, D'Andrea-Meira I, Spohr TC, Porto-Carreiro I; et al. (2014). "Gliomas and the vascular fragility of the blood brain barrier". Front Cell Neurosci. 8: 418. doi:10.3389/fncel.2014.00418. PMC 4264502. PMID 25565956.
  5. ↑ 5.0 5.1 Pathology of gliomas. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma


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