Oligodendroglioma other diagnostic studies: Difference between revisions

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'''Indications for different types of biopsies'''
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[[craniotomy|Open biopsy]]
[[craniotomy|Open biopsy]]
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*Surgically resectable masses
*[[Surgery|Surgically]] [[Resection|resectable]] [[Mass|masses]]
*Lesions in accessible and relatively “silent” areas of the brain or in areas of the brain with a mild postoperative neurologic deficit
*[[Lesions]] in [[Accessible image|accessible]] and [[Relatively compact|relatively]] “[[Silent News|silent]]” [[Area|areas]] of the [[brain]] or in [[Area|areas]] of the [[brain]] with a mild postoperative [[Neurological|neurologic]] deficit
*Appearance consistent with [[tumor]] on the [[MRI]]
*[[Appearance]] consistent with [[tumor]] on the [[MRI]]
*Large [[tumors]] exerting mass effect
*Large [[tumors]] exerting [[mass effect]]
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[[Stereotactic|Stereotactic biopsy]]
[[Stereotactic|Stereotactic biopsy]]
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*Deep-seated [[tumor]] that is not amenable to resection
*Deep-seated [[tumor]] that is not amenable to [[resection]]
*Lesions in which the radiological and clinical findings are ambiguous
*[[Lesions]] in which the [[radiological]] and [[clinical]] findings are ambiguous
*Diffuse or multiple lesions
*[[Diffuse]] or multiple [[lesions]]
*Appearance that suggests a [[lymphoma]], which would not require resection
*[[Appearance]] that [[Suggestion|suggests]] a [[lymphoma]], which would not require [[resection]]
*Change in the appearance of a previously diagnosed or treated [[tumor]]
*[[Change detection|Change]] in the [[appearance]] of a previously [[Diagnose|diagnosed]] or [[Treatments|treated]] [[tumor]]
*Assessment of tumor after treatment (to distinguish between [[radiation|radiation necrosis]] and tumor recurrence)
*[[Assessment and Plan|Assessment]] of [[tumor]] after [[Treatments|treatment]] (to distinguish between [[radiation|radiation necrosis]] and [[tumor]] [[Recurrence plot|recurrence]])
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Revision as of 23:36, 18 May 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sara Mohsin, M.D.[2]Sujit Routray, M.D. [3]

Overview

Other diagnostic studies for oligodendroglioma include biopsy (homogeneous, compact, rounded cells with distinct borders and clear cytoplasm surrounding a dense central nucleus and perinuclear halo) and fluorescent in-situ hybridization (FISH) technique (deletions of chromosome 1p and 19q).

Other Diagnostic Studies

Biopsy

Indications for different types of biopsies
Type of biopsy Indications

Open biopsy

Stereotactic biopsy

Fluorescent in-situ hybridization (FISH) technique

References

  1. Wesseling P, van den Bent M, Perry A (2015). "Oligodendroglioma: pathology, molecular mechanisms and markers". Acta Neuropathol. 129 (6): 809–27. doi:10.1007/s00401-015-1424-1. PMC 4436696. PMID 25943885.
  2. Eskandar EN, Loeffler JS, O'Neill AM, Hunter GJ, Louis DN (2004). "Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 33-2004. A 34-year-old man with a seizure and a frontal-lobe brain lesion". N Engl J Med. 351 (18): 1875–82. doi:10.1056/NEJMcpc049025. PMID 15509821.
  3. Ersen, Ayca (2008), Pathology of malignant gliomas: Challenges of everyday practice and the WHO 2007, Turkish Journal of Pathology, retrieved 9 October, 2015 Check date values in: |accessdate= (help)


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