eMedicine Specialties > Neurology > Neuro-oncology

Oligodendroglioma: Differential Diagnoses & Workup

Author: ABM Salah Uddin, MD, Consulting Staff, Department of Internal Medicine, St Vincent's Hospital
Coauthor(s): Tambi Jarmi, MD, Resident Physician, Department of Internal Medicine, Carraway Methodist Medical Center
Contributor Information and Disclosures

Updated: May 4, 2009

Differential Diagnoses

Arteriovenous Malformations
Low-Grade Astrocytoma
Brainstem Gliomas
Meningioma
CNS Melanoma
Metastatic Disease to the Brain
Frontal Lobe Syndromes
Primary CNS Lymphoma
Glioblastoma Multiforme
HIV-1 Associated Opportunistic Infections: CNS Toxoplasmosis
HIV-1 Associated Opportunistic Neoplasms: CNS Lymphoma

Other Problems to Be Considered

Other CNS tumors (eg, meningioma, metastasis, astrocytoma, glioblastoma)
Brain abscess
CNS toxoplasmosis
Lymphoma
Vascular malformations

Workup

Laboratory Studies

Routine laboratory workup is not helpful. If seizures are noted, include EEG, serum electrolyte studies, and if necessary a lumbar puncture in the metabolic workup for seizure, after excluding intracranial pathology with an imaging study. These routine tests help exclude other causes of seizure (eg, electrolyte imbalance, metabolic abnormalities).

Imaging Studies

Diagnostic imaging studies are the most important part of the workup.

  • MRI (with and without gadolinium) is the preferred modality.
    • T1 images generally demonstrate a hypointense or mixed hypointense and hyperintense mass.
    • T2 images reveal a hyperintense mass with or without surrounding edema.
    • With contrast administration, the LGO generally does not enhance, while an anaplastic oligodendroglioma does enhance. These tumors also tend toward calcification.

      Sagittal gadolinium-enhanced T1-weighted magnetic...

      Sagittal gadolinium-enhanced T1-weighted magnetic resonance image of a low-grade oligodendroglioma. This image demonstrates no contrast enhancement.

      Sagittal gadolinium-enhanced T1-weighted magnetic...

      Sagittal gadolinium-enhanced T1-weighted magnetic resonance image of a low-grade oligodendroglioma. This image demonstrates no contrast enhancement.

  • A study by Megyesi et al compared the MRI characteristics of oligodendroglioma with 1p/19q loss with those without 1p/19q loss. Tumors with 1p/19q loss were significantly more likely to have indistinct borders, a mixed signal intensity on T1- and T2-weighted images, paramagnetic susceptibility effects, and intratumoral calcification compared with oligodendroglioma without 1p/19q loss, which more often had a distinct border and a uniform signal on T1- and T2-weighted images.2
  • A study by Brown et al, using noninvasive quantitative MRI with and without contrast, reliably predicted the co-deletion of chromosomes 1p and 19q with high sensitivity and specificity in suspected low-grade glioma.3
  • CT scans reveal a hypodense, reasonably well-demarcated mass with moderate surrounding edema.
    • Intratumoral calcification is common, and hemorrhage is noted occasionally.
    • As with contrast MRI, the tumor does not enhance unless it is behaving unusually aggressively or has an anaplastic astrocytic component.

      Contrast-enhanced computed tomography scan in a 4...

      Contrast-enhanced computed tomography scan in a 44-year-old man with a 3-year history of epileptic seizures. This image reveals a calcified hypoattenuating lesion that is invading the corpus callosum.

      Contrast-enhanced computed tomography scan in a 4...

      Contrast-enhanced computed tomography scan in a 44-year-old man with a 3-year history of epileptic seizures. This image reveals a calcified hypoattenuating lesion that is invading the corpus callosum.



      Computed tomography scan of a low-grade oligodend...

      Computed tomography scan of a low-grade oligodendroglioma. This image reveals a well-demarcated, left frontal hypoattenuating lesion with a small calcification.

      Computed tomography scan of a low-grade oligodend...

      Computed tomography scan of a low-grade oligodendroglioma. This image reveals a well-demarcated, left frontal hypoattenuating lesion with a small calcification.

Other Tests

Definite diagnosis in confirmed by stereotactic or open biopsy of the lesion. Currently, MR spectroscopy is performed regularly in some centers to differentiate the tumor from other benign lesions and to define the aggressiveness of the tumor, although this is in the investigational phase. In the future, it may offer another noninvasive modality of investigation.

Histologic Findings

Macroscopic

Grossly, oligodendrogliomas appear as well defined, solid, and pinkish grey, frequently with areas of calcification and sometimes with areas of necrosis and cystic degeneration. Intratumoral hemorrhage may be present and in some patients may be massive and responsible for sudden death.

Microscopic

Oligodendrogliomas are distinctive, consisting of homogeneous, compact, rounded cells with distinct borders and clear cytoplasm surrounding a dense central nucleus, giving them a "fried egg" appearance.

Classic histologic image of oligodendroglioma. Th...

Classic histologic image of oligodendroglioma. This image shows monomorphous tumoral proliferation that consists of round, regular cells with a small, central, hyperchromatic nucleus surrounded by clear cytoplasm. Few calcifications are present.

Classic histologic image of oligodendroglioma. Th...

Classic histologic image of oligodendroglioma. This image shows monomorphous tumoral proliferation that consists of round, regular cells with a small, central, hyperchromatic nucleus surrounded by clear cytoplasm. Few calcifications are present.


Oligodendrogliomas usually arise in the subcortical location but infiltrate diffusely into cortex around normal neuronal elements and, in superficially located lesions, may extend to the leptomeninges. Within the tumor, branching blood vessels are highly characteristic and divide the cells into discrete clusters. Many oligodendrogliomas have some component of astrocytoma within them; however, distinguishing neoplastic astrocytes from reactive astrocytes may be very difficult. Clearly, some tumors are truly mixed oligoastrocytic tumors; both cell types are believed to arise from a common oligodendrocyte precursor termed the oligodendrocyte type-2 astrocyte.

To call a tumor a mixed oligoastrocytoma, the minimum proportion of astrocyte is variable but ranges from 10-25%. In most instances, the diagnosis of oligodendroglioma is apparent. Confusion can arise with intraventricular oligodendrogliomas, which can appear similar to central neurocytoma. Under light microscopy, neuronal differentiation (eg, Homer Wright rosette formation) can indicate a diagnosis of central neurocytoma, but immunohistochemical markers such as synaptophysin may be necessary to confirm the diagnosis.4

Most oligodendrogliomas are slow-growing indolent tumors; however, they occasionally behave in a more malignant manner when initially diagnosed, or an indolent tumor may evolve into an aggressive one. Malignant tumors demonstrate increased cellularity, nuclear pleomorphism, endothelial proliferation, mitotic activity, and necrosis. Different grading systems are available for malignant tumors, but most pathologists use a simple two-tier grading system, diagnosing tumors without anaplastic features as oligodendroglioma tumors and as anaplastic oligodendroglioma if several of the malignant features are present.5

Smear preparation of anaplastic oligodendroglioma...

Smear preparation of anaplastic oligodendroglioma. This image reveals increased nuclear pleomorphism and vascular proliferation.

Smear preparation of anaplastic oligodendroglioma...

Smear preparation of anaplastic oligodendroglioma. This image reveals increased nuclear pleomorphism and vascular proliferation.

Staging

No other staging workup is required.

More on Oligodendroglioma

Overview: Oligodendroglioma
Differential Diagnoses & Workup: Oligodendroglioma
Treatment & Medication: Oligodendroglioma
Follow-up: Oligodendroglioma
Multimedia: Oligodendroglioma
References

References

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  2. Megyesi JF, Kachur E, Lee DH, et al. Imaging correlates of molecular signatures in oligodendrogliomas. Clin Cancer Res. Jul 1 2004;10(13):4303-6. [Medline].

  3. Brown R, Zlatescu M, Sijben A, Roldan G, Easaw J, Forsyth P. The use of magnetic resonance imaging to noninvasively detect genetic signatures in oligodendroglioma. Clin Cancer Res. Apr 15 2008;14(8):2357-62. [Medline].

  4. Yuen ST, Fung CF, Ng TH, Leung SY. Central neurocytoma: its differentiation from intraventricular oligodendroglioma. Childs Nerv Syst. Oct 1992;8(7):383-8. [Medline].

  5. Burger PC, Rawlings CE, Cox EB, et al. Clinicopathologic correlations in the oligodendroglioma. Cancer. Apr 1 1987;59(7):1345-52. [Medline].

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  8. Cairncross G, Macdonald D, Ludwin S, et al. Chemotherapy for anaplastic oligodendroglioma. National Cancer Institute of Canada Clinical Trials Group. J Clin Oncol. Oct 1994;12(10):2013-21. [Medline].

  9. van den Bent MJ, Taphoorn MJ, Brandes AA, et al. Phase II study of first-line chemotherapy with temozolomide in recurrent oligodendroglial tumors: the European Organization for Research and Treatment of Cancer Brain Tumor Group Study 26971. J Clin Oncol. Jul 1 2003;21(13):2525-8. [Medline][Full Text].

  10. Mohile NA, Forsyth P, Stewart D, Raizer JJ, Paleologos N, Kewalramani T, et al. A phase II study of intensified chemotherapy alone as initial treatment for newly diagnosed anaplastic oligodendroglioma: an interim analysis. J Neurooncol. Sep 2008;89(2):187-93. [Medline].

  11. Cairncross JG, Berkey B, Shaw E. Phase III trial of chemotherapy plus radiotherapy compared with radiotherapy alone for pure and mixed anaplastic oligodendrogliomas: intergroup Radiation Therapy Oncology Group Trial 9402. J Clin Oncol. 2006;24:2702-2714.

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  13. Bello MJ, Vaquero J, de Campos JM, et al. Molecular analysis of chromosome 1 abnormalities in human gliomas reveals frequent loss of 1p in oligodendroglial tumors. Int J Cancer. Apr 15 1994;57(2):172-5. [Medline].

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Further Reading

Keywords

oligodendroglioma, OD, LGO, anaplastic oligodendroglioma, glial brain tumor, intracranial tumors, low-grade oligodendrogliomas

Contributor Information and Disclosures

Author

ABM Salah Uddin, MD, Consulting Staff, Department of Internal Medicine, St Vincent's Hospital
ABM Salah Uddin, MD is a member of the following medical societies: American Academy of Neurology, American Epilepsy Society, and American Medical Association
Disclosure: Nothing to disclose.

Coauthor(s)

Tambi Jarmi, MD, Resident Physician, Department of Internal Medicine, Carraway Methodist Medical Center
Tambi Jarmi, MD is a member of the following medical societies: American College of Physicians and American Medical Association
Disclosure: Nothing to disclose.

Medical Editor

Amy A Pruitt, MD, Associate Professor of Neurology, University of Pennsylvania; Attending Neurologist, Hospital of the University of Pennsylvania
Amy A Pruitt, MD is a member of the following medical societies: American Academy of Neurology
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Jorge Kattah, MD, Head, Program Director, Professor, Department of Neurology, University of Illinois College of Medicine at Peoria
Jorge Kattah, MD is a member of the following medical societies: American Academy of Neurology, American Neurological Association, and New York Academy of Sciences
Disclosure: Biogen Honoraria Consulting; Bayer Corporation Honoraria Consulting

CME Editor

Selim R Benbadis, MD, Professor, Director of Comprehensive Epilepsy Program, Departments of Neurology and Neurosurgery, University of South Florida School of Medicine, Tampa General Hospital
Selim R Benbadis, MD is a member of the following medical societies: American Academy of Neurology, American Academy of Sleep Medicine, American Clinical Neurophysiology Society, American Epilepsy Society, and American Medical Association
Disclosure: Nothing to disclose.

Chief Editor

Stephen A Berman, MD, PhD, Professor, Department of Internal Medicine, Section of Neurology, Dartmouth Medical School; Chief, Neurology Service, White River Junction Veterans Medical Center
Stephen A Berman, MD, PhD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Neurology, and Phi Beta Kappa
Disclosure: Nothing to disclose.

 
 
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