Journal List > J Korean Soc Radiol > v.78(2) > 1095509

Park, Lee, Park, Kim, Lim, Kang, Kim, and Cho: Rapidly Growing Anaplastic Ganglioglioma Mimicking Brain Metastasis in a Middle-Aged Woman: A Case Report

Abstract

Anaplastic gangliogliomas (AGGs), the malignant counterpart of gangliogliomas, are classified as grade III tumors by the World Health Organization. Although, the clinical course and optimal treatment of AGGs are not well understood, they often result in worse local control rate and shorter survival. The authors describe the magnetic resonance imaging findings of a middle-aged woman with supratentorial AGG, that manifested as a rapidly growing cystic mass which mimicked metastasis. The authors suggest that AGG may be considered as a possible diagnosis for a rapidly growing peripheral enhancing mass in the brain, especially when it is superficially located.

References

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Fig. 1.
Anaplastic ganglioglioma with rapid tumor growth in a 68-year-old woman. A. Axial T1 (left upper panel) and T2 (right upper panel) magnetic resonance images showing a cystic mass with a mild surrounding edema in the right superior frontal gyrus. The gradient echo image (left under panel) shows a dark signal intensity within the mass, suggesting calcification or hemorrhage. The contrast-enhanced T1WI (right under panel) shows a peripheral ring enhancement. B. Approximately 2 months after the initial magnetic resonance scan, follow-up precontrast- (left panel) and contrast-enhanced (right panel) brain computed tomography images showing a rapidly growing peripheral enhancing cystic mass with septation and peripheral calcification in the right superior frontal gyrus, with a maximum diameter of 1.6 cm. GRE = gradient echo sequence, T1WI = T1-weighted image, T2WI = T2-weighted image Anaplastic ganglioglioma with rapid tumor growth in a 68-year-old woman. C. Microscopic finding showing the histopathological features of anaplastic ganglioglioma in our case. Biphasic neoplasm with calcification. Neuronal (black arrowhead) and astrocytic components (white arrowhead; H&E, original magnification, × 40, left upper panel). The immunostaining features are suggestive of ganglioglioma. The neoplastic glial components are positive for Olig2 (anti-Olig2 immunohistochemistry, × 40, right upper panel), and the ganglion cells are positive for NeuN (anti-NeuN immunohistochemistry, × 40, left under panel). Anaplastic pathological features include focal necrosis and endothelial proliferation (H&E, original magnification, × 100, right under panel). H&E = hematoxylin-eosin stain Anaplastic ganglioglioma with rapid tumor growth in a 68-year-old woman. D. Postoperative evaluation was performed 3 months after the surgical resection. FLAIR (left upper panel) and contrast-enhanced (right upper panel) magnetic resonance images showing an irregular peripheral enhancing lesion with a maximum diameter of 1.9 cm and a surrounding edema along the resection margin. DSC perfusion image (left under panel) shows increased cerebral blood volume (white arrow), and ASL perfusion image (right under panel) shows increased cerebral blood flow (white arrow). These findings suggest tumor recurrence. ASL = arterial spin labelling, DSC = dynamic susceptibility contrast, FLAIR = fluid-attenuated inversion recovery, T1WI = T1-weighted image
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Table 1.
Reported Cases of Brain Anaplastic Ganglioglioma between 2007 and 2016 in the English Literature
Authors Year of Publication Sex/Age Clinical Manifestation Location of Lesion Management Follow-Up Periods Follow-Up Results
Kang et al. 2007 F/45 Headache Left frontal lobe Total resection, adjuvant chemo- and radiotherapy 35 months Recovery
Mittelbronn et al. 2007 F/47 None Left frontal lobe Surgical resection 60 months Recovery
Kawataki et al. 2010 M/34 Seizure Left temporal lobe Subtotal resection 6 months Death
DeMarchi et al. 2011 M/61 Headache Left temporal lobe Total resection 29 months Death
Reis et al. 2012 M/9 Seizure Right cingulate gyrus Biopsy 48 months Local recur
              and alive
Gonzalez et al. 2012 M/33 Right side weakness Pons and midbrain Biopsy 16 months Death
Scoccianti et al. 2012 M/14 Seizure Left frontoparietal lobe Tumor resection 72 months Recovery
Lucas et al. 2015 M/12 Headache Left temporoparietal lobe Surgical resection 23 months Death
    M/11 Seizure Left medial temporal lobe Radiotherapy and resection 16 months Death
        and hypothalamus      
    M/34 Headache Right medial temporal lobe Surgical resection 22 months Death
Costa et al. 2016 F/32 Headache Pineal gland Gross total resection 4 days Recovery
Martinez et al. 2016 M/21 Headache Left temporal lobe Surgical resection 24 months Death
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