Gangliocytomas are rare central nervous tumors mainly involving supratentorial region and occuring primarily in children and young adults. We present a rare case of gangliocytoma of medulla oblongata in a 48-year-old man demonstrating higher tracer uptake on positron emission tomography (PET) scans.A 48-year-old apparently healthy man was found to have an isodense suboccipital mass lesion with calcifications on CT brain check-up. T2-weighted MRI showed a mixed-intensity tumor with a small cyst in the right cerebellomedullary cistern (Fig. 1a). It was slightly enhanced on T1-weighted gadolinium-enhanced MRI scans. The tumor appeared to have arisen in the lateral part of the medulla oblongata with no clear demarcation from the brainstem. FDG- (Fig. 1b) and methionine PET ( Fig. 1c) studies were performed and measurement of the equilibrated radioactivity 5 min after the i.v. injection of FDG (211 MBq) and MET (200 MBq), respectively, clearly showed increased tracer uptake. On approaching the tumor via suboccipital craniotomy, a soft grayish mass in the cerebellomedullary cistern was seen involving the lower cranial nerves, which made us limit the intervention to biopsy (Fig. 1d). His postoperative course was uneventful.MRI studies performed 16 months later yielded no evidence of tumor growth. Hematoxylin and eosin staining showed scattered large to medium-sized atypical ganglion cells with ample cytoplasm containing Nissl bodies in a normocellular and non-neoplastic glial background (Fig. 1e). Immunohistochemically, the tumor cells were strongly positive for synaptophysin and neurofilament. The glial background was faintly positive for GFAP (photo not shown). The MIB-1 labeling index was \1%. CD31 immunohistochemistry revealed a moderately dense scattering of microvessels which were well branched and often enlarged (Fig. 1f).Gangliocytomas are composed of mature atypical neuronal cells that constitute the sole neoplastic components. The most common site of gangliocytoma is the cerebral hemisphere, the preferred site being the temporal lobe. In our patient the tumor arose in the lateral part of the medulla oblongata. It was primarily composed of multipolar cells with ample eosinophilic cytoplasm that included Nissl bodies distributed perisomatically. The cells were positive for synaptophysin and neurofilament. A few astrocytes without neoplastic features were also seen. To the best of our knowledge, ours is the 3rd documented case of gangliocytoma arising in the brainstem. The two patients reported earlier were a 12 year-old boy [1] and an infant with prolonged expiratory apnea with progressively increasing severity [2].Our PET studies showed interesting findings. Although the lesion was a benign tumor with low cellularity, it manifested increased uptake of tracers on FDG-and methionine PET scans. The mechanism of high FDG uptake in malignant tumors is attributable to several factors including an increased overall cell metabolism, the upregulation of enzymatic activity of Glut-1 or hexokinase, and increased cell dens...