Glomus tumors are rare benign myoepithelial neoplasms that can present with intractable pain. We report the case of a 59-year-old gentleman who presented with upper abdominal and chest pain caused by a posterior mediastinal glomus tumor arising from the spinal column, which required surgical resection. As glomus tumors usually develop in the limbs, this case highlights the complexity of diagnosis and treatment of glomus tumors when they present in rare locations.
SchieferTKParkerWLAnakwenzeOAAmadioPCInwardsCYSpinnerRJ. Extradigital glomus tumors: a 20-year experience. Mayo Clin Proc2006; 81: 1337–1344.
2.
MiliaMETurriLBeldiDDeantonioLPareschiRKrengliM. Multidisciplinary approach in the treatment of malignant paraganglioma of the glomus vagale: a case report. Tumori2011; 97: 225–228.
BoonLMBrouillardPIrrthumA. A gene for inherited cutaneous venous anomalies (“glomangiomas”) localizes to chromosome 1p 21-22. Am J Hum Genet1999; 65: 125–133.
5.
ParkHJJeonYHKimSS. Gray-scale and color Doppler sonographic appearances of nonsubungual soft-tissue glomus tumors. J Clin Ultrasound2011; 39: 305–309.
6.
NoujaimSEPattekarMACacciarelliASandersWPWangAM. Paraganglioma of the temporal bone: role of magnetic resonance imaging versus computed tomography. Top Magn Resonan Imaging2000; 11: 108–122.
7.
ChristieATeasdaleE. A comparative review of multidetector CT angiography and MRI in the diagnosis of jugular foramen lesions. Clin Radiol2010; 65: 213–217.