Journal of Pediatric Neurology 2021; 19(05): 355-358
DOI: 10.1055/s-0040-1721402
Case Report

Pediatric Malignant Glomus Tumor of the Cervical Paraspinal Tissue: Case Report and Review of the Literature

Andrea Ziegler
1   Department of Otolaryngology, Loyola University Medical Center, Maywood, Illinois, Unites States
,
Eric Thorpe
1   Department of Otolaryngology, Loyola University Medical Center, Maywood, Illinois, Unites States
› Author Affiliations
Funding None.

Abstract

Glomus tumors are mesenchymal tumors that arise from glomus bodies and most frequently occur in the distal extremities. These tumors can occur throughout the body and are typically benign. However, a very small fraction of glomus tumors displays aggressive features and are considered atypical or malignant. We report on our experience and management of the first case in the literature of a malignant glomus tumor in a child originating in the paraspinal region with involvement of the cervical spine. Malignant glomus tumors tend to be locally aggressive, and en bloc resection is difficult, especially when the tumors occur in the head and neck. Additional studies on disease progression and adjuvant treatment outcomes are necessary to determine the best treatment approach and long-term outcomes in patients with malignant glomus tumors.

Note

This research has not been presented elsewhere.




Publication History

Received: 14 September 2020

Accepted: 26 October 2020

Article published online:
02 December 2020

© 2020. Thieme. All rights reserved.

Georg Thieme Verlag KG
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  • References

  • 1 Brathwaite CD, Poppiti Jr RJJ. Malignant glomus tumor. A case report of widespread metastases in a patient with multiple glomus body hamartomas. Am J Surg Pathol 1996; 20 (02) 233-238
  • 2 Boros AL, Davis JP, Sedghizadeh PP, Yamashita DDR. Glomus tumor: report of a rare case affecting the oral cavity and review of the literature. J Oral Maxillofac Surg 2010; 68 (09) 2329-2334
  • 3 Aslam N, Qazi ZUS, Ahmad AH, Khan RU. Malignant glomus tumour of larynx: first case report and literature review. J Laryngol Otol 2012; 126 (07) 743-746
  • 4 Chou T, Pan SC, Shieh SJ, Lee JW, Chiu HY, Ho CL. Glomus tumor: twenty-year experience and literature review. Ann Plast Surg 2016; 76 (Suppl. 01) S35-S40
  • 5 Wolter NE, Adil E, Irace AL. et al. Malignant glomus tumors of the head and neck in children and adults: Evaluation and management. Laryngoscope 2017; 127 (12) 2873-2882
  • 6 Mravic M, LaChaud G, Nguyen A, Scott MA, Dry SM, James AW. Clinical and histopathological diagnosis of glomus tumor: an institutional experience of 138 cases. Int J Surg Pathol 2015; 23 (03) 181-188
  • 7 Grampurohit VU, Myageri A, Annigeri V, Rao R. Glomangiosarcoma de novo in a child: a case report and review of literature. Saugi Surg J. 2014; 2: 60-62
  • 8 Folpe AL, Fanburg-Smith JC, Miettinen M, Weiss SW. Atypical and malignant glomus tumors: analysis of 52 cases, with a proposal for the reclassification of glomus tumors. Am J Surg Pathol 2001; 25 (01) 1-12
  • 9 Jin WS, Jeon IS. A case of malignant glomus tumor on shoulder with pulmonary metastasis treated with doxorubicin and ifosfamide in a 10 year old girl. Clin Pediatr Hematol Oncol 2016; 23: 65-69
  • 10 Matsumoto K, Kakizaki H, Yagihashi N, Yagihashi S. Malignant glomus tumor in the branchial muscle of a 16-year-old girl. Pathol Int 2001; 51 (09) 729-734
  • 11 Swift CC, Eklund MJ, Kraveka JM, Alazraki AL. Updates in diagnosis, management, and treatment of neuroblastoma. Radiographics 2018; 38 (02) 566-580
  • 12 Chung DH, Kim NR, Kim T. et al. Malignant glomus tumor of the thyroid gland where is heretofore an unreported organ: a case report and literature review. Endocr Pathol 2015; 26 (01) 37-44