Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2014 Dec 19:11:63-8.
eCollection 2015 Jan-Apr.

Glomus tumor of the thenar eminence in neurofibromatosis type 1: case report and literature review

Affiliations

Glomus tumor of the thenar eminence in neurofibromatosis type 1: case report and literature review

Gabriele Scaravilli et al. Transl Med UniSa. .

Abstract

Neurofibromatosis type 1 (NF1) is a disease characterized by increased tumorigenesis susceptibility, caused by mutations of the oncosuppressor gene NF1. The glomus tumor (GT) is a rare, very painful mesenchymal neoplasm, arising from the glomus body. In recent years, it has been highlighted the association between NF1 and GT. We report a case of a man aged 65 years, suffering from NF1, with intense pain at the thenar eminence of the right hand, successfully treated with the excision of the mass.

Keywords: Biallelic Inactivation; Finger; Glomic Tumor; Neurofibromatosis; Pain.

PubMed Disclaimer

Figures

Figure 1:
Figure 1:
Eminence thenar of the right hand with the areas where the neoformation was found (black arrows) and the Love test was positive.
Figure 2:
Figure 2:
Typical neurofibromas along the trunk and back of the patient
Figure 3:
Figure 3:
Thermography show the hyperthermic area in the thenar eminence of the right hand where the glomus tumor was located (red arrow).
Figure 4:
Figure 4:
Intraoperative findings. The glomus tumor was excised through a volar approach and was found to to be very shallow. The window on the left top shows the well capsulated neoformation as it appeared at the end of the procedure.
Figure 5:
Figure 5:
Histological findings: blood vessels surrounded by a proliferation of small round cells with dark nuclei in a myxoid stroma.

References

    1. Scalzone M, Coccia P, Ruggiero A, Riccardi R. Neurofibromatosis type 1 clinical features and management. Pediatr Med Chir. 2009 Nov-Dec;31(6):246–51. - PubMed
    1. Harrisingh MC, Lloyd AC. Ras/Raf/ERK signalling and NF1. Cell Cycle. 2004 Oct;3(10):1255. - PubMed
    1. Huson S. Neurofibromatosis: emerging phenotypes, mechanisms and management. Clin Med. 2008 Dec;8(6):611–7. - PMC - PubMed
    1. Ferner RE, Huson SM, Thomas N, Moss C, Willshaw H, Evans DG, Upadhyaya M, Towers R, Gleeson M, Steiger C, Kirby A. Guidelines for the diagnosis and management of individuals with neurofibromatosis 1. J Med Genet. 2007 Feb;44(2):81–8. Epub 2006 Nov 14. Review. - PMC - PubMed
    1. Gombos Z, Zhang PJ. Glomus tumor. Arch Pathol Lab Med. 2008 Sep;132(9):1448–52. - PubMed

LinkOut - more resources