A glomus tumour is a nodule that forms from glomus cells within the arterial component of the glomus body, or succulent-Hoyer canal. These tumours most often present on an adult’s palm or nail bed and are extremely tender, especially after a change in temperature or pressure.
Extracutaneous glomus tumours are rare but may occur in the gastrointestinal tract, mediastinum, trachea, mesentery, cervix, and vagina.
In the head and neck region, glomus tumours can occur in the following locations:
Glomus tumours often appear as a small, firm, reddish-blue swelling under the fingernail, usually less than 7 mm in diameter. They may be:
The precise cause of glomus tumours is not fully understood.
Some glomus tumours are linked to inherited genetic mutations that may be passed to children. Genetic screening is advised for families with a history of glomus tumours. However, these tumours can also occur sporadically due to gene mutations developed over time.
Diagnosis typically requires an ENT or tumour specialist. During examination, signs include:
X-rays may show deformity or erosion of the distal phalanx in long-standing cases. MRI is the investigation of choice for confirming the diagnosis.
The primary treatment for glomus tumours is surgical removal. The approach may vary depending on the tumour’s location and nature:
All treatment plans should be reviewed by an interdisciplinary tumour board including specialists in oncology, endocrinology, radiology, surgery, pathology, and psycho-oncology.
The exact development mechanism remains unclear, but glomus tumours are more common in women and may have a hereditary component. No specific criteria currently exist to predict their frequency or association with other conditions.
Prevention is not currently possible, as many causes are unknown. While smoking and other carcinogens may contribute, even hereditary forms of glomus tumours cannot be stopped in advance.
For individuals diagnosed with hereditary paraganglioma syndromes, routine screening is essential. This includes annual clinical evaluations, lab tests, and imaging from the skull base to pelvis every 2–3 years, typically via MRI.
Outcomes depend on whether the tumour is benign (about 60%) or malignant (about 40%). Malignant tumours require prompt surgery. However, even benign tumours can be locally destructive and potentially metastasize later.
Due to the complexity and potential severity, early diagnosis, timely treatment, and regular follow-up at a specialized centre are critical for the best prognosis.
Tender Palm Super-Speciality Hospital has the most trusted team of ENT specialists and surgeons with advanced diagnostic equipment care for Glomus Tumours treatment in Lucknow, India. Our ENT department follows international safety standards and has years of experience in treating Skull Base related Disease and Conditions.
Call us at +91-9076972161
Email at care@tenderpalm.com