Outcome and Prognosis
Glomus jugulare tumors may grow slowly and produce cranial nerve palsies that, to a certain point, are benign and mostly cosmetic. However, despite this optimistic assessment, a recent study showed a long-term reduced quality of life in patients with glomus tumors.1
The mortality rate is 6.2% among patients treated with radiation and 2.5% among those treated surgically. The overall mortality rate is 8.7%.
Twenty years after treatment, the survival rate is 94%, and 77% of patients remain symptom free. In 1945, Rosenwasser described the first patient diagnosed with glomus jugulare tumor. The patient survived until 1987.5
Future and Controversies
Surgery is the treatment of choice for glomus tumors, and its effectiveness will improve with intraoperative guiding and imaging systems.
The cooperative work of neurosurgeons and neuro-otologists to surgically resect Fisch type A, B, and C tumors has proven to be of value. However, definitive optimal treatment of type D glomus jugulare tumor is still controversial.
Because of its long-term effects on the bone and brain, radiation that is not stereotactically targeted is outdated. Radiosurgery with its influence on neuro-oncology must be proven useful in treatment of these slowly growing tumors.14
Continued tumor growth and postsurgical damage to the lower cranial nerves are issues that still need to be successfully addressed.
Recent genetic research on familial glomus jugulare tumors suggests future directions of treatment towards gene manipulation.
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References
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Further Reading
Keywords
glomus tumors, glomus jugulare tumor, paraganglioma, chemodectoma, nonchromaffin paraganglia, temporal bone tumor, ganglia tympanica, glandula tympanica, vascular tumors of the middle ear, conductive hearing loss, pulsatile tinnitus, ear fullness, otorrhea, hemorrhage, bruit, middle ear mass, ringing in the ears, deafness
Follow-up: Glomus Tumors