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Relevant bibliographies by topics / Glomus tumors

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Academic literature on the topic 'Glomus tumors'

Author: Grafiati

Published: 7 June 2025

Last updated: 9 July 2025

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Journal articles on the topic "Glomus tumors"

1

Freire, Maxime, Brian Rubin, Steven Lietman, and Murali Sundaram. "Solitary glomus tumor recurring as multiple glomus tumors." Skeletal Radiology 41, no. 10 (2012): 1333–37. http://dx.doi.org/10.1007/s00256-012-1410-9.

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Hayashi, Mikihiko, Yasuyuki Kitagawa, Yong Kim, et al. "Malignant glomus tumor arising among multiple glomus tumors." Journal of Orthopaedic Science 13, no. 5 (2008): 472–75. http://dx.doi.org/10.1007/s00776-008-1250-6.

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Keles, Bahar, and Fred H. Linthicum. "Glomus Tumors." Otology & Neurotology 30, no. 4 (2009): 577–78. http://dx.doi.org/10.1097/mao.0b013e3181967bb4.

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McDermott, Erin M., and Arnold-Peter C. Weiss. "Glomus Tumors." Journal of Hand Surgery 31, no. 8 (2006): 1397–400. http://dx.doi.org/10.1016/j.jhsa.2006.05.018.

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Shanmugasamy, K., Sneha Mahendran, and S. Sowmya. "Extradigital glomus tumour of the forearm- A rare site for an unusual tumour." IP Journal of Diagnostic Pathology and Oncology 7, no. 1 (2022): 48–50. http://dx.doi.org/10.18231/j.jdpo.2022.010.

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Soft tissue tumors are known to occur by varied presentations with atypical features, especially with regard to vascular tumors. The glomus tumour is an unusual benign neoplasm arising from smooth muscles of the perivascular glomus bodies. While it is known to occur in the extremities, this tumour has a predilection for the sub-ungal region of fingers. Vascular tumors as such, especially glomus tumors presenting in extra digital sites are extremely rare. In literature only five cases are available on extra digital sites and few cases have been reported to involve the gastrointestinal tract, airways, shoulders, wrist, knees and elbows. This report discusses the clinical and histopathological features of an glomus tumour of the forearm with atypical presentation. Glomus tumours should be considered as a differential in any nodule occurring in the extradigital locations. Extradigital tumours need not present as a painful purplish nodule and can be asymptomatic. Surgeons and pathologists have to be aware about the varied presentation of these tumours so that misdiagnosis can be avoided and patient can undergo quicker diagnosis and treatment.

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Naji Rad, Sara, Samira Najirad, and Rana Rafiei. "A Rare Case of Glomus Tumor on the Mucosal Surface of Lower Lip." Journal of Investigative Medicine High Impact Case Reports 8 (January 2020): 232470962093615. http://dx.doi.org/10.1177/2324709620936159.

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Glomus tumors are mesenchymal neoplasms derived from glomus bodies with rare presentations in the oral cavity. Glomus tumors present as a purple or pink vascular nodule or papule, sized <1 cm, and imitate vascular neoplasms such as hemangiopericytoma or hemangioma. Glomus tumors represent less than 2% of all benign soft tissue tumors. Only 27 cases of benign glomus tumors with oral cavity involvement have been reported to date. The most-reported oral tumors involved the lips (54.2%), followed by hard palate, gingiva, tongue, and buccal mucosa. The mean age of presentation of the labial glomus tumors is 48.7 years, with no gender predilection, in contrast to the subungual site, which occurs more in females. The etiology of the glomus tumors remains unknown. Subungual glomus tumors present as stabbing pain, cold intolerance, and tenderness of the fingertips, whereas labial glomus tumors mostly present as a painless, small, and slow-growing lesion. Treatment is surgical resection of the tumor. The recurrence rate of labial glomus tumors is unclear. In this article, we present the case of a 62-year-old man with a 2-month history of painless, soft lump on the mucosal surface of the lower left lip. Excisional resection of the tumor was performed in the clinic, and the histopathologic finding was consistent with solid glomus tumor. At 1 year follow-up there was no recurrence.

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Jackson, C. Gary. "Glomus tympanicum and glomus jugulare tumors." Otolaryngologic Clinics of North America 34, no. 5 (2001): 941–70. http://dx.doi.org/10.1016/s0030-6665(05)70356-x.

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Bartels, Loren J., and Michael Gurucharri. "Pediatric Glomus Tumors." Otolaryngology–Head and Neck Surgery 99, no. 4 (1988): 392–95. http://dx.doi.org/10.1177/019459988809900407.

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Glomus tumors of the middle ear are unusual in adults, but exeedingly rare in children. While a dull, red bulging tympanic membrane in the adult may suggest a glomus tumor, it generally signifies infection in the child. This report details our management of a 10-year-old girl afflicted with bilateral chronic middle ear cleft infection that obscured bilateral glomus tumors. Review of the current English language literature reveals seven additional case reports of otologic glomus tumors in children less than fourteen years of age. Two additional cases are presented that were given to the senior author by personal communication, producing a total of 10 cases for review. Glomus tumors in children may be hidden by otitis media and appear more likely to be endocrine active. Failure to cure the lesion is apparent in five of six case reports of children with glomus jugulare tumors; three of these children are reported to have expired. Complete surgical extirpation is advocated for childhood glomus tumors.

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Vasilevska-Nikodinovska, Violeta, Milan Samardjiski, Rubens Jovanovik, Boro Ilievski, and Vesna Janevska. "Low-Grade Malignancy Glomus Tumor in a Setting of Multiple Glomus Tumors – Case Report." Open Access Macedonian Journal of Medical Sciences 7, no. 23 (2019): 4082–88. http://dx.doi.org/10.3889/oamjms.2019.610.

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BACKGROUND: Glomus tumors are rare neoplasms accounting for less than 2% of all soft tissue tumors but multiple lesions may be seen in up to 10% of the patients. Solitary glomus tumor (GT) most frequently appears as small nodule in specific locations such as subungual region or deep dermis. However, rarely these entities have been observed in extracutaneous locations such as the gastrointestinal, cardiovascular, respiratory tracts, and other visceral organs. A small fraction of the GTs may present as tumors of uncertain malignant potential or as malignant glomus tumors. CASE PRESENTATION: We report a patient with multiple glomus tumors on the time of diagnosis, which was histologically diagnosed as an atypical glomus tumor following resection of a tumor thrombus in the left renal vein, inferior vena cava trombus with intracardial extension, and mitral valve specimen. The intramuscular lesion from the thigh was diagnosed as a glomus tumor of uncertain malignant potential. Further examinations revealed multiple lesions trough her body: kidneys, breast, heart and subcutaneous tissue. The diagnosis of glomus tumor of uncertain malignant potential versus glomus tumor with low malignant potential could be quite challenging, and the clinical course may be as a determining factor for final diagnosis. CONCLUSION: To our knowledge, this is the only known case of glomus tumor with multiple organ involvement and aggressive biological behavior at presentation.

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Nthumba, Peter M., and Leahcaren Naguria Oundoh. "Glomus Tumors: A Systematic Review of the Sub-Saharan Africa Experience." Plastic and Reconstructive Surgery - Global Open 12, no. 2 (2024): e5564. http://dx.doi.org/10.1097/gox.0000000000005564.

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Background: Glomus tumors are rare benign tumors that were first described in 1812 by Wood. They arise from normal glomus apparatus, usually located in the reticular dermis of the body. Although glomus tumors are universal in occurrence, the sub-Saharan Africa experience has not been well documented. Methods: The authors performed a systematic literature review of eligible studies between 1960 and August 2023, using the terms “glomus,” “tumor,” “glomangioma,” “glomangiomyoma,” and “Africa.” We also performed a search of the AIC Kijabe Hospital pathology department database of about 140,000 records, covering 30 years, for the terms “glomus tumor,” “glomangioma” and “glomangiomyoma.” Results: The systematic literature search and institutional database search produced a total of 74 patients who had glomus tumors. These patients had a lag of between 3 months and 20 years from symptom development to definitive treatment. Conclusions: There are very few reports of glomus tumors from sub-Saharan Africa in the current literature: the authors’ histopathology database of 140,000 specimens had 46 glomus tumors (0.03%), and only 28 additional patients were found in literature from sub-Saharan Africa. The low numbers of African patients may indicate racial differences in the occurrence of glomus tumors, although this may also be due to failure of clinicians to recognize glomus tumors. The prolonged lag period between symptom development and definitive treatment for glomus tumors indicates the need for diligence in the diagnosis and treatment of a simple problem that is otherwise the cause of incapacitating pain and misery.

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Dissertations / Theses on the topic "Glomus tumors"

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Ehret, Felix [Verfasser], and Alexander [Akademischer Betreuer] Muacevic. "The role of image-guided robotic radiosurgery in the management of glomus jugulare tumors / Felix Ehret ; Betreuer: Alexander Muacevic." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2020. http://d-nb.info/1225682673/34.

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Loghmanieh, Siawasch [Verfasser], Wilhelm [Akademischer Betreuer] Sandmann, Andreas [Akademischer Betreuer] Saleh, and Dirk [Akademischer Betreuer] Grotemeyer. "Die chirurgische Therapie und Dignität des Glomus-caroticum-Tumors : retrospektive Untersuchung von Klinik, Diagnostik, Therapie und Verlauf von 36 Patienten / Siawasch Loghmanieh. Gutachter: Andreas Saleh. Betreuer: Wilhelm Sandmann ; Dirk Grotemeyer." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2011. http://d-nb.info/1015363857/34.

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URAKAWA, HIROSHI, HIROATSU NAKASHIMA, YOSHIHISA YAMADA, MIKITO TSUSHIMA, TAKEHIRO OHTA, and TOMOKO NISHIO. "INTRAOSSEOUS GLOMUS TUMOR OF THE ULNA: A CASE REPORT WITH RADIOGRAPHIC FINDINGS AND A REVIEW OF THE LITERATURE." Nagoya University School of Medicine, 2008. http://hdl.handle.net/2237/10551.

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Kinosada, Yasutomi, Hisatochi Maeda, Manabu Andoh, et al. "Tissue characterization by magnetization transfer ratio : Evaluate of the MTRs in breast tunors, globus pallidus and nasopharyngeal tumors." 日本医学放射線物理学会, 1997. http://hdl.handle.net/2237/19565.

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Vanti, Adriana Amorim. "Tumor glômico subungueal: estudo epidemiológico e retrospectivo, no período de 1991 a 2003." Universidade de São Paulo, 2004. http://www.teses.usp.br/teses/disponiveis/5/5133/tde-01102014-145503/.

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O tumor glômico é uma neoplasia benigna de células glômicas, de ocorrência incomum, observado como lesão solitária na falange distal dos quirodáctilos, representando de 1% a 4,5% das neoplasias das mãos. Foram estudados 20 casos de tumor glômico ocorridos no período de 1991 a 2003, nos ambulatórios de Dermatologia do Hospital das Clínicas e do Hospital do Servidor Público Municipal de São Paulo. Analisaram-se os prontuários, avaliando-se os aspectos epidemiológicos, clínicos e exames complementares, dando ênfase ao exame histopatológico e métodos de imagem. Os achados epidemiológicos deste estudo não diferiram significativamente do levantamento bibliográfico pesquisado, confirmando tratar-se de um tumor raro e pouco conhecido. A tríade clássica do tumor glômico \"dor paroxística, sensibilidade local e hipersensibilidade à alteração de temperatura\" esteve presente em 15 dos 20 casos examinados. Confirmou-se, na casuística analisada, a preferência pelos quirodáctilos e maior acometimento do sexo feminino. Histologicamente, os dados obtidos foram similares aos existentes na literatura, houve predominância do padrão arquitetural celular e a presença de cápsula tumoral, foi encontrada em apenas três casos. Os métodos de imagem não foram utilizados de maneira sistemática como auxiliares diagnóstico do tumor glômico, embora sejam de grande auxílio na confirmação e delimitação do tumor, especialmente a ressonância magnética que nesse estudo foi realizada em quatro dos 20 casos estudados, mostrando lesão evidente e não deixando dúvidas quanto ao diagnóstico. As recidivas, consideradas raras, ocorreram em 15% dos casos, por isso há a necessidade de um acompanhamento cirúrgico prolongado<br>The glomus tumor is a benign neoplasia of glomus cells, of uncommon occurrence, observed as a solitary lesion on distal phalanx of the chirodactyls, representing from 1% to 4,5% of the hand neoplasias. 20 cases of glomus tumor, occurred from 1991 to 2003, have been studied in the ambulatories of Dermatology of Hospital das Clínicas and of Hospital do Servidor Público Municipal of São Paulo. The medical registers had been analyzed and the epidemiologic and clinical aspects and complementary examination such as histopathologic examination and methods of images had been evaluated. The epidemiologic findings of this study did not differ significantly from the bibliographic research realized, confirming that it is an unfrequent and poorly studied tumor. The classical triad of glomus tumor symptoms: \"paroxysmal pain, local sensitivity and hypersensitivity to the fluctuation of temperature\" was present in 15 of the 20 studied cases. In the analyzed casuistry, the preference for chirodactyls and the greater number of manifestation on female sex had been confirmed. Histologically, the achieved data were similar to the ones presented in the literature, there was prevalence of the cellular architectural pattern and the presence of tumorous capsule was found in just 3 cases. The image methods were not used in a systematic way as a glomus tumor diagnosis aid, although they were a great help on the confirmation and delimitation of the tumor, especially the magnetic resonance imaging. The reincidences were considered sporadic and occurred in 15% of the studied cases, for this reason there is necessity of an extended surgical attendance

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Hemm, Simone. "Mise en concordance d'images sous cadre stéréotaxique : applications neurochirurgicales." Montpellier 1, 2005. http://www.theses.fr/2005MON1T010.

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Le progres en imagerie medicale met a la disposition des medecins un grand nombre d'informations. Leur combinaison exige un systeme de reference se deplacant avec le patient. Cette these demontre la faisabilite d'une methodologie utilisant le cadre stereotaxique de leksell, fixe sur le crane du patient et bloquant les mouvements de la tete. Dans l'intention d'ameliorer la prise en charge clinique des malades, il sert pour la mise en concordance d'images anatomiques avec des images : - anatomiques : verification de la position de l'electrode lors de la stimulation cerebrale profonde (irm pre- et postoperatoires), - theoriques : visualisation du volume stimule lors de la stimulation cerebrale profonde (irm, isolignes de champs electriques), - fonctionnelles : localisation et visee des sites d'hypermetabolisme lors des biopsies des tumeurs cerebrales (temp, irm). Les principes et la mise en oeuvre de cette generalisation du principe stereotaxique ainsi que les criteres du controle de qualite et les eventuelles sources d'erreurs sont discutes.

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Books on the topic "Glomus tumors"

1

Andel Gerhard Lourens van der Mey. Head and neck paragangliomas: A clinical genetic and pathological study of glomus tumors. s.n.], 1992.

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2

Sybert, Virginia P. Disorders of the Dermis. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780195397666.003.0005.

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Collagen – Ainhum – Amniotic Bands – Buschke-Ollendorff Syndrome – Dermatosparaxis – Ehlers-Danlos Syndromes – Ehlers-Danlos Types I, II, and III – Ehlers-Danlos Type IV – Ehlers-Danlos Type VI – Ehlers-Danlos Type VIII – Reactive Perforating Collagenosis – Elastin – Costello Syndrome – Cutis Laxa – Pseudoxanthoma Elasticum – Vascular – Ataxia Telangiectasia – Blue Rubber Bleb Nevus Syndrome – Cutis Marmorata Telangiectatica Congenita – Fabry Syndrome – Familial Flame Nevi – Hereditary Glomus Tumors – Hereditary Hemorrhagic Telangiectasia – Klippel-Trenaunay-Weber Syndrome – Maffucci Syndrome – Sturge-Weber Syndrome – Mixed – Aplasia Cutis Congenita – Focal Dermal Hypoplasia – Tuberous Sclerosis – Other Disorders of the Dermis – Albright Hereditary Osteodystrophy – Cutis Verticis Gyrata – Familial Dysautonomia – François Syndrome – Lipoid Proteinosis – Multiple Pterygia – Systemic Hyalinosis

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Sybert, Virginia P. Disorders of the Dermis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0005.

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Chapter 5 covers Collagen disorders (Ainhum, Amniotic Bands, Buschke-Ollendorff Syndrome, Dermatosparaxis), Ehlers-Danlos Syndromes (Ehlers-Danlos Types I, II, and III, Ehlers-Danlos Type IV, Ehlers-Danlos Type VI, Ehlers-Danlos Type VIII, and Reactive Perforating Collagenosis), Elastin (Costello Syndrome, Cutis Laxa, and Pseudoxanthoma Elasticum), Vascular disorders (Ataxia Telangiectasia, Cutis Marmorata Telangiectatica Congenita, Fabry Syndrome, Familial Flame Nevi, Hereditary Glomus Tumors, Hereditary Hemorrhagic Telangiectasia, Klippel-Trenaunay-Weber Syndrome, Maffucci Syndrome, and Sturge-Weber Syndrome, and Multiple Cutaneous and Mucosal Venous Malformations), Mixed disorders (Aplasia Cutis Congenita, Focal Dermal Hypoplasia, Tuberous Sclerosis Complex), and other Disorders of the Dermis (Albright Hereditary Osteodystrophy, Cutis Verticis Gyrata, Familial Dysautonomia, François Syndrome, Hyaline Fibromatosis Syndrome, Lipoid Proteinosis, and Multiple Pterygia). Each condition is discussed in detail, including dermatologic features, associated anomalies, histopathology, basic defect, treatment, mode of inheritance, prenatal diagnosis, and differential diagnosis.

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Sri-Ram, Kesavan, Anthony Mcgrath, Eric Yeung, et al. Benign tumours of soft tissues. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.002003.

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♦ Ganglion cyst♦ Intramuscular myxoma♦ Myositis ossificans♦ Nodular fasciitis♦ Haemangioma♦ Lipoma♦ Cavernous lymphangioma♦ Glomus tumour♦ Neurofibroma♦ Desmoid tumour♦ Elastofibroma♦ Schwannoma♦ Synovial chondromatosis.

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Book chapters on the topic "Glomus tumors"

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Hasson, Brian F., Brandon J. Fisher, Larry C. Daugherty, et al. "Glomus Tumors." In Encyclopedia of Radiation Oncology. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-540-85516-3_561.

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Yan, Jenny, and Kristin Janson Redmond. "Glomus Tumors." In Adult CNS Radiation Oncology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-42878-9_26.

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Lin, Timothy, Jenny Yan, and Kristin Janson Redmond. "Glomus Tumors." In Adult CNS Radiation Oncology. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-67878-3_26.

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Di Chiacchio, Nilton, Nilton Gioia Di Chiacchio, Robertha Carvalho de Nakamura, Michela Starace, Matilde Iorizzo, and Robert Baran. "Glomus Tumors." In Atlas of Nail Signs and Disorders with Clinical and Onychoscopic Correlation. CRC Press, 2024. http://dx.doi.org/10.1201/b22852-19.

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Timson, David J., Richard J. Reece, James B. Thoden, et al. "Glomus Tumors." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_8603.

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Morales, Sergio. "Glomus Tumor." In Bone Tumors. Springer London, 2021. http://dx.doi.org/10.1007/978-1-4471-7501-8_35.

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Kalil, Ricardo K. "Glomus Tumor." In Tumors and Tumor-Like Lesions of Bone. Springer London, 2015. http://dx.doi.org/10.1007/978-1-4471-6578-1_34.

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Zhang, Yaxia, and Andrew E. Rosenberg. "Glomus Tumor." In Tumors and Tumor-Like Lesions of Bone. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-28315-5_37.

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Mocellin, Simone. "Glomus Tumor." In Soft Tissue Tumors. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-58710-9_113.

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Schiffer, Davide, Maria Teresa Giordana, Alessandro Mauro, and Riccardo Soffietti. "Glomus Tumors, Paragangliomas." In Brain Tumors. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-60529-1_16.

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Conference papers on the topic "Glomus tumors"

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Messow, Helen Josephine, P. Mittmann, L. Decker, and R. Seidl. "Simultaneous appearance of subcranial intrajugulare Glomus tumors and hemangioma." In Abstract- und Posterband – 91. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Welche Qualität macht den Unterschied. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1710982.

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Halbartschlager, Simone, and Marc Bloching. "Endoscopic resection of Glomus Tympanicum tumors – a case series." In 95th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e. V., Bonn. Georg Thieme Verlag KG, 2024. http://dx.doi.org/10.1055/s-0044-1785000.

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Tatcheva, M., T. Struffert, and G. Wolf. "Komplizierter Verlauf bei der Therapie eines großen Glomus-Caroticum-Tumors." In Abstract- und Posterband – 91. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Welche Qualität macht den Unterschied. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1711529.

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Patel, Neil, Matthew Carlson, Bruce Pollock, et al. "Stereotactic Radiosurgery for Glomus Jugulare Tumors: Long-Term Tumor Control Using 3D Volumetric Tumor Analysis." In 29th Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1679516.

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Henry, Laura, James Naples, Jason Brant, et al. "Gamma Knife Stereotactic Radiosurgery Improves Pulsatile Tinnitus in Glomus Jugulare Tumors." In 29th Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1679609.

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Renson, A., J. Ilgner, M. Mull, M. Westhofen, and M. Wiesmann. "Preoperative diagnosis and management of recurring glomus tympanicum and jugulare tumors." In Abstract- und Posterband – 90. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Digitalisierung in der HNO-Heilkunde. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1686482.

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Hackenberg, S., R. Hagen, T. Meyer, and A. Scherzad. "Surgical therapy of glomus tympanicum and jugular tumors (GT) with the flexible CO2 laser." In Abstract- und Posterband – 91. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Welche Qualität macht den Unterschied. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1711306.

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Hackenberg, S., T. Meyer, A. Scherzad, et al. "Surgical therapy of glomus tympanicum and jugular tumors (GT) with the flexible CO2 laser." In 100 JAHRE DGHNO-KHC: WO KOMMEN WIR HER? WO STEHEN WIR? WO GEHEN WIR HIN? Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1728529.

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Kouhi, Ali, Ahmad Ameri, Sasan Dabiri, et al. "Comparison of Treatment Outcome in Patients with Glomus Jugular Tumors after Surgery and Radiotherapy." In Special Virtual Symposium of the North American Skull Base Society. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1725322.

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Daza-Ovalle, Alberto, L. Dade Lunsford, Ajay Niranjan, Othman Bim Alamer, and Zhishuo Wei. "Outcomes of Gamma Knife Radiosurgery for Glomus Jugulare Tumors: A 35-Year Single-Center Experience." In 32nd Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/s-0043-1762014.

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