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Journal articles on the topic 'Glomus tumour'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Sethu, C., and AU Sethu. "Glomus tumour." Annals of The Royal College of Surgeons of England 98, no. 1 (2016): e1-e2. http://dx.doi.org/10.1308/rcsann.2016.0005.

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Glomus tumours are rare tumours accounting for only 1–5% of soft tissue tumours of the hand. They are described classically in the subungual region. We present the case of a 32-year-old woman with a late diagnosis of a glomus tumour that had caused her excruciating pain. Clinical examination was positive for Hildreth’s sign and the Love test. Magnetic resonance imaging delineated the tumour, which was excised and confirmed histologically. This case highlights the continued delay in diagnosis of glomus tumours as well as the use of imaging in diagnosis and planning of surgery.

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2

Lee, Jun-Ku, Tae-sup Kim, Dong-won Kim, and Soo-Hong Han. "Multiple glomus tumours in multidigit nail bed." Handchirurgie · Mikrochirurgie · Plastische Chirurgie 49, no. 05 (2017): 321–25. http://dx.doi.org/10.1055/s-0043-115115.

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AbstractGlomus tumours are lesions of the glomus body. A solitary glomus tumour is a more common, characteristically painful lesion, frequently located under the nail, whereas multiple glomus tumours are a rare clinical and genetic entity. Multiple glomus tumours are rarely subungual and do not show preference for any particular region of the body. We report a rare case of painful multidigit subungual glomus tumours in both hands.A 34-year-old male patient complained of painful fingertips (right: thumb, index finger, long finger, and ring finger; left: thumb, long finger, ring finger, small fi

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3

Boyacioglu, Hatice, Nagihan Koc, Nihal Avcu, and Ozay Gokoz. "Glomus Tumour of the Lip Mimicking Squamous Cell Carcinoma - A Rare Case Report." Journal of Evolution of Medical and Dental Sciences 10, no. 9 (2021): 649–51. http://dx.doi.org/10.14260/jemds/2021/138.

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Glomus tumour is a rare soft tissue neoplasm arising from glomus body, which is in an arteriovenous anastomosis located particularly in the dermis. This tumour occurs most commonly in hands and feet, and is seldom found in other sites. The purpose of this report is to describe an unusual case of glomus tumour in the lip. A 17-year-old woman with a firm, painless and ulcerated lump in her lower lip was admitted to our clinic. Excisional biopsy was performed, and histopathological analysis revealed the lesion to be a subtype of glomus tumour called as a glomangioma. Most glomus tumours are benig

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4

Singh, Vikram, Vikas Kumar, Harkant Singh, and Nandita Kakkar. "Primary pulmonary glomus tumour: a diagnostic challenge." BMJ Case Reports 13, no. 2 (2020): e231926. http://dx.doi.org/10.1136/bcr-2019-231926.

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Glomus tumour is uncommon benign tumour, which derives from the glomus cells present around arteriovenous anastomosis. These tumours are found most commonly in the deep dermis of the extremities. Primary pulmonary glomus tumour is extremely rare and often misdiagnosed. Knowledge about the existence of glomus tumour in the lung, its classic histomorphology and judicious use of immunohistochemistry can help us in clinching the correct diagnosis.

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TAMER, Emine, Seray KÜLCÜ ÇAKMAK, Murat DEMİREL, and Ahmet Levent ALBAYRAK. "Glomus Tumour: Case Report." Turkiye Klinikleri Journal of Case Reports 24, no. 3 (2016): 274–77. http://dx.doi.org/10.5336/caserep.2015-48412.

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6

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, ai

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7

Santos, Leonardo D., Christopher Chow, and Alan R. Kennerson. "Glomus coccygeum may mimic glomus tumour." Pathology 34, no. 4 (2002): 339–43. http://dx.doi.org/10.1080/003130202760120508.

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8

Keir, J. A., M. Wilbourn, P. Anslow, and C. A. Milford. "Case report of glomus jugulare tumour associated with a posterior fossa cyst." Journal of Laryngology & Otology 123, no. 1 (2007): 126–28. http://dx.doi.org/10.1017/s0022215107001090.

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AbstractA subgroup of complex glomus jugulare tumours exists. This includes: multiple, giant or neuropeptide-secreting lesions; those associated with other lesions, such as dural arterio-venous malformation or an adrenal tumour; and tumours in which there has been previous treatment with adverse outcome. To our knowledge, we present the first case of a glomus jugulare tumour associated with a posterior fossa cyst. This entity should be included in the subgroup of complex glomus jugulare tumours.

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9

G, Sukanya, Geo Celestin Danny, Narayanan Baskaran, and Kavya Rajeev. "Ex vivo dermoscopy of extra digital glomus tumour." IP Indian Journal of Clinical and Experimental Dermatology 11, no. 1 (2025): 139–41. https://doi.org/10.18231/j.ijced.2025.022.

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Glomus tumour or glomangioma is an uncommon innocuous tumour of the skin. This painful tumour of skin is a vascular hamartoma arising from glomus cells and can be solitary or multiple, digital or extradigital. It is most commonly encountered in females in their 3 to 5 decade. Glomus tumour can occur anywhere in the body, subungual area being the most favoured site. Extradigital glomus tumour is extremely rare and can involve upper limb, legs or trunk. Pain, pin-point tenderness and cold sensitivity form the diagnostic triad of glomus tumour. The diagnosis of Glomus tumour is made after assessi

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10

Chim, Harvey, Amitabha Lahiri, and Winston Y. C. Chew. "ATYPICAL GLOMUS TUMOUR OF THE WRIST: A CASE REPORT." Hand Surgery 14, no. 02n03 (2009): 121–23. http://dx.doi.org/10.1142/s0218810409004347.

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Wrist glomus tumours are extremely rare. We report a case of an unusually large wrist glomus tumour with atypical presentation. Magnetic resonance imaging (MRI) findings correlated well to those previously described for digital glomus tumours. This rare differential should be considered when evaluating lesions around the wrist.

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11

Mathias, Rohini, Sharad Ramdas, and Renu G. Varghese. "Subungual Glomus Tumour." Our Dermatology Online 3, no. 2 (2012): 134–35. http://dx.doi.org/10.7241/ourd.20122.29.

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12

Arapantoni-Dadioti, P., J. Panayiotides, M. Fatsis, and G. Antypas. "Tracheal Glomus Tumour." Respiration 62, no. 3 (1995): 160–62. http://dx.doi.org/10.1159/000196414.

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13

TAKEI, T. R., and E. A. NALEBUFF. "Extradigital Glomus Tumour." Journal of Hand Surgery 20, no. 3 (1995): 409–12. http://dx.doi.org/10.1016/s0266-7681(05)80105-6.

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We report a case of an extradigital glomus tumour found in the forearm. A review of the literature suggests that extradigital glomus lesions in the upper limb may be more common than they are thought to be.

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14

Stajčić, Zoran, and Petar Bojić. "Intraoral glomus tumour." Journal of Cranio-Maxillofacial Surgery 15 (January 1987): 376–78. http://dx.doi.org/10.1016/s1010-5182(87)80087-2.

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15

Peretz, Eyal, Marcelo H. Grunwald, Ilana Avinoach, and Sima Halevy. "Solitary glomus tumour." Australasian Journal of Dermatology 40, no. 4 (1999): 226–27. http://dx.doi.org/10.1046/j.1440-0960.1999.00369.x.

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16

Rahman, Adam Tolulope, and Babatope Awosusi. "Extra-digital glomus tumour of the forehead: a case report of a solitary solid histopathologic subtype." Babcock University Medical Journal 7, no. 1 (2024): 132–37. http://dx.doi.org/10.38029/babcockuniv.med.j..v7i1.394.

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Background: Glomus tumours (GT) are benign neoplasms that develop from neuro-myoarterial structures known as “glomus bodies” involved in temperature and blood pressure control. GT rarely occur in the head and neck region, and the specific location of the glomus tumour on the forehead is even more uncommon. Case presentation: We report the case of a 36-year-old female who presented with painless swelling on the forehead of one year duration with a progressive increase in size. Physical examination showed a small forehead swelling with an initial clinical diagnosis of a sebaceous cyst. The patie

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17

González-Cámpora, Ricardo, José Luis Villar Rodríguez, Francisco Vázquez Ramírez, Salvador Díaz Cano, and Hugo Galera Ruiz. "Glomus tumour of the oropharynx." Journal of Laryngology & Otology 109, no. 1 (1995): 63–65. http://dx.doi.org/10.1017/s0022215100129263.

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AbstractHaemangiopericytoma and glomus tumours are infrequent neoplasms in otorrhinolaryngology. A case of glomus tumour with haemangiopericytomatous features of the left amygdalar fossa tsaeported. Its clinical, surgical and histological features are described. This case report supports the unitary concept of smooth muscle tumours of the small vascular wall.

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18

Seymour, F. K., S. Lloyd, and J. P. Harcourt. "Glomus jugulare tumour presenting with isolated accessory nerve palsy." Journal of Laryngology & Otology 118, no. 3 (2004): 234–36. http://dx.doi.org/10.1258/002221504322928053.

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Glomus tumours of the skull base are rare, and most frequently present with symptoms of hearing loss and tinnitus. Diagnosis is often delayed due to the slow growth of the tumour. We describe the previously unreported occurrence of a glomus tumour presenting with a unilateral accessory nerve palsy.

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19

International, Journal of Medical Science and Innovative Research (IJMSIR). "A Glomus Tumour of the Chest Wall Secondary to Bullet Injury – An Unusual Case with Review of Literature." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 4 (2024): 111–13. https://doi.org/10.5281/zenodo.15429631.

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<strong>Abstract</strong> Glomus tumour is a rare vascular tumour, the common site being subunguam. It is rarely seen on the chest wall region. Also, occurrence of glomus tumour after injury is very uncommon. We present a case of glomus tumour in a 76 year old male patient who presented with swelling on chest wall secondary to bullet injury and was clinically diagnosed as keloid. The case is presented to highlight its occurrence after injury as well as its rare presentation on chest wall.

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20

Brewis, C., I. D. Bottrill, S. B. Wharton, and D. A. Moffat. "Glomus jugulare tumour with metastases to cervical lymph nodes." Journal of Laryngology & Otology 114, no. 1 (2000): 67–69. http://dx.doi.org/10.1258/0022215001903726.

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Glomus jugulare tumours are classically described as benign tumours with a long time course often measured in decades. Although these tumours may be locally invasive, most cases are histologically benign and metastases are rare. The case of a malignant glomus jugulare tumour with a particularly aggressive pattern of spread is presented. At the time of surgery, which was within 12 months of the development of symptoms, intracranial spread and metastasis to cervical lymph nodes had already occurred, demonstrating that glomus jugulare tumours are not always benign.

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21

Stahl, Caleb, William G. Wong, Julie C. Fanburg-Smith, and Charles C. Vining. "Unsuspected gastric glomus tumour." BMJ Case Reports 16, no. 1 (2023): e253020. http://dx.doi.org/10.1136/bcr-2022-253020.

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Gastric glomus tumours (GGTs) are rare predominantly benign, mesenchymal neoplasms that commonly arise from the muscularis or submucosa of the gastric antrum and account for <1% of gastrointestinal soft-tissue tumours. Historically, GGT has been difficult to diagnose preoperatively due to the lack of unique clinical, endoscopic and CT features. We present a case of an incidentally identified GGT in an asymptomatic man that was initially considered a neuroendocrine tumour (NET) by preoperative fine-needle aspiration biopsy with focal synaptophysin reactivity. An elective robotic distal gastr

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22

AL-QATTAN, M. M., A. AL-NAMLA, A. AL-THUNAYAN, F. AL-SUBHI, and A. F. EL-SHAYEB. "Magnetic Resonance Imaging in the Diagnosis of Glomus Tumours of the Hand." Journal of Hand Surgery 30, no. 5 (2005): 535–40. http://dx.doi.org/10.1016/j.jhsb.2005.06.009.

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This paper studies the sensitivity, specificity and predictive values of MRI in the diagnosis of glomus tumours of the hand and investigates the final diagnosis and outcome in cases with false positive or negative imaging tests. A total of 42 cases with the clinical diagnosis of a glomus tumour were included in the study. All patients underwent MRI and the results of MRI were correlated with the final histological diagnosis of the excised lesion. MRI had a sensitivity of 90%, a specificity of 50%, a positive predictive value of 97% and a negative predictive value of 20%. The four cases in whic

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23

Yadav, Sandeep Kumar, Rajesh Kumar Rajnish, Vimal Prakash, and Vikrant Verma. "Glomus tumour located in the volar aspect of distal phalanx of thumb." BMJ Case Reports 17, no. 8 (2024): e260130. http://dx.doi.org/10.1136/bcr-2024-260130.

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A woman in her 40s presented with pain and tenderness over the volar aspect of distal phalanx of her thumb without any swelling or discolouration. MRI indicated a possible glomus tumour. The treatment involved complete excision, and histopathological examination of the excised tissue confirmed the diagnosis of a glomus tumour. Most reported cases of glomus tumours are usually located in either the subungual region or the tip of the finger. This case represents a rare presentation in an unusual location—the volar aspect of the distal phalanx of the thumb.

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24

Balatsouras, Dimitris G., Panayotis N. Eliopoulos, and Costas N. Economou. "Multiple glomus tumours." Journal of Laryngology & Otology 106, no. 6 (1992): 538–43. http://dx.doi.org/10.1017/s0022215100120080.

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AbstractA patient with multiple, synchronous, non-familial head and neck paragangliomas is reported. There were three primary neoplasms, a glomus tympanicum and glomus vagale on the right side and a glomus tumour of the carotid body on the left. Such a combination has never been reported previously.The reports of all the series with paragangliomas in the literature, as well as the reports of single cases with multiple tumours during the last three decades, are reviewed. Specific problems in diagnosis and management of multiple glomus tumours are discussed.

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25

Al-Ishaq, Z., U. Asif, M. Roy, O. Sikdar, A. Bhatnagar, and T. Sircar. "Glomus tumour of the nipple in a male patient." Annals of The Royal College of Surgeons of England 104, no. 3 (2022): e60-e63. http://dx.doi.org/10.1308/rcsann.2021.0141.

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A glomus tumour is a benign mesenchymal tumour. It is extremely rare in the breast. We report a case of glomus tumour of the nipple in a 54-year-old man. To the best of the authors' knowledge, this is the first case report of a glomus tumour of the nipple. We describe the different presenting symptoms, method of diagnosis and treatment.

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26

Rockall, T. A., J. C. Watkinson, S. E. M. Clark, and E. E. Douek. "Scintigraphic evaluation of glomus tumours." Journal of Laryngology & Otology 104, no. 1 (1990): 33–36. http://dx.doi.org/10.1017/s0022215100111727.

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AbstractThe current investigations of choice for a suspected glomus tumour are either direct or indirect angiography to include digital subtraction followed by computerized tomography (CT) or magnetic resonance imaging (MRI) or, if available, CT and MRI with gadolinium alone. Although these modalities confirm the diagnosis and give anatomical information to facilitate accurate staging, they do not provide functional data. The use of radionuclide scintigraphy can add an extra physiological dimension to glomus tumour imaging.Iodine-131/123 metaiodobenzylguanidine (MIBG) is a tumour imaging agent

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Connor, S. E. J., M. J. Gleeson, and E. Odell. "Extracranial glomus faciale tumour." Journal of Laryngology & Otology 122, no. 9 (2007): 986–89. http://dx.doi.org/10.1017/s0022215107000126.

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AbstractObjectives:To describe a unique presentation of a predominantly extracranial glomus faciale tumour. To discuss the role of imaging in the differential diagnosis and evaluation of a hypervascular parotid mass. To review the previous literature concerning the glomus faciale tumour.Case report:A 54-year-old woman presented with a six-month history of facial weakness, pain and a parotid mass. Ultrasound revealed a hypervascular parotid mass and pre-operative core biopsy suggested a paraganglioma. Computed tomography defined its deep extent and demonstrated involvement of the petrous tempor

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28

Kumar, Rajranjan. "The mysterious chronic finger pain- glomus tumour: a case report." International Surgery Journal 9, no. 6 (2022): 1262. http://dx.doi.org/10.18203/2349-2902.isj20221422.

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Glomus tumours are very rare, small, painful benign hamartomas, arising from the arterial end of the glomus body. Glomus tumors account for 1-2% of the soft tissue tumors in the hand. The exact etiopathogenesis is unknown. It is incapacitating to the patients because of chronicity of symptoms and lack of proper investigative tools to diagnose the tumor at an early stage. The clinical diagnosis was made on the basis of medical history and MRI findings. We report a case of glomus tumor in a 35-year-old female, situated in the pulp of distal phalanx of right middle finger, which was resected comp

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Tullie, Sebastian Thomas Edmund, Mohammed Kamil Quraishi, Thiwanka Karawita, and Salim Anjarwalla. "Rare presentation of a testicular glomus tumour." BMJ Case Reports 12, no. 11 (2019): e230935. http://dx.doi.org/10.1136/bcr-2019-230935.

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Glomus tumours are atypical in extracutaneous locations and very rarely located in reproductive organs. We present an unusual case of an incidentally discovered glomus tumour arising from the testis of a 47-year-old man. The testicular occurrence of this tumour type is not only exceptionally rare but also serves to highlight the debate regarding the optimal management of incidentally discovered small testicular lesions.

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Sangüesa, M. J., R. Fernández-Gabarda, and F. Cabanes Soriano. "Pre-patellar glomus tumour Tumor glómico prerrotuliano." Revista Española de Cirugía Ortopédica y Traumatología (English Edition) 54, no. 6 (2010): 411–12. http://dx.doi.org/10.1016/s1988-8856(10)70271-6.

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31

BHASKARANAND, K., and B. C. NAVADGI. "Glomus Tumour of the Hand." Journal of Hand Surgery 27, no. 3 (2002): 229–31. http://dx.doi.org/10.1054/jhsb.2001.0746.

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We report a series of 18 patients with pain in the thumb or finger tips who were diagnosed as having glomus tumour. Fourteen patients were found to have histopathologically proven glomus tumours, one had a neuroma and three had haemangioma. The duration of symptoms before treatment averaged 1.9 years. Cold-sensitivity and Hildreth’s tests have sensitivities of 100% and 77.4% respectively and specificity of 100%. Love’s pin test had a sensitivity of 100%. Love’s and Hildreth’s tests showed 78% accuracy, whereas the cold-sensitivity test was 100% accurate. We used a double-tourniquet technique d

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32

Sabzi, Feridoun, Aghigh Heydari, Mohammad Rouzbahani, Reza Heidari Moghaddam, and Atefeh Asadmobini. "Combination of cardiac and carotid glomus tumour: a rare case report." Folia Medica 64, no. 6 (2022): 1012–15. http://dx.doi.org/10.3897/folmed.64.e67448.

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The most common tumour of the heart is myxoma but paraganglioma (also called glomus tumour in extracardiac sites) in the cardiac position is the rarest of them. While this tumour accounts for 0.8% of all primary benign tumours, the combination of both neoplasms is an exceedingly rare occurrence. Herein, we present a case of combined carotid glomus tumour and left atrial paraganglioma tumour in which respiratory distress was the presenting symptom of cardiac type but carotid tumour was asymptomatic. The case underwent a two-step resection of the neck and cardiac mass with an uncomplicated posto

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Li, Lily, Victoria Bardsley, Andrew Grainger, and Phillip Johnston. "Extradigital glomangiomyoma of the forearm mimicking peripheral nerve sheath tumour and thrombosed varicose vein." BMJ Case Reports 14, no. 4 (2021): e241221. http://dx.doi.org/10.1136/bcr-2020-241221.

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Extradigital glomus tumour is uncommon, little-known outside of its subungual location, and may present without its classic triad of tenderness, cold sensitivity and paroxysmal pain. Imaging is non-specific and diagnosis is often delayed, sometimes for years, leading to unnecessary morbidity. Surgical excision is the treatment of choice, although technique depends on case specifics. Histological subtypes depend on the relative prominence of glomus cells, vascular structures and smooth muscle. The vast majority of glomus tumours are benign. We highlight the importance of considering extradigita

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Takata, Haruhiko, Yoshikazu Ikuta, Osamu Ishida, and Kenji Kimori. "TREATMENT OF SUBUNGUAL GLOMUS TUMOUR." Hand Surgery 06, no. 01 (2001): 25–27. http://dx.doi.org/10.1142/s0218810401000394.

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We reviewed 30 patients with subungual glomus tumours of the hand operated on between 1964 and 1997. Seven patients were male and 23 were female. Their age ranged from 16 to 78 years. A transungual approach was selected in 27 patients, and a periungual approach in three. Pre-operative pain subsided in all of the patients, but recurrence of the pain was observed in nine. Nail deformities were observed in nine patients before surgery. After surgery, it disappeared in three patients, persisted in six, and new deformities developed in five. To avoid recurrence of pain, it is important that the acc

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EKIN, A., M. ÖZKAN, and T. KABAKLIOGLU. "Subungual Glomus Tumours: A Different Approach to Diagnosis and Treatment." Journal of Hand Surgery 22, no. 2 (1997): 228–29. http://dx.doi.org/10.1016/s0266-7681(97)80069-1.

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Nine cases of subungual glomus tumour in which a transillumination test was used for diagnosis and a different operative technique was used to prevent postoperative nail deformity are described. The transillumination test is a new method for identifying a glomus tumour. With our surgical technique it is simple to approach a glomus tumour under the proximal nail bed and it produces a minimal defect.

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DAILIANA, Z. H., J. L. DRAPÉ, and D. LE VIET. "A Glomus Tumour with Four Recurrences." Journal of Hand Surgery 24, no. 1 (1999): 131–32. http://dx.doi.org/10.1054/jhsb.1998.0047.

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A case of a glomus tumour of the distal segment of the ring finger, with four apparent recurrences in an 8-year period, is described. The patient was treated by two different surgeons (two and three times respectively) and obtained pain free intervals of between 4 and 11 months before recurrence. Histological examination confirmed the diagnosis of a glomus tumour in all five procedures. The location of the glomus tumour was defined preoperatively by high resolution MR imaging.

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Herdman, Rory C. D., James E. Gillespie, and Richard T. Ramsden. "Facial palsy after glomus tumour embolization." Journal of Laryngology & Otology 107, no. 10 (1993): 963–66. http://dx.doi.org/10.1017/s0022215100124934.

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AbstractA case is presented of a patient undergoing pre-operative embolization of a glomus tumour who developed a facial palsy one hour after embolization. At the time of surgery it was found to be due to the embolization material (polyvinyl alcohol foam) blocking the stylomastoid artery. The blood supply of glomus tumours and the variations in the blood supply of the facial nerve are discussed.

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Lunn, Jessica, Jeremy Stanton, and Anand Arya. "Glomus tumour of the elbow: an unusual complication of surgery." Shoulder & Elbow 8, no. 3 (2016): 197–98. http://dx.doi.org/10.1177/1758573216640190.

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Glomus tumours of the elbow remain a challenge to diagnose correctly and efficiently. We present a case of a glomus tumour as a complication of elbow surgery. This has not been described previously. This case highlights the possibility of injury as a causative factor in these tumours and the difficulty in differentiating them from postoperative neuromas by clinical presentation and ultrasound imaging alone.

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Aslam, N., Z.-U.-S. Qazi, A. H. Ahmad, and R. U. Khan. "Malignant glomus tumour of larynx: first case report and literature review." Journal of Laryngology & Otology 126, no. 7 (2012): 743–46. http://dx.doi.org/10.1017/s0022215112000631.

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AbstractObjective:We describe the first reported case of a malignant glomus tumour of the larynx.Method:Case report and review of the world literature concerning malignant glomus tumours.Results:A 37-year-old man presented with progressive hoarseness and dyspnoea. A smooth, right-sided laryngeal mass was found on flexible nasolaryngoscopy. Initial biopsy of this lesion was reported as a true ‘glomus tumour’, which is a benign lesion. Wide local excision was performed. The final histology of this specimen showed it to be a ‘malignant glomus tumour’. Immunohistochemistry was positive for smooth

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Kouzaki, H., J. Fukui, and T. Shimizu. "Management of a catecholamine-secreting tympanicum glomus tumour: case report." Journal of Laryngology & Otology 122, no. 12 (2008): 1377–80. http://dx.doi.org/10.1017/s0022215108001801.

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AbstractObjective:To report the safe management and treatment of a catecholamine-secreting tympanicum glomus tumour.Case report:A 73-year-old women presented with a catecholamine-producing glomus tympanicum tumour, complaining of hearing impairment and left ear pain. Physical examination revealed a red, pulsating swelling in the left tympanic membrane. Computed tomography demonstrated a soft tissue mass filling the entire middle-ear cavity and a partial osteolytic lesion in the internal carotid artery. Angiographic examination revealed a densely contrasting tumour with feeding vessels from the

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Izadi, S., P. D. Karkos, R. Krishnan, J. Hsuan, and T. H. J. Lesser. "Papilloedema secondary to venous sinus thrombosis following glomus jugulare tumour surgery." Journal of Laryngology & Otology 123, no. 12 (2009): 1393–95. http://dx.doi.org/10.1017/s0022215109005477.

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AbstractObjective:We present a case of a patient who had undergone embolisation and resection of a left glomus jugulare tumour, who presented three weeks post-operatively with magnetic resonance venography confirmed symptomatic cerebral venous sinus thrombosis.Method:We present a case report and a review of the world literature concerning glomus jugulare tumours and cerebral venous sinus thrombosis.Case report:A 42-year-old man presented with blurred vision and reduced Snellen visual acuity just three weeks after glomus jugulare tumour surgery. Fundoscopy revealed bilateral haemorrhagic optic

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AL-QATTAN, M. M., and H. M. CLARKE. "An Isolated Granular Cell Tumour of the Thumb Pulp Clinically Mimicking a Glomus Tumour." Journal of Hand Surgery 19, no. 4 (1994): 420–21. http://dx.doi.org/10.1016/0266-7681(94)90201-1.

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A rare case of an isolated granular cell tumour of the thumb pulp clinically mimicking a glomus tumour is described. The rationale behind performing oestrogen receptor staining for granular cell tumours is discussed.

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Khan, Salma, Hussain Jan Abbasi, and Atiq Ur Rehman. "Glomus tumour of the hand: a case report and review of the literature." Journal of Rehman Medical Institute 7, no. 3 (2021): 26–27. http://dx.doi.org/10.52442/jrmi.v7i3.358.

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Glomus tumours are uncommon benign lesions, constituting 1-5% of all soft tissue neoplasia of the hands. It was first described in 1812 by Wood as painful subcutaneous nodules. The most common site for this tumour is subungual region and affects females more frequently than males. It commonly presents as pain and pinpoint tenderness and cold sensitivity. Being a rare tumour, its diagnosis is often delayed and cause undue anxiety to the patients. We present a case a of left index finger glomus tumour, which remained undiagnosed for many years, after being seen by multiple clinicians.

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Robinson, Philip J., Henry R. Grant, and Stephen G. Bown. "NdYAG laser treatment of a glomus tympanicum tumour." Journal of Laryngology & Otology 107, no. 3 (1993): 236–37. http://dx.doi.org/10.1017/s0022215100122728.

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Glomus tympanicum tumours are highly vascular tumours of the middle ear. Their removal by conventional surgical methods requires an extensive procedure in many cases, often with ossicular disarticulation to allow adequate exposure prior to the ‘chaotic’ and haemorrhagic event of tumour removal. This paper reports on the use of an NdYAG laser in a case of a large glomus tympanicum tumour. The laser facilitated a transcanal approach, avoided ossicular disarticulation and allowed accurate and almost bloodless ablation of the entire tumour.The NdYAG laser appears to be a very useful treatment moda

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Sharma, S. P., Y. C. Yadav, A. K. Agarwal, O. P. Singh, and R. K. Misra. "Glomus tumour of the nose." Indian Journal of Otolaryngology 37, no. 2 (1985): 61. http://dx.doi.org/10.1007/bf03047626.

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Massey, E. W. "Shoulder pain from glomus tumour." Journal of Neurology, Neurosurgery & Psychiatry 55, no. 5 (1992): 413–14. http://dx.doi.org/10.1136/jnnp.55.5.413-b.

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Lim, KAS, MF Borg, M. Schultz, M. Rice, and AE Potter. "Glomus tumour in a child." Australasian Radiology 49, no. 6 (2005): 516–18. http://dx.doi.org/10.1111/j.1440-1673.2005.01505.x.

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SHEFFIELD, E., A. DEWAR, B. CORRIN, B. J. ADDIS, and B. CONROY. "Glomus tumour of the trachea." Histopathology 13, no. 2 (1988): 234–36. http://dx.doi.org/10.1111/j.1365-2559.1988.tb02032.x.

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SUNDERRAJ, S., A. A. AL-KHALIFA, A. K. PAL, H. P. PIM, and S. H. SABRI. "Primary intra-osseous glomus tumour." Histopathology 14, no. 5 (1989): 532–36. http://dx.doi.org/10.1111/j.1365-2559.1989.tb02191.x.

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Binesh, F., A. Akhavan, S. T. Zahir, and T. R. Bovanlu. "Clinically malignant atypical glomus tumour." Case Reports 2013, jan03 1 (2013): bcr2012007618. http://dx.doi.org/10.1136/bcr-2012-007618.

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