Results 41 to 50 of about 9,672 (223)

Symplastic glomus tumor [PDF]

open access: yesTurkish Journal of Pathology, 2013
Glomus tumors showing nuclear pleomorphism without any other malignant features have been defined as symplastic glomus tumors. This type of glomus tumor is rarely encountered. Another case of symplastic glomus tumor is described in this study. A 37-year-old woman referred to the hospital with the complaint of a palpable tender nodule on the fourth ...
Fevziye, Kabukçuoğlu   +3 more
openaire   +2 more sources

Gastric glomus tumor [PDF]

open access: yesJournal of Surgical Case Reports, 2016
Gastric glomus tumors are rare, mesenchymal neoplasms, generally described as benign and account for nearly 1% of all gastrointestinal soft tissue tumors. The most common gastrointestinal site of involvement is the stomach, particularly the antrum. Gastric glomus tumors are submucosal tumors that lack specific clinical and endoscopic characteristics ...
Papadelis, Alexandria   +2 more
openaire   +2 more sources

Glomus Tumor on the Volar Aspect of the Distal Phalanx, an Unusual Presentation for an Unusual Neoplasm‎: A Case Report

open access: yesJournal of Orthopedic and Spine Trauma, 2020
Background: In the fingertips, the glomus tumors usually involve the subungual areas with typical triad symptoms including pain, tenderness to palpation, and cold sensitivity. The glomus tumor of volar aspect of digits is rare.
Sam Hajialiloo Sami   +2 more
doaj   +1 more source

Glomus tumor of the crissum: A case report and review of literature

open access: yesIndian Journal of Pathology and Microbiology, 2022
Glomus tumor is a rare mesenchymal neoplasm arising from the modified smooth muscle cells of the glomus body. Primary crissum glomus tumor is extremely rare without any published in the literature.
Yuanyin Zheng   +3 more
doaj   +1 more source

Minimally invasive resection of a glomus tumor of the thoracic spine: a case report and literature review

open access: yesJournal of International Medical Research, 2019
Objective Spinal involvement of glomus tumors is extremely rare. We herein present a case of a spinal glomus tumor and reviewed the literature to identify the most effective surgical treatment of spinal glomus tumors.
Zhiwei Liao   +3 more
doaj   +1 more source

Glomus tumor of penis- A rare case [PDF]

open access: yes, 2013
Glomus tumors are rare, painful, and benign soft tissue tumors of the skin arising from the glomus body, an arteriovenous thermoregulatory structure. This lesion is usually found on the extremities.
Madhuri S. Kate   +2 more
core  

Magnetic resonance and computed tomography imaging of a carotid body tumor in a dog [PDF]

open access: yes, 2012
A 5-year-old castrated male Labrador Retriever was presented to a referring veterinarian for a swelling in the neck region. Based on the results of histopathology, a carotid body tumor, was diagnosed.
De Cock, Hilde   +4 more
core   +2 more sources

How I Do It: A Stepwise Surgical Technique for Fisch Class B Glomus Tympanicum

open access: yesThe Laryngoscope, EarlyView.
We describe a stepwise retroauricular microsurgical workflow for bulky tympanic paragangliomas, combining circumferential canaloplasty with temporary removal and replacement of the tympanomeatal flap and malleus to optimize exposure and bleeding control.
Stéphane Gargula   +8 more
wiley   +1 more source

Diagnosis and treatment of carotid body paraganglioma: 21 years of experience at a clinical center of Serbia [PDF]

open access: yes, 2005
Background The carotid body paraganglioma (chemodectoma) is a relatively rare neoplasm of obscure origin. These are usually benign and commonly present as asymptomatic cervical mass.
Lazar B Davidovic   +4 more
core   +1 more source

Natural History and Management of Familial Paraganglioma Syndrome Type 1: Long-Term Data from a Large Family [PDF]

open access: yes, 2020
Head and neck paragangliomas are the most common clinical features of familial paraganglioma syndrome type 1 caused by succinate dehydrogenase complex subunit D (SDHD) mutation. The clinical management of this syndrome is still unclear.
Cantisani, Vito   +12 more
core   +1 more source

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