Systemic Radiopharmaceutical Therapy of Pheochromocytoma and Paraganglioma
Whereas benign pheochromocytomas and paragangliomas are often successfully cured by surgical resection, treatment of metastatic disease can be challenging in terms of both disease control and symptom control.
J. Carrasquillo +5 more
semanticscholar +1 more source
Magnetic resonance and computed tomography imaging of a carotid body tumor in a dog [PDF]
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
Mediastinal Paraganglioma [PDF]
Paragangliomas of the mediastinum are rare, with only approximately 150 cases reported in the literature. Surgical excision is the treatment of choice; however, these tumors often lie near critical vascular structures. Here we present the case of a patient with a mediastinal paraganglioma discovered during a diagnostic procedure.
Stephanie N, Buchanan +2 more
openaire +2 more sources
Succinate dehydrogenase (SDH)-deficient renal carcinoma:a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients [PDF]
Succinate dehydrogenase (SDH)-deficient renal carcinoma has been accepted as a provisional entity in the 2013 International Society of Urological Pathology Vancouver Classification.
Belinsky +46 more
core +4 more sources
Post-Transcriptional Dysregulation by miRNAs Is Implicated in the Pathogenesis of Gastrointestinal Stromal Tumor [GIST] [PDF]
peer-reviewedIn contrast to adult mutant gastrointestinal stromal tumors [GISTs], pediatric/wild-type GISTs remain poorly understood overall, given their lack of oncogenic activating tyrosine kinase mutations.
Hans-Ulrich Schildhaus +12 more
core +5 more sources
Vertigo as the sole complaint of tympanomastoid paraganglioma
Background: Tympanomastoid paragangliomas are usually benign, slowly growing, painless tumors. The common presenting symptoms of this tumor are pulsatile tinnitus and conductive hearing loss.
Xi-Xing Li, Wei-Na Cui, Guo-Dong Gao
doaj +1 more source
A case report of bladder paraganglioma and literature review
Bladder paraganglioma is a rare tumor originated from the chromaffin cells of the bladder. We discuss a case of a 49-year-old male patient with bladder paraganglioma, including the clinical and ultrasonographic features, the histopathological and ...
Xiang Ji, MD, Xia Zhang, MD
doaj +1 more source
Routine genetic screening with a multi-gene panel in patients with pheochromocytomas [PDF]
PURPOSE: Several new gene mutations have been reported in recent years to be associated with a risk of familial pheochromocytoma. However, it is unclear as to whether extensive genetic testing is required in all patients. METHODS: The clinical data
Cranston, Treena +8 more
core +1 more source
Transcanal endoscopic excision of tympanic paraganglioma: A three-case series
Paragangliomas are rare neuroendocrine tumors that arise in sympathetic and parasympathetic paraganglion system, derived from neural crest cells. Tympanic paraganglioma is a type of head and neck paraganglioma involving the middle ear cleft.
Satish Nair +3 more
doaj +1 more source
Prediction of inherited genomic susceptibility to 20 common cancer types by a supervised machine-learning method. [PDF]
Prevention and early intervention are the most effective ways of avoiding or minimizing psychological, physical, and financial suffering from cancer. However, such proactive action requires the ability to predict the individual's susceptibility to cancer
Kim, Byung-Ju, Kim, Sung-Hou
core +2 more sources

