Results 91 to 100 of about 34,897 (270)
Journal of Medical Case Reports, 2019 Background Neurofibromatosis type 1 has a higher prevalence of pheochromocytoma and paraganglioma than the general population: 1.0–5.7% versus 0.2–0.6%.
Juan Wang +3 more
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Új módszertani lehetőségek és ezek alkalmazása a hormonális rendszer daganatainak genetikai kivizsgálásában [PDF]
, 2015 The technical developments leading to revolution in clinical genetic testing offer new approaches for patients with cancer. From one mutation or one gene approach the scale of genetic testing moved to whole exome or whole genome scale.
Baghy K, +4 more
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Primary hyperparathyroidism in a domestic shorthair cat following I131 radioiodine therapy
Journal of Small Animal Practice, EarlyView.A 12‐year‐old male neutered domestic shorthaired cat presented for further assessment of a cervical mass, having undergone radioiodine therapy for treatment of hyperthyroidism 2 years prior to presentation. Initial cytological diagnosis of the mass was supportive of a carcinoma and laboratory results were consistent with primary hyperparathyroidism ...
E. Ruane +3 more
wiley +1 more source
Case Reports in Endocrinology, 2014 Pheochromocytoma and paraganglioma are rare in the pediatric population occurring in approximately 1 in 50,000 children. While some cases are sporadic, they have commonly been associated with syndromes such as von Hippel-Lindau, multiple endocrine ...
Heather Choat +4 more
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Robot assisted laparoscopic excision of a paraganglioma: new therapeutic approach
International Brazilian Journal of Urology, 2014 The Paraganglioma is the most common extra-adrenal pheochromocytoma arising from neural crest (1) (It will better to write: The paraganglioma is an extra-adrenal pheocromocytoma arising from the neural crest. 10% of pheocromocytomas are extra-adrenal and
G. Cochetti +6 more
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Rapid-sequence MRI for long-term surveillance for paraganglioma and phaeochromocytoma in patients with succinate dehydrogenase (SDHx) mutations [PDF]
, 2016 INTRODUCTION: Patients with SDHx mutations need long-term radiological surveillance for the development of paragangliomas and phaeochromocytomas, but no longitudinal data exist.
Bull, M. +3 more
core +1 more source
Pathology International, EarlyView.Histopathological and immunohistochemical findings from the excisional biopsy of a right parapharyngeal mass in a 56‐year‐old woman with follicular dendritic cell sarcoma arising in Castleman disease. (A) H&E staining reveals atypical tumor cells intimately admixed with lymphocytes. (B) Adjacent areas show “lollipop lesions” characteristic of Castleman
Shunsuke Koga +3 more
wiley +1 more source
A case report of bladder paraganglioma and literature review
Radiology Case Reports, 2022 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
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Beyond fluorodeoxyglucose: Molecular imaging of cancer in precision medicine
CA: A Cancer Journal for Clinicians, EarlyView.Abstract Cancer molecular imaging is the noninvasive visualization of a process unique to or altered in neoplasia, such as proliferation, glucose metabolism, and receptor expression, which is relevant to patient management. Several molecular imaging modalities are now available, including magnetic resonance, optical, and nuclear imaging.
Malik E. Juweid +6 more
wiley +1 more source
Transcanal endoscopic excision of tympanic paraganglioma: A three-case series
Laparoscopic, Endoscopic and Robotic Surgery, 2020 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
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