Results 21 to 30 of about 51,236 (315)

Paraurachal paraganglioma

open access: yesIJU Case Reports, 2022
IntroductionParagangliomas (PGLs) are frequently reported around the abdominal aorta; however, are extremely rare near the urachus.Case presentationA 78‐year‐old woman was referred to the urology department of our hospital for further examination and treatment of a 1.2‐cm tumor in the lower abdominal wall, a tumor excision was then performed.
Masafumi Tsuruta   +9 more
openaire   +3 more sources

Vagal Paraganglioma [PDF]

open access: yesSkull Base, 2006
To report the outcomes of surgical treatment of vagal paragangliomas and to define a management protocol.A retrospective case series.Sixteen consecutive patients with vagal paragangliomas managed by surgical resection using a cervicoparotid approach and pericapsular dissection using microsurgical techniques between 1990 and 2003.All patients either had
Zanoletti, Elisabetta, Mazzoni, Antonio
openaire   +3 more sources

Paraganglioma in the nasopharynx [PDF]

open access: yesIndian Journal of Otolaryngology and Head and Neck Surgery, 1996
A 50-year old male presented with swollen right eyelids, bleeding per nostrils and a vague left post-auricular swelling for 4 months. Posterior rhinoscopy revealed one pinkish polypoidal mass in the posterior nare and roof of nasopharynx. FNAC from the post-auricular swelling suggested metastatic undifferentiated carcinoma.
Kaushik Debnath   +4 more
openaire   +3 more sources

Succinate dehydrogenase‐deficient malignant paraganglioma complicated by succinate dehydrogenase‐deficient renal cell carcinoma

open access: yesIJU Case Reports, 2022
Introduction SDH Gene mutation is known to be a common cause of pheochromocytoma/paraganglioma and renal cell carcinoma. Here, we report a case of succinate dehydrogenase B‐deficient paraganglioma, which has a high risk of metastasis and recurrence ...
Yoshitomo Yamaguchi   +9 more
doaj   +1 more source

Systemic Radiopharmaceutical Therapy of Pheochromocytoma and Paraganglioma

open access: yesJournal of Nuclear Medicine, 2021
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

European multicentre study on outcome of surgery for sporadic primary hyperparathyroidism

open access: yesBJS (British Journal of Surgery), EarlyView., 2020
Some 5861 patients undergoing first‐time surgery for sporadic primary hyperparathyroidism were registered in the Eurocrine® database between 2015 and 2018. The use of intraoperative parathyroid hormone measurement decreased the risk of conversion and persistent hypercalcaemia.
A. Bergenfelz   +3 more
wiley   +1 more source

Unrecognised adrenergic symptoms and the delayed diagnosis of urinary bladder paraganglioma [PDF]

open access: yesVojnosanitetski Pregled, 2015
Introduction. Paraganglioma is a rare neuroendocrine neoplasm that may arise from the extra-adrenal autonomic paraganglia. Urinary bladder paraganglioma is typically presented as repeated episodes of palpitations, headache or blood pressure rise
Dragović Tamara   +6 more
doaj   +1 more source

Adrenocorticotropic Hormone-Producing Paraganglioma With Low Plasma ACTH Level: A Case Report and Review of the Literature

open access: yesFrontiers in Endocrinology, 2020
Ectopic adrenocorticotropic hormone (ACTH) syndrome caused by paraganglioma is extremely rare. It usually accompanied by high or normal plasma ACTH level.
Siyue Liu   +4 more
doaj   +1 more source

An Extra-adrenal Pheochromocytoma Presenting as Malignant Hypertension-A Report of two cases [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2013
Malignant hypertension is a complication of hypertension characterized by elevated blood pressure (200mm/140mm Hg), is considered a medical emergency and is rarely secondary to paraganglioma.
Mahesh Kumar U   +4 more
doaj   +1 more source

Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.

open access: yesJournal of Clinical Endocrinology and Metabolism, 2014
OBJECTIVE The aim was to formulate clinical practice guidelines for pheochromocytoma and paraganglioma (PPGL). PARTICIPANTS The Task Force included a chair selected by the Endocrine Society Clinical Guidelines Subcommittee (CGS), seven experts in the ...
J. Lenders   +8 more
semanticscholar   +1 more source

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