Search results for "paraganglioma"
showing 10 items of 23 documents
Malignant carotid paraganglioma: A case report
2019
Tumors of the carotid body are uncommon neoplasms that originate in the neuroectoderm. These tumors are slow growing but well vascularized and very destructive. Between 5% and 13% of carotid body tumors are malignant, behaving aggressively at the local level, invading the adjacent lymph nodes, and resulting in remote metastases. We present the case of a 60-year-old man who was examined for pain and paresthesias in his arm. Magnetic resonance imaging showed a large tumor in the left carotid space. Histologic study of a biopsy specimen from the tumor revealed that it was a paraganglioma. Further studies to determine the extent of disease detected metastases in bone and lung, confirming the tu…
Hearing results after hypotympanotomy for glomus tympanicum tumors.
2011
We postulate, that glomus tympanicum tumors (GTTs) may be safely removed without interference with the ossicular chain via a hypotympanotomy approach.Prospective, nonrandomized anatomic and clinical study.Tertiary referral center.All 17 patients between 1989 and 2009 with GTTs without involvement of the lumen of the jugular bulb.We used a modified hypotympanotomy approach. Our technique is a modification of the one first published by Shambaugh (1955). Pure-tone audiograms were performed in all patients. Preoperative and postoperative audiograms were modeled in a linear mixed model evaluating hearing threshold for air and bone conduction and air-bone gap at 500, 1,000, 2,000, and 3,000 Hz. I…
Miega artērijas audzēju ķirurģiska ārstēšana Latvijā no 2010. līdz 2015.gadam
2016
Ievads: Miega artēriju audzēji (MAA) ir reti, lēni augoši un labi apasiņoti neiroendokrīni veidojumi, kuru izcelsme ir miega artērijas bifurkācijas līmenī esošās paraganglionārās šūnas. Mērķis: Pētījuma mērķis bija izpētīt MAA pacientus Latvijā pēdējo piecu gadu laikā, veicot demogrāfisku, kā arī ārstēšanās iznākumu analīzi. Materiāli un metodes: Tika veikta retrospektīva analīze, caurskatot pacientu slimības vēstures no 2010. līdz 2015. gadam Paula Stradiņa Klīniskās Universitātes slimnīcā, kurā esošais asinsvadu ķirurģijas centrs ir vadošais Latvijā, kurā ārstē MAA. Pētījuma ietvaros pacienti tika arī uzaicināti uz duplex ultrasonogrāfiju apsekošanai. Rezultāti: Kopumā 10 pacientiem tika …
Congenital Plaque-Type Glomuvenous Malformations Associated with Fetal Pleural Effusion and Ascites
2010
Glomuvenous malformations are hereditary vascular anomalies, usually without extracutaneous involvement. We report two cases of extensive thoracic plaque-type glomuvenous malformation in newborns who had previously been diagnosed in utero with pleural effusion and ascites, suggesting a pathogenic link between the two conditions.
Szintigraphie adrenerger Tumoren mit 131J-meta-Benzylguanidin
2008
Pheochromocytoma scanning using 131J-meta-benzylguanidine was done in one patient with metastasizing paraganglioma, one patient with multiple endocrine neoplasia type IIb. No activity of tumour tissue could be demonstrated in the patient with metastasizing paraganglioma, whereas the pheochromocytoma could be clearly defined in the patient with multiple endocrine neoplasia type IIa. The female with multiple endocrine neoplasia type IIb showed a suspect space-occupying lesion of the left adrenal using computed tomography. Pheochromocytoma could be excluded by 131J-benzylguanidine scanning, selective estimation of catecholamines in adrenal venous blood as well as the glucagon stimulation and c…
Follicular adenoma in ectopic thyroid. A case-report
2017
Highlights • Ectopic thyroid is thyroidal tissue located far from its anatomic place. • A patient under our observation displayed left submandibular swelling. • The FNAC test report described a follicular adenoma. • Based on the FNAC diagnosis, we surgically removed the mass. • The post-operative follow-up was uneventful.
Intraoperative Scintigraphy With Portable Gamma Camera for the Localization of Interaortocaval Paraganglioma
2021
A 15-year-old adolescent girl diagnosed of interaortocaval paraganglioma with a positive 123I-MIGB SPECT/CT and 1 unsuccessful prior surgery was operated on with the assistance of a handheld gamma camera. Once the lesion was located and removed, 2 images were taken, one of the surgical field (without 123I-MIGB uptake) and another of the tumor ex vivo (with high 123I-MIGB uptake), confirming that the lesion had been satisfactorily excised. This case highlights the use of a portable gamma camera as a useful tool to locate this rare tumor, with a SPECT/CT positive for 123I-MIGB and a difficult anatomical location suspected.
Emerging Therapies in Pheochromocytoma and Paraganglioma: Immune Checkpoint Inhibitors in the Starting Blocks
2021
Pheochromocytoma and paraganglioma are neuroendocrine neoplasms, originating in the adrenal medulla and in parasympathetic and sympathetic autonomic nervous system ganglia, respectively. They usually present as localized tumours curable with surgery. However, these tumours may exhibit heterogeneous clinical course, ranging from no/minimal progression to aggressive (progressive/metastatic) behavior. For this setting of patients, current therapies are unsatisfactory. Immune checkpoint inhibitors have shown outstanding results for several types of solid cancers. We therefore aimed to summarize and discuss available data on efficacy and safety of current FDA-approved immune checkpoint inhibitor…
Imaging of cervical lymph node metastases in malignant jugular paraganglioma: Imaging of paraganglioma metastases
2009
Not available
6-18F-Fluoro-l-Dihydroxyphenylalanine Positron Emission Tomography Is Superior to123I-Metaiodobenzyl-Guanidine Scintigraphy in the Detection of Extra…
2010
Context: Pheochromocytomas (PHEOs) and paragangliomas (PGLs) may be better detected by 18F-fluorodihydroxyphenylalanine-positron emission tomography (FDOPA-PET) than 123I-metaiodobenzyl-guanidine (123-I-MIBG) scintigraphy. Objective: The objective of the study was to correlate functional imaging results with immunohistochemical, molecular-genetic, and biochemical findings. Design and Setting: Thirty consecutive patients with suspected PHEO/PGL presenting at a tertiary referral centre were investigated in a prospective study. Patients: Twenty-five patients had confirmed PHEO/PGL. Thirteen of 25 patients had a hereditary PHEO/PGL syndrome (two multiple endocrine neoplasia II, six succinate de…