Výsledky vyhledávání - "Octreotide scan"

Primary thoracic gastrinoma causing Zollinger-Ellison syndrome

Autor: Amir Ghasemloee, Behnaz Jahanbin, Shahab Rafieian, Matin Vahedi

Publikováno v: Indian J Thorac Cardiovasc Surg

Gastrinomas are located largely in the pancreaticoduodenal region. However, gastrinomas have also been found in non-pancreaticoduodenal regions. Our study is a rare report of gastrinomas within the thoracic cavity. A 53-year-old male patient presente

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8066bdc2d33f9f39c5a18e7ed669cea
https://doi.org/10.1007/s12055-021-01211-3

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A rare case of ectopic ACTH syndrome caused by primary renal neuroendocrine tumor

Autor: Paweena Chunharojrith, Kanapon Pradniwat, Tanawan Kongmalai

Publikováno v: Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2021)
Endocrinology, Diabetes & Metabolism Case Reports

Summary Ectopic adrenocorticotropic hormone (ACTH) secretion is responsible for 5–15% of Cushing’s syndrome (CS). Neuroendocrine tumor (NET) is a common cause of ectopic ACTH syndrome (EAS). However, primary renal NET is exceedingly rare. Fewer t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22d867357b845c6e32ee8402a60cad96
https://edm.bioscientifica.com/view/journals/edm/2021/1/EDM20-0076.xml

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Large cell neuroendocrine carcinoma in the unusual location of the descending colon

Autor: Jin-whan Cha, Alan Mo, Millet Yang

Publikováno v: Radiology Case Reports, Vol 15, Iss 10, Pp 1841-1844 (2020)
Radiology Case Reports

Neuroendocrine neoplasms are most often found in the small intestine, rectum, appendix, and stomach. The colon, excluding the appendix and the cecum, is a rare location for these neoplasms and often gives rise to highly proliferative, poorly differen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35747788c478ea59aa71b95a86412e10
https://doi.org/10.1016/j.radcr.2020.07.045

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Intravial or In Vivo Production of 99mTc-Dextrose Complexes May Play a Role in Altering Biodistribution of 99mTc-HYNIC-Octreotide Scan

Autor: Babak Shafiei, Mohsen Qutbi, Isa Neshandar Asli

Publikováno v: Clinical nuclear medicine. 46(10)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e8761eabf3e6e05874fef1eef1d8148
https://pubmed.ncbi.nlm.nih.gov/34477603

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Imaging and Diagnostic Challenges in a Patient With Refractory Hypoglycemia Caused by Insulinomas Related to Multiple Endocrine Neoplasia Type 1

Autor: Michael E. Nance, Ritika Verma, Cory DeClue, Tarang Patel, Mark Reed

Publikováno v: Cureus

Insulinoma is a rare neuroendocrine tumor. It may occur sporadically or as part of the genetic tumor syndrome multiple endocrine neoplasia type 1 (MEN1). Diagnosis is challenging because of the small size of insulin producing tumors that lead to hype

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee551756e05813f7a8516629cea60035
http://europepmc.org/articles/PMC7305576

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Oncogenic osteomalacia secondary to glomus tumor

Autor: Majid Assadi, Mitra Dashtizadeh, Katayoun Vahdat, Iraj Nabipour, Kamyar Asadipooya, Mohammad Hossein Dabbaghmanesh, Basir Hashemi, Samaneh Hasanzadeh, Mohammadreza Kalantarhormozi, Mohammdreza Ravanbod, Rishi Raj

Publikováno v: Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2021)
Endocrinology, Diabetes & Metabolism Case Reports

Summary Oncogenic osteomalacia secondary to glomus tumor is extremely rare. Localization of causative tumors is critical as surgical resection can lead to a complete biochemical and clinical cure. We present a case of oncogenic osteomalacia treated w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff7c27f89c788b74650736cb1d269fdc
https://doi.org/10.1530/edm-20-0202

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Jaffe–Campanacci syndrome: Any role for 99mTc-methylene diphosphonate bone and 99mTc-octreotide scans for evaluation of the disorder?

Autor: Mohsen Qutbi, Sajad Ghanbari, Babak Shafiei, Isa Neshandar Asli

Publikováno v: World Journal of Nuclear Medicine
World Journal of Nuclear Medicine, Vol 18, Iss 2, Pp 189-191 (2019)

Jaffe–Campanacci syndrome (JCS) is a rare clinical disorder with almost unknown etiology. The main feature of this syndrome is skeletal involvement as nonossifying fibroma which may cause severe morbidity to these patients. X-ray imaging is the wid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcbf4935d3ba823ea05227d8ad80d22b
https://doi.org/10.4103/wjnm.wjnm_21_18

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Diagnostic accuracy of technetium-99m-octreotide in imaging neuroendocrine tumors, Oman hospital experience with literature review

Autor: Aymen Al Hadidi, Badriya Al Suqri, Naima Al Bulushi, Marwa Al Aamri, Mimouna Al Risi, Mohammed Al Zadjali, Hafidh Al Jahdami

Publikováno v: World Journal of Nuclear Medicine, Vol 18, Iss 2, Pp 137-142 (2019)
World Journal of Nuclear Medicine

The aim of this observational cross-sectional study with retrospective review of the data is to evaluate the efficacy of using technetium-99m-octreotide (Tc-99m-OCT) in imaging neuroendocrine tumors (NETs) in our tertiary care hospital. A total of 58

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd4a2e30ca9ef89fba2c42c2c1598696
http://www.wjnm.org/article.asp?issn=1450-1147

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