Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Endocrine Neoplasia Case Reports II"'
Autor:
Kaushal Vinaykumar Sheth, Aashish Reddy, Ravindra Vottery, Chimutai Chinte, Vidya Tickoo, Raman Boddula, Ashok Venkatanarasu, Santosh Basavaraju
Publikováno v:
Journal of the Endocrine Society
INTRODUCTION Ectopic ACTH constitutes 5-10% of ACTH dependent Cushing’s syndrome. Evolution of symptoms can be rapid. Cortisol & ACTH is usually higher as compared to Cushing’s disease. Imaging studies should be obtained for localization of the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c612ef9a4cfe9ced3a75db7f75a43b40
http://europepmc.org/articles/PMC7208775
http://europepmc.org/articles/PMC7208775
Autor:
Parinya Samakkarnthai, Manaporn Payanundana, Chonpiti Siriwan, Siroj Dejhansathit, Kenneth Nugent, Ana Marcella Rivas Mejia, Nattapol Sathavarodom, Subhanudh Thavaraputta
Publikováno v:
Journal of the Endocrine Society
Background: Glucagonomas are pancreatic tumors arising from the islets cell of Langerhans that over secrete glucagon. Necrolytic migratory erythema (NME) is an important feature for the recognition of glucagonomas. Glucagonomas occurring in MEN1 is i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9dc3f986b20a9fbcfbab87fdae1ec24
http://europepmc.org/articles/PMC7208985
http://europepmc.org/articles/PMC7208985
Publikováno v:
Journal of the Endocrine Society
Primary Amenorrhea, Growth Arrest and Metabolic Syndrome Due to an Unclassfied Hepatocellalar Adenoma. Background: Hepatocellular adenoma is a rare benign neoplasm, seldom ascribed as the cause of endocrine and metabolic derrangement. We herein repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1f6f7eb860160b9eb7cd1595397bc11
http://europepmc.org/articles/PMC7207348
http://europepmc.org/articles/PMC7207348
Autor:
Nadeem M Rais, Sandeep Kumar Mathur, Savinitha Prakash, Anshul Kumar, Apoorva Joshi, Vinod Scaria, Swetha Jain
Publikováno v:
Journal of the Endocrine Society
Introduction The MEN 1 syndrome is an enigmatic disorder, manifesting a wide spectrum of disorders, in members of a family, harbouring the same gene mutation. We present one such family, with a MENIN gene mutation with marked diversity in the clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7d6240ee15fcfbac03ae795082d53b0
http://europepmc.org/articles/PMC7208113
http://europepmc.org/articles/PMC7208113
Publikováno v:
Journal of the Endocrine Society
Tumors of chromaffin cells derived from the embryonic neural crest are classified as pheochromocytomas when located in the medulla of the adrenal glands and paragangliomas when located externally to it. Bladder paragangliomas constitute less than 1%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::257b5f9020741ca652f513852525061f
http://europepmc.org/articles/PMC7209111
http://europepmc.org/articles/PMC7209111
Autor:
Yotam Weiner, Omar Jameel
Publikováno v:
Journal of the Endocrine Society
Background: Pheochromocytomas are neuroendocrine tumors that release large amounts of metanephrines and catecholamines, resulting in a wide array of symptoms including hypertension, diaphoresis, and headaches. If left unrecognized they can lead to se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116ac0e6d8157e505a01ebab7c54ce27
http://europepmc.org/articles/PMC7208666
http://europepmc.org/articles/PMC7208666
Autor:
Samantha Anandappa, Louise Izatt, Dimitra Christodoulou, Louise Breen, Mamta Joshi, Anand Velusamy, Audrey Jacques, Paul V. Carroll, Barbara McGowan, Ramesh Thurairaja
Publikováno v:
Journal of the Endocrine Society
Introduction: Bladder Paragangliomas (PGLs) are rare neuroendocrine tumors derived from sympathetic paraganglionic tissue within the bladder wall, accounting for 40% of PPGLs are associated with inherited syndromes through mutations affecting citric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::197fef2673918916dd15613d50f7092d
http://europepmc.org/articles/PMC7209050
http://europepmc.org/articles/PMC7209050
Autor:
Gustavo R Armaiz-Pena, Joy Wortham, Lyan Gondin Hernandez, Maureen Koops, Jan M. Bruder, Brenda Sandoval, Carolina Solis-Herrera, Jonathan Trejo, Ramona Granda-Rodriguez
Publikováno v:
Journal of the Endocrine Society
Parathyroid carcinomas have an estimated prevalence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b47e68452faf9bb3d32d397b5581e37
http://europepmc.org/articles/PMC7207705
http://europepmc.org/articles/PMC7207705
Publikováno v:
Journal of the Endocrine Society
Background: Ovarian testosterone producing tumors are an uncommon cause of hirsutism, pulmonary embolus and polycythemia. Clinical Case: A 67-year-old Caucasian postmenopausal woman was referred for Endocrine evaluation of a one-year history of hirsu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65fd4531506240c58f4dcbeacb99e979
http://europepmc.org/articles/PMC7207338
http://europepmc.org/articles/PMC7207338
Autor:
Katrina Conard, Tina Y Hu, Loren Berman, Tejal Mody, Anthony Gannon, Jeanne M. Franzone, William J. Parkes
Publikováno v:
Journal of the Endocrine Society
BACKGROUND: Parathyroid carcinoma (PC) is exceptionally rare in children and its clinical features are poorly understood. Available reports have identified that very high serum calcium and parathyroid hormone levels would be expected in this disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::430feb3a1280e0970f22573851d635b9
http://europepmc.org/articles/PMC7208292
http://europepmc.org/articles/PMC7208292