Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Endocrine Neoplasia Case Reports III"'
Autor:
Shady Ibrahim ElEbrashy, ElRefaay Ehab
Publikováno v:
Journal of the Endocrine Society
Background: Meningioma is a rare association of Multiple endocrine neoplasia type 1 (MEN 1) and very few cases has been reported in literature. Clinical Case: a 75-year-old woman showed severe headache, disturbed consciousness and convulsions. A diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c34a986cfacde13d677d78b4448dc292
http://europepmc.org/articles/PMC7209043
http://europepmc.org/articles/PMC7209043
Publikováno v:
Journal of the Endocrine Society
Introduction: Atypical teratoid/rhabdoid tumor(ATRT) is an aggressive tumor of the central nervous system mostly seen in the pediatric age group. It is rare for these tumors to occur in adults, especially in the sellar region. Here we describe a case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1989ecde8cf097185f18f4b7ae31a9b6
http://europepmc.org/articles/PMC7207894
http://europepmc.org/articles/PMC7207894
Autor:
Francisco Javier Lopez Maldonado, Jose Fernando Montiel Castañeda, Angel Alfonso Mayorga León, Alondra Rodríguez González, Carlos Alfonso Morales Chinchillas, Jorge Leo Peterson, Jesus Alan Guardado, Itzel Denisse Ramirez Bañales, Antonio Cruz Alvarado, Eduardo Rafael Leon Milan
Publikováno v:
Journal of the Endocrine Society
Introduction Primary aldosteronism (PA) is the most common cause of secondary hypertension (HTN) that is often underdiagnosed. Patients with PA have higher cardiovascular morbidity and mortality than age- and sex- matched patients with essential HTN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e3dbfa9f8729f6851f753d47faa009e
http://europepmc.org/articles/PMC7208506
http://europepmc.org/articles/PMC7208506
Autor:
Nattapol Sathavarodom
Publikováno v:
Journal of the Endocrine Society
A 40 years old woman presented with headache, palpitation and diaphoresis by the past 3 months, and then developed progressive dyspnea on exertion and chest pain 2 weeks ago. She also lost 5 kg of her body weight during the past 6 months. She ever ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7180ac7cb02c015b0da18b03696afb4b
http://europepmc.org/articles/PMC7208382
http://europepmc.org/articles/PMC7208382
Publikováno v:
Journal of the Endocrine Society
Introduction: Beckwith-Wiedemann syndrome (BWS), a multisystem genomic imprinting disorder in chromosome 11p15.5 region, is an overgrowth syndrome often presenting with macroglossia, abdominal wall defects, hemihyperplasia, enlarged abdominal organs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bc8501b05058c91c6b9820889036591
http://europepmc.org/articles/PMC7208231
http://europepmc.org/articles/PMC7208231
Publikováno v:
Journal of the Endocrine Society
Multiple endocrine neoplasia (MEN) is characterized by the occurrence of tumors involving two or more endocrine glands in a single patient. Among the four MEN syndromes, MEN4 due to CDKN1B mutation is characterized by parathyroid and anterior pituita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a9b0c8803a8070b1e5f1d2e0b911ae9
http://europepmc.org/articles/PMC7208729
http://europepmc.org/articles/PMC7208729
Publikováno v:
Journal of the Endocrine Society
Introduction The bladder is an uncommon site for a paraganglioma, with only Clinical Case A 72-year-old man with high risk prostate cancer, Grade group 5 on biopsy, was found to have a 1.2 x 1.6 cm bladder wall mass on staging CT scan. The transmural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8df90d90e85d553f81791c88b22910b0
http://europepmc.org/articles/PMC7209377
http://europepmc.org/articles/PMC7209377
Autor:
Francisco Javier Lopez Maldonado, Angel Alfonso Mayorga León, Flor Maria Yocupicio, Karla Itzel Luareano, Eduardo Rafael Leon Milan, Alondra Rodríguez González, Carlos Alfonso Morales Chinchillas, Jesus Alan Guardado, María Elena Marín Fragoso
Publikováno v:
Journal of the Endocrine Society
Introduction Proinsulin-secreting tumors (proinsulinomas) are exceedingly rare, characterized by the predominant hypersecretion of proinsulin. We present an unusual case of hypoglycemic syndrome in a 19-year old woman with a proinsulinoma (PI). Clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8517d4036b176427f7b80c48e69fa413
http://europepmc.org/articles/PMC7208513
http://europepmc.org/articles/PMC7208513
Publikováno v:
Journal of the Endocrine Society
Adult T-cell Leukemia/lymphoma (ATL) is a rare and aggressive type of non-Hodgkin’s lymphoma. Patients with ATL commonly develop severe hypercalcemia leading to life-threatening complications like acute kidney injury, cardiac arrhythmias, altered m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::386ead0d9b17244a26f9ae8b7ec0ad5d
http://europepmc.org/articles/PMC7209624
http://europepmc.org/articles/PMC7209624
Autor:
Samia Abdullah Bokhari
Publikováno v:
Journal of the Endocrine Society
Back Ground: Epidermoid cysts (ECs) result from the inclusion of squamous epithelial elements during neural tube closure. ECs are tumors constituting 02-1.8% of all brain tumors. ECs are typically found in cerebellopontine angle, but occasionally dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32241107323446fb0522086a5f1f2d36
https://doi.org/10.1210/jendso/bvaa046.2032
https://doi.org/10.1210/jendso/bvaa046.2032