Results 101 to 110 of about 158,592 (235)
Tumor Biology, 2017 Human pituitary adenoma is one of the most common intracranial tumors with an incidence as high as 16.7%. Recent evidence has hinted a relationship between growth factors of pituitary or hypothalamic origin and proliferation of human pituitary adenoma ...
Kai Zhou +6 more
doaj +1 more source
Evolutionary Signal and Development of the Foramen Dorsum Sellae (Nov.) Across Primates
Journal of Morphology, Volume 287, Issue 9, September 2026.The dorsum sellae of the sphenoid bone occasionally exhibits an accessory opening, though its significance is unknown. We scored its presence in humans (N = 114) and 30 non‐human primate genera (N = 1468) and combined histological, dissection‐based, and phylogenetic approaches to understand its function. The foramen occurred in 12% of humans and 33% of
Stephanie L. Canington +7 more
wiley +1 more source
Collision Tumor in the Pituitary, Concurrent Pituitary Adenoma, and Craniopharyngioma
, 2020 Collision tumors are two independent, distinct tumors occupying the same anatomical space. This case presents a pituitary adenoma-craniopharyngioma collision tumor presenting with hemianopsia. A 60-year-old with a past history of a nonsecretory pituitary
Zaid Shareef +4 more
core +1 more source
Synchronous pituitary adenoma and pituicytoma
, 2016 Pituicytoma is a rare benign neoplasm arising in the sellar region, usually found in the posterior lobe and/or pituitary stalk. Here, we report the case of a 67-year-old woman who presented with bitemporal hemianopsia and visual impairment accompanied by
Regli, Luca +7 more
core +1 more source
POSTOPERATIVE VASOSPASM IN PITUITARY ADENOMA WITH PITUITARY APOPLEXY [PDF]
, 1994 A patient who developed complications relating to intracranial arterial vasospasm following transcranial removal of a pituitary adenoma with pituitary apoplexy is reported. A 23-year-old female was admitted because of headache.
Nakase, Hiroyuki +5 more
core +1 more source
Acromegaly with no pituitary adenoma and no evidence of ectopic source
Indian Journal of Endocrinology and Metabolism, 2011 More than 99% of patients with acromegaly harbor a growth hormone (GH) secreting pituitary adenoma. As the time from onset of signs/symptoms to diagnosis of acromegaly is long (symptom onset to diagnosis is often 4-10 years), pituitary adenomas that ...
Deepak Khandelwal +3 more
doaj +1 more source
Movement Disorders Clinical Practice, Volume 13, Issue 9, Page 2250-2258, September 2026.Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Sangeetha Yoganathan +14 more
wiley +1 more source
Psychiatry and Clinical Neurosciences Reports, Volume 5, Issue 3, September 2026.Abstract Aim This study aimed to compare social participation and physical activity in patients with craniopharyngioma or central nervous system germ cell tumor (CNS germ cell tumor) with those of healthy participants and examine their associations with social behavioral disorders.
Misa Komaki +10 more
wiley +1 more source
Acromegaly without Imaging Evidence of Pituitary Adenoma
, 2010 Context: GH-secreting pituitary adenomas are nearly always visible on conventional magnetic resonance (MR) imaging. However, management and outcome of acromegalic patients lacking imaging evidence of GH-secreting pituitary adenomas are undefined.
Russell R. Lonser +4 more
core +1 more source
Sellar collision tumor involving pituitary gonadotroph adenoma and chondroma: a potential clinical diagnosis [PDF]
, 2011 We report on a 74-year-old male patient who presented with progressive neuroophthalmologic symptoms soon after the administration of a long-acting gonadotropin-releasing hormone agonist for treatment of a prostate cancer. Imaging revealed a destructively
Christ, Emanuel +4 more
core +2 more sources