Results 71 to 80 of about 218,733 (151)
Background. In modern international guidelines, there are not distinguished criteria for the evaluation of clinical symptoms, including somatic, neurological status, although almost all neuroendocrinologists acknowledge the presence exactly of ...
O.O. Khyzhniak +2 more
doaj +1 more source
The Heterogeneity of Serum hPRL in a Patient with a Giant Prolactinoma
The heterogeneity of hPRL in the serum of a patient with a giant prolactinoma (hPRL 27 micrograms/ml) was studied employing gel chromatography, RIA and lymphoma cell bioassay. After gel filtration of serum sample on Sephadex G-100 (superfine) column, a few hPRL peaks were detected by RIA.
TANAKA, Toshiaki +2 more
openaire +3 more sources
Giant prolactinoma is a rare subset of macroadenomas. Limited studies demonstrated which therapy could be successfully used in the first-line therapy of giant prolactinoma.
Turgut, Seda +5 more
core
Giant prolactinoma: case report
Objective: To report the clinical case of an adolescent with a giant prolactinoma, diagnosed at the pediatric endocrinology service of a public university hospital in Salvador, Bahia.
Ferreira, Juliane Moreira
core +1 more source
Rapid Visual Improvement After Cabergoline Therapy in a Macroprolactinoma Case
Introduction: Medical therapy with dopamin agonists (DAs) is the first treatment of choice for prolactinomas. no matter how large or how severe the neurologic sequelae and cabergoline (CAB) is the best initial choice (1).
Elif Güneş +2 more
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OBSTACLES IN MANAGING GIANT PROLACTINOMA
INTRODUCTION/BACKGROUNDSarcoidosis is a multisystem granulomatous inflammatory disorder with common involvement of the lungs, lymph nodes and heart. Neurosarcoidosis, especially hypothalamicpituitary involvement, is a rare phenomenon (<10% of sarcoidosis patients).
Siti Zakiah Ahmad Daud +4 more
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Cabergoline monotherapy in GH- and PRL-cosecreting pituitary adenomas
Functional pituitary tumours, also called pituitary neuroendocrine tumours (PitNETs), typically produce a single hormone, based on the cell lineage from which they arise in the anterior pituitary.
James M McNeil +3 more
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Case report and literature review of pituitary apoplexy in a 14-year-old girl with prolactinoma
Background Pituitary adenomas are rare in pediatric populations, with prolactinomas representing 20–39% of childhood cases. Pituitary apoplexy-hemorrhage or infarction of a pituitary adenoma-occurs in only 2–12% of tumors and is exceedingly uncommon in ...
Xuewen Yuan +3 more
doaj +1 more source

