Background and objective Management of recurrent acromegaly is challenging for both
neurosurgeons and endocrinologists. Several treatment options including repeat surgery …

Acromegaly-related sub/infertility, tidily related to suboptimal disease control (1/2 of cases),
correlates with hyperprolactinemia (1/3 of patients), hypogonadotropic hypogonadism …

Aims Aim of the present analysis was to report results of a systematic review of the literature
in the setting of patients treated with hypoF PT for benign lesions of the central nervous …

The review discusses the relationship between acromegaly and uterine fibroids. It highlights
variations in research methodologies and inconsistent findings, emphasizing the complex …

Purpose In patients with acromegaly, secondary treatment options in cases of hormonal non-
remission or tumor progression include repeat transsphenoidal surgery (TSS), radiation …

Acromegaly is a rare endocrine syndrome characterized by unrestrained growth hormone
(GH) secretion from a GH-secreting pituitary neuroendocrine tumor (PitNET). Data on sleep …

Acromegaly is characterised by the hypersecretion of growth hormone and poses diagnostic
and therapeutic challenges requiring consensus and guidelines for effective management …

The goal of this study was to measure arginase enzyme activity in diabetic acromegaly Iraqi
patients and compare it to a control group. This study included 80 participants, whose ages …

All pituitary adenomas, with the probable exception of prolactinoma, must initially undergo
surgery. As a result, choosing the best surgical strategy and ensuring the safest possible …

Objetivo: Analisar as características da Acromegalia. Revisão Bibliográfica: A acromegalia é
uma doença endócrina rara associada a níveis elevados de hormônio do crescimento e …