Preoperative medical treatment for patients with acromegaly: yes or no?

F Albarel, T Cuny, T Graillon, H Dufour… - Journal of the …, 2022 - academic.oup.com
Transsphenoidal surgery is the first-line treatment for acromegaly. However, several factors
can modify surgical remission rates, such as the initial hormone levels, the size and …

Ki67 in endocrine neoplasms: to count or not to count, this is the question! A systematic review from the English language literature

E Guadagno, E D'Avella, P Cappabianca… - Journal of …, 2020 - Springer
Background Endocrine neoplasms are generally slow-growing tumors that can show
hormonal activity and give metastases. In most cases they are benign and clearly malignant …

Real-life clinical impact of a five-tiered classification of pituitary tumors

N Sahakian, R Appay, N Resseguier… - European journal of …, 2022 - academic.oup.com
Introduction Usually benign, pituitary tumors (PT) can be invasive and aggressive with a
propensity to progress and/or recur. Trouillas's clinicopathological classification attempts to …

A nomogram for preoperatively predicting the Ki-67 index of a pituitary tumor: A retrospective cohort study

X Cai, J Zhu, J Yang, C Tang, F Yuan, Z Cong… - Frontiers in …, 2021 - frontiersin.org
Background The Ki-67 index is an indicator of proliferation and aggressive behavior in
pituitary adenomas (PAs). This study aims to develop and validate a predictive nomogram …

[HTML][HTML] Immunohistochemical evaluation of biomarkers with predictive role in acromegaly: a literature review

MC Gliga, LG Tătăranu, M Popescu… - Romanian Journal of …, 2023 - ncbi.nlm.nih.gov
Acromegaly is a rare endocrine disorder, which despite the recent advances in diagnosis
and management, remains a significant burden in terms of morbidity and mortality for …

Recurrent cushing's disease in adults: predictors and long-term follow-up

M Ünal, A Selek, M Sözen, E Gezer… - Hormone and …, 2023 - thieme-connect.com
Cushing's disease (CD) is characterized by endogenous hypercortisolism that is associated
with increased mortality and morbidity. Due to high recurrence rates in CD, the …

Medication for acromegaly reduces expression of MUC16, MACC1 and GRHL2 in pituitary neuroendocrine tumour tissue

R Saksis, I Silamikelis, P Laksa, K Megnis… - Frontiers in …, 2021 - frontiersin.org
Acromegaly is a disease mainly caused by pituitary neuroendocrine tumor (PitNET)
overproducing growth hormone. First-line medication for this condition is the use of …

MGMT immunohistochemistry in pituitary tumors: controversies with clinical implications

G Kontogeorgos, E Thodou, M Koutourousiou… - Pituitary, 2019 - Springer
Introduction Temozolomide (TMZ) is currently considered as a rational therapeutic option for
patients with progressively aggressive pituitary adenomas and carcinomas not responding …

SNPs of miR-23b, miR-107 and HMGA2 and their Relations with the Response to Medical Treatment in Acromegaly Patients

DM Armagan, AS Akdemir, HM Ozkaya… - Experimental and …, 2021 - thieme-connect.com
Introduction Acromegaly is a chronic disease of increased growth hormone (GH) secretion
and elevated insulin-like growth factor-I (IGF-I) levels induced by a pituitary adenoma …

[HTML][HTML] Using a Precision Approach to Optimize the Drug Therapy of Patients With Acromegaly Syndrome

VS Pronin, MB Antsiferov, TM Alekseeva… - The Pituitary Gland-An …, 2023 - intechopen.com
Modern problems of acromegaly treatment are associated with the heterogeneous
composition of somatotrophic tumors, differing in clinical course and sensitivity to the …