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Gotowe bibliografie tematyczne / Pituitary Micro Adenoma

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Gotowa bibliografia na temat „Pituitary Micro Adenoma”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Pituitary Micro Adenoma"

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Rambharat, Bairwa, and S. Rai G. "A Case of Atypical Pituitary Macro Adenoma." PJSR 14, no. 1 (2020): 1–7. https://doi.org/10.5281/zenodo.8228278.

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We report a case of 17 years old male with chief complaints of severe right hemi cranial headache since 3 days for  which he seeks advice from local doctor, but did not get relief. Patient also has short height and markedly decreased vision  since last 6 weeks. Patient under gone for MRI brain with contrast revealed a large “figure of 8” markedly enhancing sellar  mass with suprasellar and right para sellar extension s/o atypical pituitary macro adenoma. Markedly raised Serum prolactin  (470ng/ml) and mildly reduced FSH & LH were noted.

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Takano, Shingo, Hiroyoshi Akutsu, Takuma Hara, Tetsuya Yamamoto, and Akira Matsumura. "Correlations of Vascular Architecture and Angiogenesis with Pituitary Adenoma Histotype." International Journal of Endocrinology 2014 (2014): 1–12. http://dx.doi.org/10.1155/2014/989574.

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Vascular endothelial growth factor (VEGF) is a potent angiogenic factor in solid tumors. However, its role in angiogenesis in pituitary adenoma is controversial. Angiogenesis in solid tumors including pituitary adenoma is commonly evaluated by microvascular density (MVD). Here, we evaluated MVD and the role of VEGF in vascular architecture in 51 pituitary adenomas (24 nonfunctioning, 13 prolactin-secreting, 10 growth hormone-secreting, 3 adrenocorticotropic hormone-secreting, and 1 thyroid-stimulating hormone-secreting). Paraffin sections were stained with CD34 and VEGF. MVD and vascular archi

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Shyukyurov, S. D., and V. A. Mirzazade. "DETERMINATION OF THE ODDS RATIO FOR DETECTION OF MICRO- AND MACROPROLACTINOMA DEPENDING ON THE LEVEL OF HYPERPROLACTINAEMIA." "The Medicine and Science" scientific-practical journal named after A.Aliyev 2, no. 36 (2024): 89–93. https://doi.org/10.61775/2413-3302.v2i36.13.

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This study examines the determination of the odds ratio of detecting micro- and macroprolactinomas according to the level of hyperprolactinaemia. Purpose. To determine the odds ratio for detection of microprolactinoma and macroprolactinoma depending on the level of hyperprolactinaemia. Material and methods. 139 patients were included in the study and divided into 2 groups: group 1-hyperprolactinaemia without pituitary adenoma (n=26) and group 2-hyperprolactinaemia with pituitary adenoma (n=113). Of 113 patients in group 2, 60 had microadenoma and 53 had macroadenoma. Results. The results show

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Nair, Aiswarya K., Haritha Sagili, Jayalakshmi Dorairaj, and T. Parvathi. "Acromegaly incidentally diagnosed at term in a pregnant woman presenting with ventricular premature complexes." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 10, no. 7 (2021): 2907. http://dx.doi.org/10.18203/2320-1770.ijrcog20212693.

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Pituitary adenomas lead to increased growth hormone production and acromegaly. Pregnancy in acromegaly is rare as spontaneous conception is affected. We presented a case of 31 year old lady conceived by ovulation induction and presented at term gestation with ventricular premature complexes and was subsequently diagnosed with pituitary micro adenoma causing acromegaly. There has been no reported case of pregnancy with acromegaly presenting with premature ventricular complexes. Moreover, diagnosis of acromegaly in pregnancy is difficult and limited literature is available on its effects as well

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International, Journal of Medical Science and Innovative Research (IJMSIR). "Multiple Endocrine Neoplasia Type 1: A Case Report." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 6 (2024): 131–38. https://doi.org/10.5281/zenodo.15449118.

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<strong>Abstract</strong> <strong>Background: </strong>Multiple endocrine neoplasia type 1 (MEN1) is a rare genetic syndrome inherited in an autosomal dominant pattern, resulting from mutations in the MEN1 tumor suppressor gene. Diagnosis is typically established based on clinical criteria, characterized by the presence of two or more primary MEN1-associated tumors (including parathyroid, anterior pituitary, and pancreatic islet tumors). Here, we present the case of a patient who exhibited classic clinical features and imaging findings consistent with MEN1. <strong>Case Report: </strong>A man

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Rajani, Mehak, Yumna Mirza, Rohan Advani, Syed Muhammad Adnan Ali, and Syed Ather Enam. "Role of microRNAs in non-functioning pituitary adenoma." Journal of the Pakistan Medical Association 72, no. 01 (2022): 126. http://dx.doi.org/10.47391/jpma.3149.

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Non-functioning pituitary adenomas account for 30% of anterior pituitary tumours. Based on their inability to secrete hormones, these are often diagnosed incidentally or due to pressure symptoms. Understanding the pathogenesis of these adenomas can provide insight into factors leading to its progression and serving as biomarkers for early recognition. A literature search was performed in the current narrative review for articles published in PubMed for the last 10 years till January 2020 on micro-ribonucleic acid involved in the pathogenesis of non-functioning pituitary adenomas. Of the 478 ar

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Krzentowska, Anna, and Maria Smoter. "Clinical and Radiological Characteristics of a Patient with a Pituitary Tumor of the Prolactinoma Type — Case Report." Journal of Neurological and Neurosurgical Nursing 13, no. 2 (2024): 78–84. http://dx.doi.org/10.15225/pnn.2024.13.2.5.

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Introduction. Prolactinoma is a benign tumor of the anterior lobe of the pituitary gland. It is the most common type of pituitary adenoma. In terms of size, micro- and macroprolactinomas are distinguished. Prolactinoma is mostly a benign tumor (>98%). Symptoms in hyperprolactinemia are the result of excess hormone and mass effect. Symptoms of the mass effect include headaches, visual disturbances and dizziness. Excess prolactin leads to infertility and “amenorrhea — galactorrhea” syndrome. Aim. To increase general understanding and awareness of the symptoms, causes, and treatments of patien

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Suyambulingam, Anbalagan. "A Headache - Free Journey: Managing Pituitary Micro - Adenoma in a Young Unmarried Woman." International Journal of Science and Research (IJSR) 13, no. 5 (2024): 1459. http://dx.doi.org/10.21275/sr24523165233.

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Aryal, Saroj Babu, Shasank Chitrakar, and Akriti Panthi. "Conjunction of ovarian dermoid cyst in a patient with Pituitary Micro Adenoma: A Case Report." Journal of Nepal Medical Association 63, no. 287 (2025): 533–36. https://doi.org/10.31729/jnma.9122.

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Pituitary adenomas are common intracranial tumors, and ovarian dermoids are frequently encountered benign gynecological lesions. While both conditions are individually prevalent, their co-existence is rare and infrequently reported. This unusual combination may pose diagnostic challenges and warrants further exploration to determine any potential underlying link. We present a case of a 42-year-old Hindu female who was diagnosed case of a pituitary adenoma with a leftsided ovarian dermoid cyst resulting in a gynecological and hormonal imbalance. The diagnosis was confirmed by subsequent related

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Gedvilaite-Vaicechauskiene, Greta, Loresa Kriauciuniene, Arimantas Tamasauskas, et al. "Pituitary Adenoma: SSTR2 rs2236750, SSTR5 rs34037914, and AIP rs267606574 Genetic Variants, Serum Levels, and Ki-67 Labeling Index Associations." Medicina 60, no. 8 (2024): 1252. http://dx.doi.org/10.3390/medicina60081252.

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Background and Objectives: This study explores the complex pathogenesis of pituitary adenomas (PAs), prevalent intracranial tumors in the pituitary gland. Despite their generally benign nature, PAs exhibit a diverse clinical spectrum involving hormone hypersecretion and varying invasiveness, hinting at multifaceted molecular mechanisms and abnormalities in tumorigenesis and gene regulation. Materials and Methods: The investigation focuses on the Ki-67 labeling index, SSTR2 rs2236750, SSTR5 rs34037914, and AIP rs267606574 polymorphisms, alongside serum levels of SSTR2, SSTR5, and AIP, to discer

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Streszczenia konferencji na temat "Pituitary Micro Adenoma"

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Gummadavelli, Abhijeet, Lily McCarthy, Zeynep Erson, Eugenia Vining, Murat Gunel, and S. Bulent Omay. "Micro-RNA Mutations Across Multiple Resections of a Giant Nonfunctional Pituitary Adenoma." In 30th Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1702680.

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