Literature DB >> 17003015

Pituitary hyperplasia.

Mubarak Al-Gahtany1, Eva Horvath, Kalman Kovacs.   

Abstract

Pituitary hyperplasia is rare, difficult to diagnose and sometimes controversial. The hyperplasia could be physiologic which is usually reversible, or pathologic which varies in presentation from incidental to tumor like lesion with and without hormonal disturbance. Any pituitary cell is capable of undergoing hyperplasia in the presence of the right stimuli. In this article we summarize the various pathologic and morphologic features of each subtype of pituitary hyperplasia, give an account of the molecular, hormonal and cellular basis of this condition and outline its clinical significance, differential diagnosis and prognosis.

Entities:  

Year:  2003        PMID: 17003015     DOI: 10.14310/horm.2002.1195

Source DB:  PubMed          Journal:  Hormones (Athens)        ISSN: 1109-3099            Impact factor:   2.885


  14 in total

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Authors:  Shlomo Melmed
Journal:  Nat Rev Endocrinol       Date:  2011-03-22       Impact factor: 43.330

Review 2.  Advances and controversies in the classification and grading of pituitary tumors.

Authors:  E R Laws; D L Penn; C S Repetti
Journal:  J Endocrinol Invest       Date:  2018-06-01       Impact factor: 4.256

3.  Waxing and waning of a pituitary mass in a young woman with combined pituitary hormone deficiency (CPHD) due to a PROP-1 mutation.

Authors:  Sergio Oliva Nascif; Teresa Cristina Vieira; João Carlos Ramos-Dias; Ana-Maria Judith Lengyel; Julio Abucham
Journal:  Pituitary       Date:  2006       Impact factor: 4.107

4.  Primary intracranial neuroendocrine tumor with ectopic adrenocorticotropic hormone syndrome: A rare and complicated case report and literature review.

Authors:  Hailong Liu; Mingshan Zhang; Xuan Wang; Yanming Qu; Hongwei Zhang; Chunjiang Yu
Journal:  Mol Clin Oncol       Date:  2016-05-11

5.  Characterization of GPR101 transcript structure and expression patterns.

Authors:  Giampaolo Trivellin; Ivana Bjelobaba; Adrian F Daly; Darwin O Larco; Leonor Palmeira; Fabio R Faucz; Albert Thiry; Letícia F Leal; Liliya Rostomyan; Martha Quezado; Marie Helene Schernthaner-Reiter; Marija M Janjic; Chiara Villa; T John Wu; Stanko S Stojilkovic; Albert Beckers; Benjamin Feldman; Constantine A Stratakis
Journal:  J Mol Endocrinol       Date:  2016-06-09       Impact factor: 5.098

6.  Pituitary hyperplasia: case series and literature review of an under-recognised and heterogeneous condition.

Authors:  Sunita M C De Sousa; Peter Earls; Ann I McCormack
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2015-06-01

7.  Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study.

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Journal:  Acta Neuropathol Commun       Date:  2016-06-01       Impact factor: 7.801

8.  Comparative Analysis of Clinical, Hormonal and Morphological Studies in Patients with Neuroendocrine ACTH-Producing Tumours.

Authors:  G S Kolesnikova; A M Lapshina; I A Voronkova; E I Marova; S D Arapova; N P Goncharov; I I Dedov
Journal:  Int J Endocrinol       Date:  2013-02-19       Impact factor: 3.257

9.  Primary intracranial neuroendocrine tumor: two case reports.

Authors:  Hailong Liu; Haoran Wang; Xueling Qi; Chunjiang Yu
Journal:  World J Surg Oncol       Date:  2016-04-30       Impact factor: 2.754

10.  The prevalence of brain abnormalities in boys with central precocious puberty may be overestimated.

Authors:  Jong Seo Yoon; Cheol Hwan So; Hae Sang Lee; Jung Sub Lim; Jin Soon Hwang
Journal:  PLoS One       Date:  2018-04-03       Impact factor: 3.240

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