نتایج جستجو برای: pituitary macroadenoma

تعداد نتایج: 44529  

ژورنال: Basic and Clinical Neuroscience 2016
Goldschlager, Tony, Hall, Jonathan, Lim, Kai-Zheong, Pullar, Michael, Uren, Brent, V. Chandra, Ronil,

Introduction: The co-existence of pituitary adenoma and meningioma is extremely rare. It is even rarer in patients with no previous known risk factors for either tumour. Here, we present a case of synchronous non-functioning pituitary adenoma with suprasellar and olfactory groove meningiomas in a patient without previous irradiation. Methods: The tumours were diagnosed on MRI in the 65-year-ol...

Journal: :AJNR. American journal of neuroradiology 2006
A M Tokumaru I Sakata H Terada S Kosuda H Nawashiro M Yoshii

PURPOSE Visual acuity (VA) disturbance other than field defect is important in evaluating patients with pituitary macroadenoma. The purpose of this study was to evaluate MR imaging appearances of optic nerves in patients with pituitary macroadenoma and to ascertain whether visual impairment was correlated with abnormality in optic nerve signal intensity. PATIENTS AND METHODS Twenty-seven pati...

2013
S. Wacharasindhu S. Shuangshoti S. Sunthornyothin

Patients with long-standing hypothyroid are, in some cases, reported to develop pituitary gland hyperplasia due to loss of feedback inhibition of thyroxine in hypothalamus-the condition of which typically regresses after thyroxine replacement. Herein, a 15-year-old girl-with long-standing untreated lingual hypothyroid-presents with a pathologically proven TSH pituitary macroadenoma and bilatera...

2012
D Campbell NK Amponsah R Mott T Ellis

The authors present the case of a 58-year-old gentleman presenting with atypical carcinoid tumor of primary lung origin metastasizing to a previously identified pituitary macroadenoma. The patient presented with symptoms of headache and visual disturbance. Imaging revealed enlargement of a known sellar mass as well as three separate enhancing lesions in the brain parenchyma. Resection was accom...

2014
Juan Jakez-Ocampo Yemil Atisha-Fregoso Luis Llorente

Hyperprolactinemia has been related to autoimmune diseases. Herein, we describe a case of a female with a prolactin producer pituitary macroadenoma who developed severe polymyositis one month after its removal. The patient had very high levels of CPK and muscle biopsy showed remarkable inflammatory infiltration. Steroid therapy was followed with total recovery. To the best of our knowledge, thi...

2012
Morteza Sanei Taheri Ramin Pourghorban Massoud Sajadi Nassab Reza Pourghorban

Intraosseous lipoma is a rare benign tumor, mostly occurring in lower limb especially in os calcis and the metaphyses of long bones. Intraosseous lipoma of the skull is even rarer, with 12 cases having been reported to involve the sphenoid bone in the literature. We present the third reported case of sphenoclival intraosseous lipoma in a 43-year-old man with headache, hyperprolactinemia and vis...

2016
Kai-Zheong Lim Tony Goldschlager Ronil V. Chandra Jonathan Hall Brent Uren Michael Pullar

INTRODUCTION The co-existence of pituitary adenoma and meningioma is extremely rare. It is even rarer in patients with no previous known risk factors for either tumour. Here, we present a case of synchronous non-functioning pituitary adenoma with suprasellar and olfactory groove meningiomas in a patient without previous irradiation. METHODS The tumours were diagnosed on MRI in the 65-year-old...

2016
Fergus Keane Aoife M Egan Patrick Navin Francesca Brett Michael C Dennedy

UNLABELLED Pituitary apoplexy represents an uncommon endocrine emergency with potentially life-threatening consequences. Drug-induced pituitary apoplexy is a rare but important consideration when evaluating patients with this presentation. We describe an unusual case of a patient with a known pituitary macroadenoma presenting with acute-onset third nerve palsy and headache secondary to tumour e...

2017
Gulay Simsek Bagir Soner Civi Ozgur Kardes Fazilet Kayaselcuk Melek Eda Ertorer

Pituitary apoplexy (PA) may very rarely present with hiccups. A 32-year-old man with classical acromegaloid features was admitted with headache, nausea, vomiting and stubborn hiccups. Pituitary magnetic resonance imaging (MRI) demonstrated apoplexy of a macroadenoma with suprasellar extension abutting the optic chiasm. Plasma growth hormone (GH) levels exhibited suppression (below <1 ng/mL) at ...

Journal: :Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2002
Anita Skandarajah Wai Hoe Ng Michael Gonzales Andrew H Kaye

Lymphocytic hypophysitis is an uncommon disease with a variable presentation and unclear pathophysiology. We present the case of a 30 year old woman who presented with features typical of a pituitary macroadenoma. She underwent a transphenoidal resection of the mass and histopathological examination revealed lymphocytic hypophysitis. This case illustrates the difficulty in differentiating pitui...

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