نتایج جستجو برای: congenital hypopituitarism

تعداد نتایج: 121663  

Journal: :Clinical endocrinology 2010
Trevor A Howlett Miles J Levy Iain J Robertson

Autoimmune hypophysitis is a rare chronic inflammatory condition of the pituitary gland which typically presents with hypopituitarism and a pituitary mass. Cases involving anterior pituitary alone (65%) are six times more common in women, typically presenting during pregnancy or postpartum (57%). Anterior and posterior pituitary involvement (25%) are twice as common in women, and neurohypophysi...

2010
Zouhour Fadoukhair Mounia Amzerin Nabil Ismaili Rhizlane Belbaraka Rachida Latib Yassir Sbitti Hind M'rabti Saber Boutayeb Mohammed Ichou Hassan Errihani

BACKGROUND The most common cause of hypopituitarism is pituitary adenoma. However, in the case of suprasellar masses different etiologies are possible. We report an unusual case of primary suprasellar lymphoma presented with hypopituitarism. CASE PRESENTATION A 26 year old woman presented with amenorrhea, galactorrhea and neurological disorders. Also, the laboratory work-up revealed partial h...

2016
Marlene Tarvainen Satu Mäkelä Jukka Mustonen Pia Jaatinen

Puumala hantavirus (PUUV) infection causes nephropathia epidemica (NE), a relatively mild form of haemorrhagic fever with renal syndrome (HFRS). Hypophyseal haemorrhage and hypopituitarism have been described in case reports on patients with acute NE. Chronic hypopituitarism diagnosed months or years after the acute illness has also been reported, without any signs of a haemorrhagic aetiology. ...

2018
Khuram Khan Saqib Saeed Alexius Ramcharan Sanjiv Gray

INTRODUCTION Traumatic brain injury (TBI) is one of the main causes of morbidity and mortality in young trauma patients with resultant multi-organ effects. Hypopituitarism following TBI can be debilitating and life threatening. TBI which causes hypopituitarism may be characterized by a single head injury, such as from a motor vehicle accident, or by chronic repetitive head trauma, as seen in co...

2011
Manohara Kenchaiah Steve L Hyer

INTRODUCTION Diffuse large B-cell non Hodgkin's lymphoma may involve the pituitary either as a primary central nervous system lymphoma or, more frequently, as metastasis from systemic lymphoma leading to hypopituitarism. A partial recovery of pituitary function after treatment with chemotherapy has previously been described but complete recovery with cessation of all hormone supplements is exce...

2015
Gulden Diniz Ozgur Olukman Sebnem Calkavur Muammer Buyukinan Canan Altay

Malignant infantile osteopetrosis is a rarely seen severe disorder which appears early in life with general sclerosis of the skeleton. It is caused by functionally defective osteoclasts which fail to resorb bone. Affected infants can exhibit a wide spectrum of clinical manifestations including impaired hematopoiesis, hepatosplenomegaly, visual impairment, and hypocalcemia. With the exception of...

Journal: :Endocrine journal 2004
Seong Jin Lee Hyung Joon Yoo Sung Woo Park Moon Gi Choi

Lymphocytic hypophysitis is a rare inflammatory disease of the pituitary gland that is being increasingly recognized as a cause of hypopituitarism. This condition may be due to an autoimmune pituitary destruction which usually occurs in young women during pregnancy or in the immediate postpartum period. We describe a case of cystic pituitary mass in a thirty-eight year-old woman presenting with...

2017
Shousen Wang Biao Li Chenyu Ding Deyong Xiao Liangfeng Wei

The purpose of this study was to investigate the differences between pre- and postoperative pituitary hormone levels in patients undergoing surgical resection of pituitary adenoma and to identify factors associated with preoperative hypopituitarism. Data from 81 patients with histologically confirmed functioning and non-functioning pituitary adenomas (NFPA) who underwent transsphenoidal resecti...

Journal: :International Journal of Advances in Medicine 2021

Sheehan's syndrome is a form of hypopituitarism caused by pituitary gland necrosis hemorrhagic shock during pregnancy. It's rare issue with wide range symptoms and long time to diagnose. A 40-year-old female presented giddiness which was rotatory type followed headache, vomiting associated nausea, decreased appetite for one week. She has experienced excessive vaginal bleeding secondary amenorrh...

2017
Katie Daughters Antony S R Manstead D Aled Rees

PURPOSE Central diabetes insipidus is characterised by arginine vasopressin deficiency. Oxytocin is structurally related to vasopressin and is synthesised in the same hypothalamic nuclei, thus we hypothesised that patients with acquired central diabetes insipidus and anterior hypopituitarism would display an oxytocin deficiency. Moreover, psychological research has demonstrated that oxytocin in...

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