Large suprasellar aneurysms imitating pituitary tumour.

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Large suprasellar aneurysms imitating pituitary tumour.

Two patients had large (20--30 mm) suprasellar aneurysms with clinical findings resembling an expanding pituitary tumour. One aneurysm was giant (30 mm). Its delayed diagnosis for six years led to severe chiasmal compression. The other aneurysm was compressing the optic nerve. Visual improvement resulted after surgery.

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Suprasellar ectopic pituitary adenoma presenting as cranial diabetes insipidus.

We describe the occurrence of a supracellar ectopic pituitary adenoma in a 34 year old woman who presented with cranial diabetes insipidus and subsequently developed galactorrhoea-amenorrhoea. The tumour was demonstrated by both contrast computed tomography scan and magnetic resonance imaging with gadolinium enhancement and was confirmed at operation. Histological examination showed that the su...

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Mixed Germ Cell Tumour of the Suprasellar Region

Background and Importance: Intracranial germ cell tumour is a rare entity and encompasses germinomatous and non germinomatous neoplasms. These usually affect the pineal and hypothalamic regions and manifest with characteristic clinical features based on their location. A combination of mature cystic teratoma and germinoma is rare.

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Pituitary tumour pathogenesis.

Pituitary adenomas are the most common tumours in the central nervous system, make up approximately 10% of all primary intracerebral tumours [1] and are found incidentally in 3-27% of autopsies [2]. The predisposition to tumour formation of the highly specialized cellular phenotypes that characterize the anterior pituitary is unexplained, but it is tempting to speculate that the same hormones, ...

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Pituitary adenoma coexisting with a suprasellar arachnoid cyst.

OBJECTIVE Biochemical and radiological properties of sellar and parasellar lesions are quite similar in some instances. This leads to a difficulty in preoperative diagnosis. Here, a pituitary adenoma and a suprasellar arachnoid cyst in the same patient is presented, and possible etiopathogenetic mechanisms and surgical treatment are discussed. CASE A 56-year-old male patient was admitted to t...

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ژورنال

عنوان ژورنال: Journal of Neurology, Neurosurgery & Psychiatry

سال: 1978

ISSN: 0022-3050

DOI: 10.1136/jnnp.41.1.83