pituitary apoplexy/heparin

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Heparin-Induced Pituitary Apoplexy Presenting as Isolated Unilateral Oculomotor Nerve Palsy: A Case Report and Literature Review.

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Pituitary apoplexy (PA) is a rare and potentially life-threatening clinical syndrome resulting from pituitary gland hemorrhage and/or infarction. Anticoagulation is a risk factor for triggering PA. Isolated oculomotor nerve palsy is an atypical presentation of

Pituitary metastasis presenting as ischemic pituitary apoplexy following heparin-induced thrombocytopenia.

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Pituitary apoplexy (PA) typically results from infarction or hemorrhage in a pituitary adenoma, while PA in nonadenomatous pituitary gland is uncommon. Prothrombotic states have never been recognized as precipitating factors for PA. The authors report a case of an elderly female who received

Heparin therapy for myocardial infarction: an unusual trigger for pituitary apoplexy.

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A 68-year-old man with coronary artery disease was admitted for chest pain and ventricular tachycardia. After electric cardioversion, therapeutic heparinization was started for myocardial ischemia and nontransmural infarction. On day 3, headache and fever developed, followed by an altered sensorium

Pituitary apoplexy after administration of heparin and isosorbide dinitrate.

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Pituitary apoplexy in the setting of coronary angiography.

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Pituitary apoplexy (PA) is a rare but potentially life-threatening event. Typically, it results from hemorrhage into a pituitary adenoma, although cases affecting the intact gland have been reported. PA may occur spontaneously or in a setting of certain diagnostic and therapeutic procedures. The

Pituitary apoplexy after anticoagulation for unstable angina.

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OBJECTIVE To describe a patient with an undiagnosed pituitary macroadenoma, in whom pituitary apoplexy developed after heparin anticoagulation for treatment of unstable angina. METHODS We chronicle the clinical course, treatment, and outcome in a 53-year-old woman with pituitary apoplexy. Potential

[A case of pituitary adenoma progressing to pituitary apoplexy on the occasion of cerebral angiography].

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A case of pituitary adenoma which had progressed from subclinical pituitary apoplexy to subacute pituitary apoplexy on the occasion of cerebral angiography is reported. A 29-year-old man, complaining of bitemporal hemianopsia, was admitted to our department. Plain skull X-p revealed enlargement and

Pituitary apoplexy following shoulder arthroplasty: a case report.

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BACKGROUND Pituitary apoplexy following a major surgical procedure is a catastrophic event and the diagnosis can be delayed in a previously asymptomatic patient. The decision on thromboprophylaxis in shoulder replacements in the absence of definite guidelines, rests on a careful clinical

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