Peritumoral cysts associated with pituitary macroadenoma
نویسندگان
چکیده
منابع مشابه
Spontaneous regression of one nonfunctioning pituitary macroadenoma associated with abnormal liver enzyme tests
Background: Nowadays, drug and observation are advised to patients with lymphocytic hypophysitis and in some cases with nonfunctioning pituitary macoadenoma, instead of surgery. Case presentation: In this article, we report a woman with nonfunctional pituitary macroadenoma and panhypopitutarism and negative criteria for lymphocytic hypophysitis associated with increased liver enzymes. After thr...
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Rubinstein-Taybi Syndrome (RSTS) is an autosomal dominant disorder that is classically characterized by prenatal and postnatal growth restriction, microcephaly, dysmorphic craniofacial features, broad thumbs and toes, and intellectual disability. We describe the first reported case of a pituitary macroadenoma associated with RSTS. A 39-year-old Caucasian female with a past medical history of RS...
متن کاملCase Report of a Pituitary Macroadenoma Treated With Artemether Artemether and Pituitary Macroadenoma
with radiation) is the most common treatment option. Treatment of adenomas with surgery alone is associated with a 9% risk of significant complications other than hypothyroidism. Additionally, there is a significant recurrence risk with surgical treatment alone. Park et al found a 5-year recurrence rate of 15.2% and a 10-year recurrence rate of 50.5% for 132 patients having nonfunctioning macro...
متن کاملPituitary Macroadenoma with Superior Orbital Fissure Syndrome
Introduction: Pituitary adenomas are benign tumours which arise within the anterior lobe (adenohypophysis) of the gland in the sella turcica. Lateral extension into the cavernous sinuses can result in involvement of intracavernous part of 3rd, 4th and 6th cranial nerves resulting in superior orbital fissure syndrome. Case Report: We report a case of pituitary macroadenomas in which the involvem...
متن کاملLymphocytic Hypophysitis Mimicking Pituitary Macroadenoma.
Lymphocytic hypophysitis is an inflammatory /autoimmune disorder that primarily involves the pituitary gland and the pituitary stalk. The common clinical presentations include headache, nausea, vomiting, fatigue, features of hypopituitarism and diabetes insipidus as well as diplopia, orbital pain and bitemporal hemianopia. We report a case of lymphocytic hypophysitis which presented as hemichor...
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ژورنال
عنوان ژورنال: Journal of Neurosurgery
سال: 2015
ISSN: 0022-3085,1933-0693
DOI: 10.3171/2014.12.jns141031