نتایج جستجو برای: prolactinoma

تعداد نتایج: 1318  

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...

Journal: :Journal of Diabetes & Metabolic Disorders 2013

2014
Yutaka OKI

The treatment of functioning pituitary adenoma (FPA) must achieve endocrinological remission as well as tumor size reduction. The first-line treatment of FPA except prolactinoma is transsphenoidal surgery (TSS). Medical treatments and/or radiation will be applied as adjuvant therapies succeeding to TSS. In patients with prolactinoma, dopamine agonists, especially cabergoline, are quite efficien...

2017
Rostam Poormousa Kaveh Haddadi Misagh Shafizad Sajjad Shafiee

Background & Aim: Pituitary adenomas are part of a dissimilar group of benign neoplasms. The development of endoscopic techniques for surgery of paranasal sinuses has increased the opportunity for an endoscopic approach with regard to the pituitary gland. Minimally invasive endoscopic pituitary surgery, in turn, permits a more thorough tumor resection and fewer associated surgical complications...

Journal: :Hormones 2014
Labrini Papanastasiou Stelios Fountoulakis Theodora Pappa Konstantinos Liberopoulos Dimosthenis Malliopoulos Athina Markou George Piaditis

OBJECTIVE Dopamine agonists (DA) are the treatment of choice in patients with macroprolactinomas. Brain and optic chiasm herniation are unusual complications following treatment with DA. REPORT We present a case of a giant prolactinoma complicated by visual deterioration following cabergoline treatment. A 42-year-old man was admitted with seizures, right visual loss and visual defect in the u...

2012
Carl Friedrich Classen Monika Mix Ulrike Kyank Christina Hauenstein Dieter Haffner

INTRODUCTION McCune-Albright syndrome is a complex inborn disorder due to early embryonal postzygotic somatic activating mutations in the GNAS1 gene. The phenotype is very heterogeneous and includes polyostotic fibrous dysplasia, typically involving the facial skull, numerous café-au-lait spots and autonomous hyperfunctions of several endocrine systems, leading to hyperthyroidism, hypercortisol...

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