Searchable abstracts of presentations at key conferences in endocrinology

ea0070ep303 | Pituitary and Neuroendocrinology | ECE2020

Metastasis of lung cancer to two different endocrine organs

Sebile Dökmetaș Hatice , Dökmetaș Meriç , Kılıçlı Fatih , Cila Ayșenur , Olmușçelik Oktay

Both pituitary and adrenal gland metastases of lung cancer are very rare. A 79-year-old male patient with diabetes mellitus and hypertension was admitted to our hospital because of a mass in the lungs of the thorax CT. TSH: <0.005 UIU/ml (0.27–4.2), free T4: 0.794 ng/dl (0.93–1.7). Other pituitary hormones were also examined: FSH: 0.708 mIU/ml (1.5–12.4), LH: <0.1 mIU/ml (1.7–8.6), prolactin: 12.7 ng/ml (4.04–15.2), total testosterone: &#6...

ea0070ep329 | Pituitary and Neuroendocrinology | ECE2020

A rare tumor at the adult of the hypophysis: Atipic teratoid rabdoid tumor

Sebile Dökmetaș Hatice , Çakır Aslı , Cila Ayșenur , Dökmetaș Meriç , Kılıçlı Fatih

Pituitary adenomas are the most common cause of pituitary lesions. Atypical teratoid rhabdoid tumors are rare aggressive tumors of the central nervous system and are generally seen in children younger than 2 years of age, but also rarely in adults. Only 18 cases have been reported with pituitary involvement to 2018. Median survival in these tumors in adults is 21 months and the cause of death is usually tumor recurrence or leptomeningeal spread. Although surgery, chemotherapy ...

ea0070ep339 | Pituitary and Neuroendocrinology | ECE2020

A case report: Pituitary granulomatosis with polyangiitis

Sebile Dökmetaș Hatice , Çavușoğlu Güneș , Kılıçlı Fatih , Can Meryem , Dökmetaș Meriç , Cila Ayșenur

Introduction: Granulomatosis with polyangiitis (GPA) is a systemic vasculitis with necrotizing granulomatous inflammation. Any organ including the pituitary can be involved. Here we report a patient diagnosed with GPA who had nearly complete resolution of pituitary mass after cyclophosphamide and methylprednisolone treatment.Case46 year old female patient was admitted to the hospital after being examined by several departments for ...

ea0070ep367 | Pituitary and Neuroendocrinology | ECE2020

Diagnosis of multiple endocrine neoplasia type 1 in a patient with hypercalcemia and hyperprolactinemia

Sebile Dökmetaș Hatice , Yıldırım Ayșegül , Kılıçlı Fatih , Cila Ayșenur

Multiple endocrine neoplasia type 1 is a rare autosomal-dominant disorder. The most common endocrine tumors are parathyroid tumors, which cause hyperparathyroidism and hypercalcemia. Other tumors of MEN 1 include pituitary tumors for example prolactinomas and enteropancreatic tumors such as gastrinomas, insulinomas, VIPomas, carcinoid tumors. We report a case of a 31 year old male with MEN 1 presenting hypercalcemia with complaints of fatigue and weakness. On further questioni...