Pituitary Teratoma Presenting as Central Diabetes Insipidus with a Normal MRI Finding

Abstract

Dear Sir, Central diabetes insipidus (DI) is a diverse condition characterized by polydipsia and polyuria due to a defect of arginine vasopressin. Known conditions for this disorder include inflammatory, autoimmune, traumatic brain injury, and brain tumors. Brain tumors such as craniopharyngioma1 and germinoma2 are associated with Central DI. Up to 50 percent of cases of central DI are thought to be idiopathic in nature.3,4 Herein we describe an interesting case of a 17-year-old man who was diagnosed with central DI, initially thought to be idiopathic but found to have pituitary teratoma. A 17-year-old male was admitted to our hospital with a 4-month history of polyuria and polydipsia with severe thirst. Initial laboratory work revealed serum BUN 8.4 mg/dL, creatinine 0.65 mg/dL, sodium 147 mEq/l, potassium 3.9 mEq/L, chloride 108 mEq/L, calcium 9.1 mg/dL, phosphate 4.6 mg/dL, fasting plasma glucose 109 mg/dL, and hemoglobinA1C 6.0%. A thyroid function test was normal. Plasma osmolarity was 291 mOsm/kgH2O and urinary osmolarity was 79 mOsm/kgH2O. His urine output was 4 to 5 liters per day without glycosuria. Urine osmolarity increased from 115 to 297 mosm/Kg H2O after 6 hours of water deprivation. Two hours later, urine osmolarity was still under 300 mosm/KgH2O (296 mosm/KgH2O) and the serum level of the antidiuretic hormone (ADH) level was < 0.4 pg/mL. After using nasal spray with 1-desamino-8-D-arginine vasopressin (DDAVP) 10 µg, his urine osmolarity increased from 296 to 600 mosm/KgH2O. His clinical course and laboratory finding led us to suspect Central DI. No abnormality was detected in a brain MRI (Fig. 1A). A complete work-up result to find the cause of Central DI was negative and his central DI was thought to be due to idiopathic cause. Fig. 1 (A) Initial brain MRI showed normal signal intensity in the posterior pituitary gland. (B) Follow-up MRI showed 3.3 cm sized lobulated solid mass on the sella and supurasellar area involving hypothalamus and optic chiasm. He was treated with 10 µg of desmopressin nasal spray every night. His urine volume decreased to around 2 L/day. He was discharged with DDAVP and was followed monthly in an outpatient clinic. After 45 months, he presented with a headache and diplopia persisting for 1 month. A brain MRI was completed, which showed a 3.3 cm sized lobulated solid mass involving the sellar and suprasellar area (Fig. 1B). He underwent a transspenoidal excision biopsy and the biopsy result was confirmed by pituitary teratoma. He received chemotherapy and radiation therapy. Magnetic resonance imaging (MRI) is the best imaging technique for detecting subtle abnormalities of the hypothalamic-pituitary region.5 Idiopathic central DI is a diagnosis of exclusion, and is diagnosed when central DI occurs in the absence of any alteration that is known to be responsible for DI.2,5 Central DI can precede overt brain tumors. Therefore, even though idiopathic central DI is diagnosed initially with a normal brain MRI, we may need a periodic clinical follow-up and thus serial brain MRIs to detect occult brain lesions.2,6