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Complains:
polyuria-polydipsia with onset about 6-7 wks ago(6-8 l/24h) cronic fatigue syndrome constipation
Family history: Her parents with cardiac pathology Personal history: without a history of significant pathological Non smoker No chronic medication use Course of the disease: The patient without significant previous history accuses polydipsia (6 8 l / 24h) and polyuria wich appeared insidious about 6-7 weeks ago, with progressive character associated with fatigue and constipation.
Clinical exam
Expressive face Normal skin color H: 174 cm; W: 76,5 kg; BMI: 25,33 kg/m Muscles weakness. BP: 110/80 mmHg, HR: 70/min Gastrointestinal app.: polydipsia,constipation Genitourinary app.: polyuria, nicturia
Endocrine system
Hypothalamo-pituitary system: Pituitary tumor syndrome:
neurological syndrome: no signs or symptoms opto-chiasmatic syndrome: no signs or symptoms imagistic findings: discussed at paraclinical findings endocrine syndrome: polyuria-polydipsia, nicturia
Thyroid gland: normal size and consistency Parathyroid glands: constipation, muscle weakness Adrenal glands: muscle weakness
Presumptive diagnosis:
Polyuro-polydipsic syndrome
Lab tests
Blood Count: Leuc: 6.600/ml, Hgb 16.1 g/dl, Htc 49.4 %, PLT 268.000 ml, Ionogram: Ca total : 11,3 mg/dl , P: 2.18 mg/dl , Mg: 2.09 mg/dl ; Na: 144 mmol/l; K: 4.1 mmol/l Total cholesterol: 193 mg/dl; triglycerids: 110 mg/dl Glycemia: 89 mg/dl . Uric acid: 6.11 mg/dl Creatinine: 0.88 mg/dl, Uree: 23.4 mg/dl Normal liver enzymes. Alkaline phosphatase: 182 u/l Urinary balance sheet: Bil: neg, UBG: normal, KET: neg, ASC: neg, GLU: normal, PROT: neg, ERY: neg, PH: 6, Density: 1000; Urinary Ca : 456.24 mg/24 h , Urinary P: 998.16 mg/24 h
Hormonal assessment
PTH: 120.9 pg/ml (15-65)
Ca total : 11.3 mg/dl, P:2.18mg/dl, Magnesium: 2.09 mg/dl
TSH: 1.27 UI/ml (0.38-4.31) FT4: 0.91 ng/dl (0.82-1.63) Cortisol 8 am: 16.4 g/dl PRL: 7.06 ng/ml
Lab tests
Urine output (ml) 980 680 USG 1.000 1.001
580
760 830 630 710 510
1000
1.000 1.000 1.000 1.000 1.000
1100
880 650 1100 910
1.000
1.000 1.000 1.000 1.000
180
1.025
Paraclinical examination
Thyroid ultrasound:
Right lobe: 16/17.5/40 mm, volume 5.8 ml, with a posterocaudal nodule hypoechoic 9,5 x 21.5 mm, with hypervascularization Left lobe 12.5/ 18.4/ 39.5 mm, volume 4,87 ml. Istm: 4 x 7 mm, inhomogeneous structure without nodular formations
Paraclinical examination
Sestamibi with 99mTc Parathyroid Scintigraphy :
Parathyroid adenoma in the lower pole of the right lobe (~20/10mm), with high metabolic activity.
Paraclinical examination
Cranian MRI focused on hypothalamic-pituitary system
- a lesion about 2,5 mm in diameter, slightly hypointense compared to normal pituitary tissue, located in the left lob of the pituitary gland.
Final diagnosis
o Central Diabetes Insipidus o Pituitary Microadenoma o Primary hyperparathyroidism o Parathyroid adenoma o Multiple endocrine neoplasia MEN 1 ?
Differential diagnosis
Other causes of polyuria - polydipsia syndrome :
- Diabetes mellitus - Nephrogenic DI - Primary polydipsia
Secondary Hyperparatiroidism- causes: - Renal failure, decreased calcium intake, calcium malabsortion- vitamin D
deficiency, bariatric surgery, celiac disease; loop diuretics.