Acromegaly remission, SIADH and pituitary function recovery after macroadenoma apoplexy
Autor: | S Sarria-Estrada, Fuat Arikan, Betina Biagetti, E Sanz-Sapera |
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Rok vydání: | 2019 |
Předmět: |
Male
LH Pediatrics Hydrocortisone Endocrinology Diabetes and Metabolism Infarction Spontaneous remission White Hypopituitarism Gynaecomastia lcsh:Diseases of the endocrine glands. Clinical endocrinology Pituitary haemorrhage Cortisol Dexamethasone 0302 clinical medicine FSH Testosterone FT4 Podiatry Fatigue TSH Concentration difficulties Hyponatraemia IGF1 SIADH Headache Pituitary apoplexy Saline GH Fluid restriction July 030220 oncology & carcinogenesis Feet - increased size medicine.drug MRI Dexamethasone suppression ACTH stimulation Adult CT scan medicine.medical_specialty Thyroxine (T4) 030209 endocrinology & metabolism 03 medical and health sciences Pituitary adenoma Fluid repletion Acromegaly Internal Medicine medicine Glucocorticoids lcsh:RC648-665 business.industry Sodium medicine.disease Antidiuretic Hormone Unique/Unexpected Symptoms or Presentations of a Disease Hypertonic saline Pituitary Spain business Serum osmolality |
Zdroj: | Endocrinology, Diabetes & Metabolism Case Reports Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2019) |
ISSN: | 2052-0573 |
Popis: | Summary Pituitary apoplexy is a rare but potentially life-threatening clinical syndrome characterised by ischaemic infarction or haemorrhage into a pituitary tumour that can lead to spontaneous remission of hormonal hypersecretion. We report the case of a 50-year-old man who attended the emergency department for sudden onset of headache. A computed tomography (CT) scan at admission revealed pituitary haemorrhage and the blood test confirmed the clinical suspicion of acromegaly and an associated hypopituitarism. The T1-weighted magnetic resonance imaging (MRI) showed the classic pituitary ring sign on the right side of the pituitary. Following admission, he developed acute-onset hyponatraemia that required hypertonic saline administration, improving progressively. Surprisingly, during the follow-up, IGF1 levels became normal and he progressively recovered pituitary function. Learning points: Patients with pituitary apoplexy may have spontaneous remission of hormonal hypersecretion. If it is not an emergency, we should delay a decision to undertake surgery following apoplexy and re-evaluate hormone secretion. Hyponatraemia is an acute sign of hypocortisolism in pituitary apoplexy. However, SIADH although uncommon, could appear later as a consequence of direct hypothalamic insult and requires active and individualised treatment. For this reason, closely monitoring sodium at the beginning of the episode and throughout the first week is advisable to guard against SIADH. Despite being less frequent, if pituitary apoplexy is limited to the tumour, the patient can recover pituitary function previously damaged by the undiagnosed macroadenoma. |
Databáze: | OpenAIRE |
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