A rare cause of severe Cushing's syndrome.

2020 ACTH Adrenal Adrenalectomy Adult Alpha-blockers Amlodipine Antibiotics Anticoagulants* Arthralgia Beta-blockers Blood pressure CT scan Calcium Cardiology Catecholamines (plasma) Co-trimoxazole* Cortisol Cortisol (serum) Cushing's syndrome Dexamethasone suppression Diabetes mellitus type 1 Diarrhoea Echocardiogram Glucocorticoids Glucose (blood) Haematoxylin and eosin staining Heart rate Histopathology Hyperactivity Hypercortisolaemia Hyperglycaemia Hyperpigmentation Hypertension Hypokalaemia Insight into disease pathogenesis or mechanism of therapy Insulin Laparoscopic adrenalectomy Malaise Male March Metanephrines Metanephrines (plasma) Metyrapone Normetanephrine Palpitations Phaeochromocytoma Phenoxybenzamine Potassium Potassium chloride Prednisolone Propranolol Resection of tumour Tremulousness United Kingdom Ventricular hypertrophy Vitamin D Vomiting Weight gain White

Journal

Endocrinology, diabetes & metabolism case reports
ISSN: 2052-0573
Titre abrégé: Endocrinol Diabetes Metab Case Rep
Pays: England
ID NLM: 101618943

Informations de publication

Date de publication:
13 Mar 2020
Historique:
received: 21 02 2020
accepted: 26 02 2020
pubmed: 14 3 2020
medline: 14 3 2020
entrez: 14 3 2020
Statut: aheadofprint

Résumé

Ectopic adrenocorticotropic hormone (ACTH) production is an uncommon cause of Cushing's syndrome and, rarely, the source can be a phaeochromocytoma. A 55-year-old man presented following an episode of presumed gastroenteritis with vomiting and general malaise. Further episodes of diarrhoea, joint pains and palpitations followed. On examination, he was hypertensive with no clinical features to suggest hypercortisolaemia. He was subsequently found to have raised plasma normetanephrines of 3.98 nmol/L (NR <0.71) and metanephrines of 0.69 nmol/L (NR <0.36). An adrenal CT showed a 3.8 cm right adrenal nodule, which was not MIBG-avid but was clinically and biochemically consistent with a phaeochromocytoma. He was started on alpha blockade and referred for right adrenalectomy. Four weeks later, on the day of admission for adrenalectomy, profound hypokalaemia was noted (serum potassium 2.0 mmol/L) with non-specific ST-segment ECG changes. He was also diagnosed with new-onset diabetes mellitus (capillary blood glucose of 28 mmol/L). He reported to have gained weight and his skin had become darker over the course of the last 4 weeks. Given these findings, he underwent overnight dexamethasone suppression testing, which showed a non-suppressed serum cortisol of 1099 nmol/L. Baseline serum ACTH was 273 ng/L. A preliminary diagnosis of ectopic ACTH secretion from the known right-sided phaeochromocytoma was made and he was started on metyrapone and insulin. Surgery was postponed for 4 weeks. Following uncomplicated laparoscopic adrenalectomy, the patient recovered with full resolution of symptoms. Phaeochromocytomas are a rare source of ectopic ACTH secretion. A high clinical index of suspicion is therefore required to make the diagnosis. Ectopic ACTH secretion from a phaeochromocytoma can rapidly progress to severe Cushing's syndrome, thus complicating tumour removal. Removal of the primary tumour often leads to full recovery. The limited literature suggests that the presence of ectopic Cushing's syndrome does not appear to have any long-term prognostic implications.

Identifiants

pubmed: 32168466
doi: 10.1530/EDM-20-0011
pii: EDM200011
pmc: PMC7077516
doi:
pii:

Types de publication

Journal Article

Langues

eng

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Auteurs

Shamaila Zaman (S)

Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.

Bijal Patel (B)

Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.

Paul Glynne (P)

The Physicians' Clinic, London, UK.

Mark Vanderpump (M)

The Physicians' Clinic, London, UK.

Ali Alsafi (A)

Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.

Sairah Khan (S)

Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.

Rashpal Flora (R)

Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.

Fausto Palazzo (F)

Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.

Florian Wernig (F)

Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.

Classifications MeSH