GP39 A case series of suspected congenital adrenal hyperplasiain one week in a regional endocrine unit. (June 2019)

• Record Type: Journal Article
• Authors: Agrawal, Pankaj; McCann, Aisling; Conlon, Kevin; Reynolds, Claire; Joyce, Caroline; Taylor, Norman; O'Riordan, Stephen MP
• Is Part Of: Archives of disease in childhood. Volume 104:Supplement 3(2019)
• Page Start: A45
• Page End: A45
• Publication Date: 2019-06
• Subjects: Infants -- Diseases -- Periodicals; Newborn infants -- Diseases -- Periodicals; Fetus -- Diseases -- Periodicals; 618.920105
• DOI: 10.1136/archdischild-2019-epa.105
• Languages: English
• ISSNs: 1359-2998

Abstract

Abstract : Congenital adrenal hyperplasia (CAH) is the most common cause of salt wasting during infancy. During workup other rarer causes should also be considered. We report three cases of suspected CAH, aiming to highlight that CAH is not always the cause of adrenal insufficiency. Case 1: A two-week-old term female born to non-consanguineous parents, presented with failure to thrive, hyponatremia, Na 118 mmol/L (132–144 mmol/L), hyperkalaemia, K 7.2 mmol/L (3.5–5.1 mmol/L), plasma (am) cortisol 134 nmol/L (101–536 nmol/L). A diagnosis of CAH was considered and Hydrocortisone (HC), Fludrocortisone and Sodium Chloride (NaCl) (30%) were commenced. Urinary steroid profile (USP) was sent to Kings College, London diagnosing Aldosterone Synthase Deficiency (ASD) type I, prompting to stop HC and to continue Fludrocortisone. Further testing showed high renin >300 pg/ml/hour (normal <61 pg/ml/hour), low aldosterone 50 pg/ml (normal >300–1900 pg/ml). 17-OH Progesterone and Adrenocorticotropic-hormone (ACTH) were normal. Case 2: A term 3.7 kg female, antenatally diagnosed bilateral cleft lip & palate, delivered by cesarean-section, to 44-year-old primi mother was admitted to NICU on day-3 with low Sodium 122 mmol/L (132–144 mmol/L), high Potassium 6.2 mmol/L (3.5–5.1 mmol/L) normal Cortisol (am) 377nmol/L (101–536nmol/L), serum/urine osmolality. CAH was suspected and HC, Fludrocortisone and NaCl (30%) were commenced. MRI brain showed partial agenesis of corpus callosum, with normal pituitary. Further investigations: am cortisol: 85 nmol/L (101–536nmol/L), ACTH (am): 23.1 pmol/L (1.1–13.2pmol/L), aldosterone, renin, 17 OH progesterone, USP, urine-biochemistry, LH, FSH, B-HCG, AMH, TFT's & Blood glucose were normal. Microarray-CGH showed 16p13.11 microdeletion (Father same deletion), karyotype 46XX. Trial of stopping Fludrocortisone & NaCl (30%) was unsuccessful and NaCl (30%) was recommenced. She failed a synachten test and remains on HC and NaCl (30%). Current diagnosis is adrenal insufficiency related to 16p13.11 microdeletion. Case 3: A term 23 day old male was transferred to Cork University Hospital (CUH) from a peripheral hospital with 12 hours of projectile, non-bilious vomiting. On examination he was dehydrated, unwell, with hyper-pigmented scrotum (normal descended testes) and normal phallus. Initial tests revealed hyponatremia, Na 108 mmol/L (132–144 mmol/L), & hyperkalemia, K 6.9 mmol/L (3.5–5.1 mmol/L). CAH was suspected and HC (8–10 mg/m 2 /day), Fludrocortisone 200mcg & NaCl (30%) were commenced. 17-OH progesterone was >400 nmol/L (<4nmol/L). Genetic tests confirmed a diagnosis of CAH secondary to 21-hydroxylase deficiency. Conclusion: All three cases presented within a week in CUH with acute adrenal insufficiency with salt wasting, thought to be CAH. However; only one was confirmed CAH. During the workup, USP and genetic testing were key to distinguish these rarer diagnoses.