Aldosterone producing adenoma (APA) is a rare but potentially curable form
of paediatric hypertension. We report a case of APA in a 9-year-old boy, su
spected due to persistent hypokalaemia. Neither BP nor initial laboratory i
nvestigations disclosed the diagnosis and the presence of an APA was sugges
ted by functional tests and radiological findings. Histologically, a cortic
al tumour was found associated with a marked medullary hyperplasia of both
chromaffin and ganglion cells.
Conclusion This case reinforces the need for further investigations in pati
ents with misleading clinical and laboratory data.