Back in 1998, a then 44-year-old male patient presented with a left hemispheric minor ischemic stroke of undefined cause and was diagnosed by DSA with a small, right-hand asymptomatic yet partially thrombosed true posterior communicating artery (TPcomA) aneurysm. The patient failed to regularly attend the assigned follow-up clinical and crosssectional imaging examinations. In 2016, 18 years after the first DSA examination, the patient presented with progressive left-hand hemiparesis and mild fluctuating central facial nerve palsy. Cranial non-contrast-enhanced computed tomography (NCCT) revealed the presence of a large lobulated and partially thrombosed right-hand TPcomA aneurysm. The thrombotic material in the aneurysmal sac was exerting a local mass effect on the thalamus and brainstem. Contralateral ischemic changes in the left-hand capsular region were also noted. Diagnostic angiography confirmed that the lobulated aneurysm originated from the right-hand "fetal" PcomA itself. In 1998, as well as in 2016, the patient clearly rejected all the treatment options offered. Another 2 years later, the patient presented with a worsening of his left-hand hemiparesis. A cranial MRI and the following DSA examination confirmed that the aneurysm had been progressively growing over the past two