Following a dramatic change of its reported incidence, it was only recently
recognized that acquired crossed aphasia in dextral children represents a
highly exceptional phenomenon. We describe in a three epoch time-frame mode
l the aphasic and neurocognitive manifestations of an additional case and f
ocus briefly on its anatomoclinical configurations. In our patient, a right
parietal cortico-subcortical hemorrhagic lesion caused an initially severe
aphasia. After remission of the global aphasic symptoms in the acute phase
, an adynamic output disorder with relatively severe auditory-verbal compre
hension disturbances developed. In addition to the adynamia of self generat
ed speech, formal language investigations performed 3 weeks postonset, reve
aled agrammatism, hypertonic dysarthria, and dysprosodia. A substantial imp
rovement of the aphasic disorder was objectified 83 days postonset. Neurops
ychological investigations disclosed both dominant and nondominant hemisphe
re dysfunctions. Reassess ment of neurocognitive functions after a 10-year
period evidenced discrete residual anemia, confined to visual confrontation
al naming and a discrete visuo-perceptual syndrome. Given the posterior loc
alization of the lesion, the syndrome shift from global to predominantly ad
ynamic aphasia represents a finding beyond the plausible anatomoclinical ex
pectations holding in general for the uncrossed, classic types of childhood
and adult aphasia. As the first representative of crossed aphasia in dextr
al children with an anomalous lesion-aphasia profile, our case provides evi
dence to enrich the discussion on lateralization and intrahemispherical org
anization of language functions in both childhood and adult aphasia. (C) 20
01 Academic Press.