Meyer B et al.(1996) Pure word deafness after resection of a tectal plate glioma with preservation of wave V of brain stem auditory evoked potentials.
Masuda S et al. (2000) Word deafness after resection of a pineal body tumor in the presence of normal wave latencies of the auditory brain stem response.
Johkura K, et al.(1998) Defective auditory recognition after small hemorrhage in the inferior colliculi.
Pan CL et al. (2004)Auditory agnosia caused by a tectal germinoma.
Hu CJ et al. (1997) Traumatic brainstem deafness with normal brainstem auditory evoked potentials.
Vitte E, et al.(2002) Midbrain deafness with normal brainstem auditory evoked potentials.
Coslett HB et al. (1984) Pure word deafness after bilateral primary auditory cortex infarcts.
Denes G, Semenza C. (1975) Auditory modality-specific anomia: evidence from a case of pure word deafness.
Cocito D et al.(1990) Hematoma of the inferior colliculus: uncommon cause of trochlear nerve deficit and contralateral sensory hemisyndrome.
Champoux F et al. (2007). Auditory processing in a patient with a unilateral lesion of the inferior colliculus.
Hashimoto T et al. (1995) Development of the brainstem and cerebellum in autistic patients.
Gaffney GR et al. (1988) Morphological evidence for brainstem involvement in infantile autism.
Abell F et al. (1999) The neuroanatomy of autism: a voxel-based whole brain analysis of structural scans.
Aylward EH et al. (1999) MRI volumes of amygdala and hippocampus in non-mentally retarded autistic adolescents and adults.
Elia M et al. (2000) Clinical correlates of brain morphometric features of subjects with low-functioning autistic disorder.
Simon EN. (2005)Auditory agnosia caused by a tectal germinoma.
5 - Word deafness and the inferior colliculi At least thirteen cases have been reported, of loss of speech understanding following bilateral damage of the inferior colliculi, all in people with previously normal language. The case reports are summarized in chapter 8 above. Inability to understand spoken language is often referred to as "word deafness." Meyer et al. (1996) and Masuda et al. (2000) reported loss of speech comprehension following accidental destruction of the inferior colliculi during surgery for removal of tumors [1, 2]. Johkura et al. (1998) reported a case of traumatic injury to the inferior colliculi suffered in a skiing accident [3].
In December 2004 Pan et al. reported auditory agnosia in a young boy who developed a cancerous growth of the midbrain that involved both inferior colliculi [4]. Removal of the abnormal tissue was successful in this case, with slow but steady recovery of auditory discrimination. Pan et al. cited the cases of Meyer et al., Masuda et al., and Johkura et al., plus those of Hu et al. (1997) and Vitte et al. (2002) [5, 6].
The case reported by Hu et al. was the result of traumatic injury in a motor vehicle accident [5]. Vitte et al. reported two cases, one the result of head injury, the other from hemorrhage following surgery [6].
Meyer et al. commented that they were aware of three other cases of pure word deafness with lesions restricted to the inferior colliculi, but did not give citations to other published reports [1]. Johkura et al. reviewed the literature on verbal auditory agnosia, first reported with left temporal lobe damage that disconnected the language receptive area from subcortical auditory input and inputs across the corpus callosum from the right temporal lobe. Later it was found that verbal auditory agnosia most often involved bilateral temporal lobe damage, or disruption of the auditory pathway from the medial geniculate bodies of the thalamus [7, 8]. The cases of word deafness following damage of the inferior colliculi in the 13 case reports above, indicate that disruption even at the midbrain level can interfere with language comprehension.
Word deafness results only from bilateral damage of the inferior colliculi [9, 10]. Champoux et al. (2007) did extensive testing of a 12-year-old child with traumatic injury of the right inferior colliculus. The child did not display any neurological dysfunction, but speech comprehension was impaired in the presence of competing sounds.
Loss of function within the inferior colliculi present from birth might be expected to prevent acquisition of language through the normal channel of hearing. Lesions of the inferior colliculi caused during a traumatic birth might be visible in MRI scans, but might also be overlooked when clear-cut damage to wider areas of the brain are evident.
Impairment of function without visible damage within the inferior colliculi probably would not be seen in MRI scans. However, decreased volume of brainstem areas in individuals with autism have been determined by measurements of MRI scans [11-15]. This evidence supports the usefulness of considering the perinatal vulnerability of brainstem nuclei, and impaired function of the inferior colliculi in the developmental language disorder of children with autism. In their reply to my letter on auditory agnosia resulting from a germinoma growth into the tectum, Pan and Hsieh commented:
"Previous studies on structural abnormalities in pervasive developmental disorders were hampered by inadequate anatomical resolution of conventional imaging tools. Functional disturbances without obvious anatomical changes are likely to be overlooked in some of these conditions. With the advance of neuroimaging techniques, particularly the magnetic resonance imaging, these hypotheses are ready to be tested" [16, p339].
Auditory functions required to extract meaning from spoken language should be a primary focus of research in autism. Results of existing diverse studies of the auditory system may be useful although most such research was not about autism.
Meyer B, Kral T, Zentner J. (1996) Pure word deafness after resection of a tectal plate glioma with preservation of wave V of brain stem auditory evoked potentials. Journal of Neurology, Neurosurgery and Psychiatry. 61:423-4.
Masuda S, Takeuchi K, Tsuruoka H, Ukai K, Sakakura Y. (2000) Word deafness after resection of a pineal body tumor in the presence of normal wave latencies of the auditory brain stem response. The Annals of otology, rhinology, and laryngology. 2000 Dec;109(12 Pt 1):1107-12.
Johkura K, Matsumoto S, Hasegawa O, Kuroiwa Y. (1998) Defective auditory recognition after small hemorrhage in the inferior colliculi. Journal of the Neurological Sciences. 161:91- 6.
Pan CL, Kuo MF, Hsieh ST. Auditory agnosia caused by a tectal germinoma. Neurology. 2004 Dec 28;63(12):2387-9.
Hu CJ, Chan KY, Lin TJ, Hsiao SH, Chang YM, Sung SM. (1997) Traumatic brainstem deafness with normal brainstem auditory evoked potentials. Neurology 1997;48:1448–1451.
Vitte E, Tankéré F, Bernat I, Zouaoui A, Lamas G, Soudant J. Midbrain deafness with normal brainstem auditory evoked potentials. Neurology 2002;58:970–973.
Coslett HB, Brashear HR, Heilman KM. Pure word deafness after bilateral primary auditory cortex infarcts. Neurology 1984;34:347–52.
Denes G, Semenza C. Auditory modality-specific anomia: evidence from a case of pure word deafness. Cortex 1975;11:401–11.
Cocito D, Amedeo G, Gallo G, Vischia F, De Lucchi R. Hematoma of the inferior colliculus: uncommon cause of trochlear nerve deficit and contralateral sensory hemisyndrome. Ital J Neurol Sci. 1990 Feb;11(1):71-4.
Champoux F, Paiement P, Mercier C, Lepore F, Lassonde M, Gagne JP.Auditory processing in a patient with a unilateral lesion of the inferior colliculus. Eur J Neurosci. 2007 Jan;25(1): 291-7.
Hashimoto T, Tayama M, Murakawa K, Yoshimoto T, Miyazaki M, Harada M, Kuroda Y (1995) Development of the brainstem and cerebellum in autistic patients. Journal of Autism and Developmental Disorders 25:1-18.
Gaffney GR, Kuperman S, Tsai LY, Minchin S (1988) Morphological evidence for brainstem involvement in infantile autism. Biological Psychiatry 24:578-586.
Abell F, Krams M, Ashburner J, Passingham R, Friston K, Frackowiak R, Happe F, Frith C, Frith U. (1999) The neuroanatomy of autism: a voxel-based whole brain analysis of structural scans. Neuroreport. 10:1647-51
Aylward EH, Minshew NJ, Goldstein G, Honeycutt NA, Augustine AM, Yates KO, Barta PE, Pearlson GD. (1999) MRI volumes of amygdala and hippocampus in non-mentally retarded autistic adolescents and adults. Neurology. 53:2145-50.
Elia M, Ferri R, Musumeci SA, Panerai S, Bottitta M, Scuderi C. Clinical correlates of brain morphometric features of subjects with low-functioning autistic disorder. J Child Neurol. 2000 Aug;15(8):504-8.
Simon EN. Auditory agnosia caused by a tectal germinoma. Neurology. 2005 Jul 26;65(2): 339; author reply 339.