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DIAGNOSTIC CRITERIA OF GLIOMA OF THE PONS. YUN SHANG HUANG 1 1the 1st Surgical Division, Kyoto University Medical School pp.188-191
Published Date 1953/7/1
DOI https://doi.org/10.11477/mf.1406200352
  • Abstract
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 On the assumption that a glioma of the pons is a subependymal cell plate glioma originating from the "cell rests" in the floor of the fourth ventricle and near the midline, it would readily be understood why paresis of the abducens nerve (s) and/or weakness (or spasm) of the facial nerve (s) (double vision, squint, facial spasm and asymmetry of the face) should appear in a great majority of the cases as initial or early sings. And the chronology of the appearance of symptoms in the glioma under consideration will theoretically be in the order given as follows: paresis of the abducens and/or facial nerves (or facial spasm), weakness (or spasm) of the masseter muscle (s). drooping of the saliva and/or abnormal lacrimation, disturbance in the sense of taste, paresis of the sensory trigeminal nerve (s) and its nucleus, signs of dysfunction of the eighth cranial nerve (s) and its nuclei (ringing ears, reduction in the acoustic acuity, etc.), sings of cerebellar involvement and pyramidal signs. However, the signs of involvement of those nerve fibers, which have a decussation, such as the central trigeminal lemiscus, the trabezoid body, the pathways to and from the cerebellum, etc., may possibly appear earlier than the order described above. Neurologic examination will usually disclose multiple involvement of the cranial nerves (nuclei) and cerebellar signs on one side or bilaterally and contralateral (or bilateral) pyramidal signs. But signs of increased intracranial pressure (choked discs) may often be absent.

 Not only symptomatologically, the tegmen of the pons was seen, in most cases of gliomas of pons hitherto reportee by various authors and of our own, to be either completely destroyed or, at least, invaded by the tumor mass; a fact which seems to justify the hypothesis that a glioma of the pons is a subependymal cell plate glioma.

 Furthermore, by the analogy in the age incidence of a cerebellar astrocytoma with that of a pons-glioma may it be conclusively explained that the latter tumor is a kind of subependymal cell plate gliomas, since the former, which can be considered as a subependymal cell plate glioma in the roof of the fourth ventricle, occurs most frequently in children under the age of ten years while this is likewise the case in a glioma of the pons.

 In summarizing, a diagnosis of glioma of the pons can easily and unmistakably be made when the age of the patient, the initial or early signs, the chronology of the appearance of symptoms and an absence of choked discs and other neurologic findings are carefully taken into consideration as (differential-) diagnostic criteria.


Copyright © 1953, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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