1931
DOI: 10.1001/archneurpsyc.1931.02230110003001
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Adamantinoma of the Craniopharyngeal Duct

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Cited by 58 publications

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“…Modern knowledge allows us to say that certain signs and symptoms are specific evidence of dysfunction of the optic chiasma, while other signs point with equal certainty to the pituitary or hypothalamus, but overlying these, and pwsibly altering the balance between such regionally determined factors, there can be the general effort of increased intracranial pressure, whether by mere growth of the tumour or by varied degrees of blockage to the flow of cerebrospinal fluid. The varied syndromes thus encountered are available in the scattered case reports and reviews, especially those of Critchley and Ironside (1926), Beckmann and Kubie (1929), Frazier and Alpers (1931), Cushing (1932) and Friedgood (1946). The anienorrhma, polyuria, abnormal drowsiness and optic atrophy of the present case are all of common occurrence in adult patients.…”
Section: Discussion
mentioning
confidence: 99%
“…There is likewise difference in behaviour from case to case. It is thus rather difficult to produce a satisfactory classification of the tumours taking origin from the embryonic craniopharyngeal canal (Duffy, 1920 ;Frazier and Alpers, 1931 ;Friedgood, 1946) and it is obvious that with increasing knowledge the suggested categories are having to be modified and subdivided. What may be called the typical para-pituitary adamantinoma or basal-cell carcinoma, of which t,he present case is a good example, is only locally invasive ; it is usually solid, although multiple cysts may be present, especially if the tumour itself be large.…”
Section: Discussion
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confidence: 99%
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