über Knorpelgeschwülste der SchÄdelbasis mit intrakranieller Ausdehnung

Klingler, Marco

doi:10.1007/bf01577680

Cited by 29 publications

(7 citation statements)

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“…Most bas al chondromas see m to originale in the a re a near the sutu re lines in th e body of th e sphe noid bone. the apex of th e petro us-t emporal bon e and the bast -occiput of th e occipital bone (23). The path ogen esis of basal chondroma s is mu ch c1eare r th an that of the ircounte rparts ove r th e ce re bra l convex-Wes (38).…”

Section: Discussfonmentioning

confidence: 99%

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Sellar chondroma in a case of Ollier's disease

Pospiech

Mehdorn²,

Reinhardt³

et al. 1989

Minim Invasive Neurosurg

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Section: Discussfonmentioning

confidence: 99%

“…As already mentioned above, it is. however, often impossible to ascerta in the exact site of or igin (23,26,39) . Nevertheless, intrasellar chondromas see m to have some common elinical features like chiasmatic syndrom e an d impairment of'vtston.…”

Section: Discussfonmentioning

confidence: 99%

Sellar chondroma in a case of Ollier's disease

Pospiech

Mehdorn²,

Reinhardt³

et al. 1989

Minim Invasive Neurosurg

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“…Chondromas of the pontine angle have been the commonest of the chondromas of the posterior fossa ; only one chondroma situated in the clivus has been reported (KLINGLER 1951).…”

mentioning

confidence: 99%

Roentgenologic Findings in Chondromas of the Pontine Angle

Roukkula¹

1964

Acta Radiologica. Diagnosis

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“…Impairment of certain cranial nerves may also be present, but because of the insidious involvement, diagnosis is usually made late when the tumour is of advanced size. The clinical manifestations of chondromas of the base have been described separately by List (1943) and Klingler (1951). Of the medial tumours the suprasellar lesion will cause visual defects such as bitemporal hemianopsia, optic atrophy, and diminished visual acuity due to compression of the optic chiasm and optic tracts.…”

mentioning

confidence: 99%

Primary non-skeletal intracranial cartilaginous neoplasms: report of a chondroma and a mesenchymal chondrosarcoma

Lapi

1970

Journal of Neurology, Neurosurgery & Psychiatry

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Primary intracranial cartilaginous neoplasms which do not arise from bones of the skull are extremely rare (Alpers, 1935;Chorobski, Jarzymski, and Ferens, 1939;Dahlin and Henderson, 1962;Flyger, Freidenfeldt, and Orell, 1963;Siris and Angrist, 1942). We report herein two such tumours; one benign and the other malignant.CASE 1: CHONDROMA During the seventh month of pregnancy L.W., a 32-yearold white woman, began to exp-rience fainting spells of 15 minutes' duration followed by increasingly severe speech difficulty and weakness in the right arm. She was admitted to the hospital approximately one month after delivery, or three months after the onset of symptoms, at which time she was having generalized convulsions, bit her tongue, and lost consciousness for a 30 minute period.The past history, family history, and system review were negative or non-contributory except as related to the present illness.Physical examination revealed a well-developed, wellnourished, white female with mild speech slurring. There was a contusion in the right frontal region of the scalp.The fundi showed slight blurring of the nasal and upper disc margins and the pupils were equal and reacted to light. Right hemiparesis with hyperactive reflexes on the right was present. Hoffman's sign was positive on the right, but the Babinski reaction was negative. There was no astereognosis.Moderate nasal obstruction with yellowish nasal discharge was noted. Artificial dentures were well-fitting and oral hygiene was good. The breasts were full and lactating. The physical examination was otherwise negative and the blood pressure was 130/70 mm Hg.Radiographs of the skull showed a shell-like calcification on the left just posterior to the coronal suture and in the region of the middle meningeal vessels, the grooves of which appeared more pronounced on the left. The adjacent skull was thickened, but the falx, although calcified, was not shifted. The sella was intact.A left carotid arteriogram showed an abnormal vascular pattern in the left parietal area adjacent to the skull. Ventriculography disclosed downward displacement of the lateral, superior portion of the left lateral ventricle.

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über Knorpelgeschwülste der SchÄdelbasis mit intrakranieller Ausdehnung

Cited by 29 publications

References 6 publications

Sellar chondroma in a case of Ollier's disease

Sellar chondroma in a case of Ollier's disease

Roentgenologic Findings in Chondromas of the Pontine Angle

Primary non-skeletal intracranial cartilaginous neoplasms: report of a chondroma and a mesenchymal chondrosarcoma

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