منابع مشابه
Congenital Malignant Neurilemmoma.
A unique case of a congenital malignant neurilemmoma in a newborn baby is described.
متن کاملSolitary orbital malignant neurilemmoma.
A SERIES of 500 cases of proptosis included two due to orbital malignant neurilemmoma, which according to Duke-Elder (1952) and Hogan and Zimmerman (1962) is a very rare condition. Case Reports Case 1, a 50-year-old woman (Fig. 1), had a left forward painless proptosis of 7-months' duration. Examination.-The right eye was normal and the visual acuity 6/9. The left eye showed proptosis 23 mm. (r...
متن کاملMalignant neurilemmoma of left atrium.
A 31-year-old woman, whose chief complaint was back pain, was found to have an echocardiographic abnormality suggestive of a left atrial myxoma. Angiography clearly showed a large radiolucent mass protruding from the left atrium into the left ventricle during diastole. X-rays of the sacrum disclosed the presence of a malignant tumour. Biopsy specimens taken from the tumour in the sacral plexus ...
متن کاملAnterior uveal neurilemmoma--a rare neoplasm simulating malignant melanoma.
A 30-year-old woman presented with dilated episcleral vessels in the right eye which were found to be associated with an underlying ciliary body tumour. Contact lens examination, transpupillary transillumination, ultrasonography, computerised tomography, magnetic resonance imaging, and fine needle aspiration biopsy produced apparently conflicting and inconclusive results, and the eye was enucle...
متن کاملCongenital malignant gliosarcoma.
Malignant gliosarcoma is an extremely rare, anaplastic tumor which to date has been found exclusively in adults. This type of sarcoma is a form of mixed glioma and sarcoma which is quite different and distinct from the type of sarcoma that arises in a glioblastoma [1]. Less than 10 cases of this entity have been reported [2-5]. We report a case of this unusual tumor in a 4-month-old girl who ha...
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ژورنال
عنوان ژورنال: Journal of Clinical Pathology
سال: 1964
ISSN: 0021-9746
DOI: 10.1136/jcp.17.2.130