Results 201 to 210 of about 16,798 (239)

Full-Thickness Eye Wall Resection of Choroidal Neoplasms

Ophthalmology, 1979
Sclerochorioretinal (full-thickness eye wall) resection was performed in 19 eyes with choroidal neoplasms. Thirteen of these eyes have retained useful vision, ranging from 20/25 to counting fingers. Six eyes had intraoperative and postoperative complications that have led to enucleation.
G A, Peyman, M, Raichand
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Childhood choroid plexus neoplasms

European Journal of Pediatrics, 1983
Fourteen children less than 2 years old with choroid plexus papilloma (CPP) were studied. Of these patients nine had the tumor in the lateral ventricles (LV), three in the fourth ventricle (4th V), one in the third ventricle (3rd V) and one in the third and left lateral ventricle (LLV).
I, Pascual-Castroviejo, F, Villarejo, A, Perez-Higueras, C, Morales, S I, Pascual-Pascual   +4 more
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Ultrasonic diagnosis of a choroid plexus neoplasm in a child

The British Journal of Radiology, 1984
Choroid plexus neoplasms arise from the epithelial cells of the choroid plexus of the brain and can occur wherever choroid plexus is found within the cranial cavity. Although relatively uncommon, these tumours are usually benign and are often accessible to surgical removal. It is therefore of paramount importance that their presence be recognised early
P S, Reddy, S R, Wild, G M, Hendry
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Pediatric choroid plexus neoplasms: MR, CT, and pathologic correlation.

Radiology, 1989
Choroid plexus papillomas are rare, constituting approximately 0.5% of all intracranial neoplasms. Four benign choroid plexus papillomas and one choroid plexus carcinoma were retrospectively reviewed in patients aged 4-20 months who had been examined with magnetic resonance (MR) imaging with a field strength of 0.5 T or 1.0 T and with computed ...
T L, Coates, D B, Hinshaw, N, Peckman, J R, Thompson, A N, Hasso, B A, Holshouser, D S, Knierim   +6 more
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NEOPLASM OF THE CHOROID PLEXUS

American Journal of Diseases of Children, 1934
Neoplasms of the brain in infancy undoubtedly occur with greater frequency than reports of their discovery would suggest. Because of the readiness with which their symptomatology may be confused with that of gastro-intestinal dysfunction, particularly projectile vomiting, uncomplicated by a lesion of the nervous system, recognition of the presence of ...
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The Role of Radiotherapy in the Management of Choroid Plexus Neoplasms

Tumori Journal, 1989
Choroid plexus papillomas are very rarely reported neoplasms in both the surgical and radiological literature. The authors present their series of 7 papillomas and 1 carcinoma. They review the recent and former literature with the aim of demonstrating the role and usefulness of radiotherapy.
M, Palazzi, A, Di Marco, F, Campostrini, A, Grandinetti, L, Bontempini   +4 more
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A marker for primary choroid plexus neoplasms.

The American journal of pathology, 1990
Primary choroid plexus (CP) tumors are rare neoplasms that present in childhood or, less frequently, in adult life. The majority are benign and amenable to complete surgical excision, but occasionally more invasive variants are encountered. Although generally pathologically distinct, occasionally primary CP neoplasms may be difficult to distinguish ...
J, Herbert, T, Cavallaro, A J, Dwork
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Differential diagnosis of choroidal neoplasms.

Oncology (Williston Park, N.Y.), 1991
Experienced ophthalmologists who appropriately employ ancillary diagnostic testing, including fluorescein angiography, ocular ultrasonography, MRI, and fine needle aspiration biopsy, are remarkably accurate in the diagnosis of intraocular neoplasms. Recognizing the classic clinical features of the more commonly encountered lesions, such as choroidal ...
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Transthyretin immunoreactivity in choroid plexus neoplasms and brain metastases.

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 1992
Although choroid plexus papillomas (CPP) and primary choroid plexus carcinomas (CPC) are rare neoplasms of the central nervous system, they have been the subject of a number of immunohistochemical studies. To date, no unique or specific marker for these neoplasms has been found, however.
S, Albrecht, E, Rouah, L E, Becker, J, Bruner   +3 more
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[Choroid metastasis consequence of breast neoplasm].

Oftalmologia (Bucharest, Romania : 1990), 2004
The paper presents a clinical case of a 46 years old woman with metastatic carcinoma the leading point being breast and the therapeutical modalities taken in this situation.
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