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Biomedical subjects

G Leventon

Publications and source records attributed to G Leventon.

At least 37 records · Page 2Linked to original sources

Diagnosis of jugular paraganglioma by radionuclide angiography: concise communication.

Jugular paraganglioma is a highly vascular tumor, slowly growing, extending into the surrounding structures and causing otologic and/or neurologic symptoms according to its location in the jugular bulb region or the middle-ear. In our study, modified vertex and posterior head scintiangiography was used in seven cases. Scintiangiography was positive in all seven, whereas concomitant radiographic studies were limited: four of the seven gave positive findings by transmission computerized tomography (TCT). Only four patients underwent angiography, with positive results in two. Hypocycloidal tomography was positive in three cases. However, some radiographic studies, particularly TCT, may be useful in detecting local extension, bone destruction, and soft-tissue infiltration. Radionuclide angiography proved highly reliable and should be used initially whenever a jugular paraganglioma is suspected.

Aged↗

Human epithelial cell line established from a child with juvenile laryngeal papillomatosis.

Papillae were removed from a 2-yr-old boy with juvenile squamous cell papillomatosis and the tissue was grown in vitro. The method leading to the establishment of a continuous laryngeal papilloma cell line is described. This epithelial cell line was benign, as judged by cell morphology and cellular inability to form colonies in soft agar or to produce growing nodules in nude mice. Papilloma virus particles were not seen through the electron microscope. In the early stages of culture, the cells contained antigen that stained specifically with autologous serum.

Cell Line↗

Intracranial esthesioneuroblastoma associated with unilateral visual loss. Case report.

Esthesioneuroblastoma is a rare tumor that arises from the olfactory mucosa and presents usually as a mass in the nasal cavity. Neurological complications occur in about 20% of these cases. Nine cases have been recorded so far in which the neoplasm manifested initially as an intracranial mass. These cases are reviewed and another patient, presenting with progressive unilateral visual loss, is reported.

Adolescent↗

Malignant oncocytic tumour of the parotid salivary gland.

A 49-year-old man developed a tumour mass in his right parotid salivary gland nine years after a histologically proven benign mixed tumour of the same salivary gland had been surgically removed. Radical resection of the right parotid salivary gland and associated lymph nodes and soft tissues of the neck was performed. The parotid tumour was composed of oncocytic cells which infiltrated the surviving salivary gland tissue. Most of the excised lymph nodes contained metastatic deposits of oncocytic cells identical to the tumour seen in the parotid. There are no previous reports of the occurrence of both pleomorphic adenoma and malignant oncocytoma in the same salivary gland.

Adenoma, Pleomorphic↗