Results 181 to 190 of about 23,159 (235)
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Intracranial Choriocarcinoma

Journal of Computer Assisted Tomography, 1979
A case of intracranial choriocarcinoma (probably primary), a rare variety of atypical teratoma, is reported. Diagnosis and treatment were based on radiological and hormonal studies. The usefulness of computed tomography (CT) in the follow-up and treatment of patients with tumors in areas not easily accessible for surgical exploration or biopsy is again
C V, Rao, S, Govindan
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Intracerebral choriocarcinoma

International Journal of Gynecology & Obstetrics, 1990
Nineteen patients with gestational trophoblastic disease (GTD) metastatic to the brain are reviewed. These patients constituted 9.0% of 210 [corrected] patients with GTD treated between November 1967 and December 1987. Four patients (21%) presented with primary neurological symptoms of GTD; four patients developed brain metastases during or after ...
W B, Jones   +2 more
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Choriocarcinoma of the Thymus

JAMA: The Journal of the American Medical Association, 1962
Choriocarcinoma is a notorious, highly malignant tumor of placental or teratoid testicular origin. An obscure entity referred to as "primary extragenital chorionepithelioma of the mediastinum" is described herewith as choriocarcinoma of the thymus. The fact that this neoplasm occurs almost exclusively in young men is substantiated by similar sequences ...
P, JERNSTROM, H, McLAUGHLIN
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Choriocarcinoma of the cervix

Acta Obstetricia et Gynecologica Scandinavica, 1992
The incidence of primary cervical choriocarcinoma is extremely low, with only approximately 60 cases reported. We present a case of primary cervical choriocarcinoma, which was originally mis‐diagnosed as a cervical pregnancy. After failure of conservative treatment with methotrexate, the patient underwent a hysterectomy, followed by chemotherapy with ...
J D, Lee   +4 more
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Choriocarcinoma of the Testis

Journal of Urology, 1974
From 1960 to 1970 8 patients with metastatic choriocarcinoma of the testis were treated at the Naval Hospital in Long Beach California. The men ranged in age from 22 to 45 years. 6 patients had testicular enlargement 1 had hemoptysis and 1 had an abdominal mass. All patients were managed with chemotherapy using actinomycin D plus an aklylating agent
S C, Henry, P C, Walsh, M B, Rotner
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The diagnosis of choriocarcinoma

Clinical Radiology, 1964
Summary Choriocarcinoma, a rare malignant tumour of trophoblast, is of interest because of its favourable response to modern treatment. Diagnosis is sometimes easy, but may present problems, in part because the tumour is often haemorrhagic and necrotic, and in part because malignancy can be simulated by trophoblast itself, which is invasive and when ...
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Choriocarcinoma of the Lung

Archivos de Bronconeumología ((English Edition)), 2009
Primary choriocarcinoma of the lung is an extremely rare condition with a fatal outcome in most patients. We report the case of a 31-year-old woman with cough, chest pain, and hemoptysis, whose chest radiograph displayed nodules in the right upper lobe. After study and an unsuccessful attempt at histological characterization of the lesions, exploratory
María Elena, Corpa Rodríguez   +5 more
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The ectopic choriocarcinoma

American Journal of Obstetrics and Gynecology, 1956
Abstract 1.1. Choriocarcinoma is a very malignant and rapidly fatal tumor. 2.2. Excessive vaginal bleeding, and lesions of the vagina, lungs, and liver, especially following a recent pregnancy, should suggest the possibility of a chorionepithelioma. 3.3.
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Choriocarcinoma of the Nose

Annals of Otology, Rhinology & Laryngology, 1978
A case of choriocarcinoma in a 17-year-old unmarried female is presented. She attended the E.N.T. Clinic with a rapidly growing mass at the tip of the nose. Histologic report of the excised mass was reported as a secondary deposit from a choriocarcinoma.
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Early Development of Choriocarcinoma

American Journal of Obstetrics and Gynecology, 1966
Age. Tabulation of the ages of the patients with trophoblastic disease registered in the Albert Mathieu Chorion-epithelioma Registry is presented in Table I. The patient material is received from all parts of the United States but not all material is sent to the Registry. None has been sent on the basis of the age of the patient.
J I, Brewer, A B, Gerbie
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