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Extensive surgical resections for rare pleural neoplasms: a single-center experience with a yolk sac tumor and synovial sarcoma. [PDF]
Vandaele T +12 more
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Cell elongation is key to in silico replication of in vitro vasculogenesis and subsequent remodeling [PDF]
BRODSKY, SV +4 more
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International Journal of Gynecological Cancer, 2021
Ovarian germ cell tumors derive from ovarian germ cells and account for approximately 20% of all ovarian neoplasms. Only 1–2% of ovarian germ cell tumors are called malignant ovarian germ cell tumors and constitute approximately 3–5% of all malignant ovarian neoplasms.[1][1] Yolk sac ...
Teresa Iscar +3 more
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Ovarian germ cell tumors derive from ovarian germ cells and account for approximately 20% of all ovarian neoplasms. Only 1–2% of ovarian germ cell tumors are called malignant ovarian germ cell tumors and constitute approximately 3–5% of all malignant ovarian neoplasms.[1][1] Yolk sac ...
Teresa Iscar +3 more
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Archenteronoma (yolk sac tumors)
Journal of Pediatric Surgery, 1978Ten cases of archenteronoma are reviewed with a follow-up between 2 mo and 7 yr. Their presentation was similar to that of rhabdomyosarcoma except for testicular tumors that may present as a hydrocele. A good prognosis was found with tumors amenable to primary resection and chemotherapy.
A E, Mackinnon, S J, Cohen
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The Spine Journal, 2016
A1-year-old infant presented to our hospital with a pelvic mass. There was no history of surgery, and the clinical examination revealed a pelvic palpable lesion. Magnetic resonance imaging showed a pelvic mass that was heterogeneous on T1-weighted and T2-weighted images, and it was heterogeneously enhanced after contrast administration (Fig.
POLAT, Gökhan +4 more
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A1-year-old infant presented to our hospital with a pelvic mass. There was no history of surgery, and the clinical examination revealed a pelvic palpable lesion. Magnetic resonance imaging showed a pelvic mass that was heterogeneous on T1-weighted and T2-weighted images, and it was heterogeneously enhanced after contrast administration (Fig.
POLAT, Gökhan +4 more
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Primary Intracardiac Yolk Sac Tumor
Pediatric Cardiology, 1998A 2-year-old male child presented with fever, complete heart block, and congestive cardiac failure. Echocardiography showed a dumbbell-shaped mass in the right ventricle and right atrium. He was operated on with a provisional diagnosis of rhabdomyoma.
U, Parvathy +4 more
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Cytodiagnosis of yolk sac tumor
The Indian Journal of Pediatrics, 2004To analyze cytomorphologic features of yolk sac tumors of childhood. Four cases of pediatric yolk sac tumor (YST), diagnosed by fine needle aspiration cytology were reviewed (1998-2002). Age of patients ranged from 1(1/2) to 5 years. Three cases presented clinically with an intra-abdominal mass while one case presented with a testicular mass.
Nishat, Afroz, Nazoora, Khan, R S, Chana
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Intracardiac yolk sac tumor: Echocardiographic evaluation
Pediatric Cardiology, 1996To our knowledge, this case of an abdominal yolk sac tumor with extensive cardiac involvement is the first to be reported in a pediatric patient. The report describes the echocardiographic findings of the tumor and the role of echocardiography in providing important information for patient management decisions.
C G, Cowley +4 more
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Pathology Case Reviews, 2006
Abstract: Ovarian yolk sac tumors are malignant germ cell tumors of young women that exhibit a range of histologic growth patterns that may mimic several other primary and secondary ovarian tumors. Reticular, endodermal sinus, polyvesicular-vitelline, hepatoid, and glandular architectures represent the chief morphologic patterns.
Joseph T. Rabban, Charles Zaloudek
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Abstract: Ovarian yolk sac tumors are malignant germ cell tumors of young women that exhibit a range of histologic growth patterns that may mimic several other primary and secondary ovarian tumors. Reticular, endodermal sinus, polyvesicular-vitelline, hepatoid, and glandular architectures represent the chief morphologic patterns.
Joseph T. Rabban, Charles Zaloudek
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