Results 171 to 180 of about 1,321,937 (219)
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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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Pure Yolk-Sac Tumor of the Lung
Asian Cardiovascular and Thoracic Annals, 2008Primary germ cell tumors of the chest often localize in the anterior mediastinal compartment. Such tumors originating from lungs and pleura are rare. Chest tomography revealed a mass in the middle lobe of the right lung in a 25-year-old man. A middle lobe medial segmentectomy was performed, and chemotherapy was applied postoperatively.
Basoglu A. +4 more
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Visceral yolk sac-derived tumors
The International Journal of Developmental Biology, 1993Externalization of the visceral yolk sac, after fetectomy, induces the development of extra-embryonal fetal tumors in rodents. These tumors are either benign teratomas that appear 3 to 4 weeks after the displacement of the yolk sac or malignant tumors, i.e. yolk sac carcinomas. The latter appear 4 to 8 months after the surgery.
H, Sobis, A, Verstuyf, M, Vandeputte
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Primary Yolk Sac Tumor of the Lung
The Annals of Thoracic Surgery, 2009Yolk-sac tumor mimics the yolk sac of the embryo, and the presence of alpha fetoprotein in the tumor cells is highly characteristic. We present an 18-year-old boy with primary pulmonary yolk-sac tumor diagnosed postoperatively. A computed tomographic scan revealed a huge intrathoracic soft tissue mass 20 x 25 cm occupying most of the left hemithorax ...
Abdel Rahman M, Abdel Rahman +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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Pure Yolk-Sac Tumor of the Lung
The Thoracic and Cardiovascular Surgeon, 1993The first case of a pure primary yolk-sac tumor of the lung is presented. The tumor developed in the right upper lobe of a 31-year-old man; preoperatively, the serum alpha-fetoprotein concentration was elevated. Treatment consisted of pulmonary segmentectomy with postoperative combination chemotherapy.
H, Inoue +6 more
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Krukenberg Tumor With Yolk Sac Tumor Differentiation
International Journal of Gynecological Pathology, 2008An unusual case of bilateral Krukenberg tumor with foci of yolk sac tumor (YST) differentiation occurring in a 50-year-old patient is reported. The primary tumor was in the gastric antrum, and it showed morphology of poorly differentiated adenocarcinoma with diffuse and solid growth pattern.
Michal, Zamecnik +3 more
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An Intraocular Yolk Sac Tumor in a Child
Optometry and Vision Science, 2013ABSTRACT Purpose To report a case of intraocular yolk sac tumor (YST) misdiagnosed as retinoblastoma (RB) by several hospitals. Case Report A 2‐year‐old girl presented to our hospital because of swelling and pain of ...
Chenyang, Cong +4 more
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Primary yolk sac tumor of the endometrium
International Journal of Gynecology & Obstetrics, 2011[1] Van Calster B, Timmerman D, Bourne T, Testa AC, Van Holsbeke C, Domali E, et al. Discrimination between benign and malignant adnexal masses by specialist ultrasound examination versus serum CA-125. J Natl Cancer Inst 2007;99(22): 1706–14. [2] Valentin L, Jurkovic D, Van Calster B, Testa A, Van Holsbeke C, Bourne T, et al.
Changyu, Wang +4 more
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Yolk sac tumor in the nasal cavity
American Journal of Otolaryngology, 2008Yolk sac carcinoma (YST) is rare malignant tumor of germ cell origin. It most commonly arises from the gonads but extragonadal sites of origin are reported in 20% of the cases. Head and neck germ cell tumors are uncommon and only a small number are malignant. We present the case of a 48 years old man presenting with a YST of the sinonasal tract and the
Bernardo Cunha Araujo, Filho +3 more
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