Results 21 to 30 of about 30,169 (198)

Yolk sac tumor of cryptorchid testis diagnosed by fine needle aspiration cytology

Journal of Cytology, 2015
Yolk sac tumor is the most common germ cell tumor in infants and children. Majority of them arise in the gonads. Yolk sac tumor of undescended testis has been rarely diagnosed.
Monisha Choudhury, Shivali Sehgal, Anita Nangia, Rajiv Chadha   +3 more
doaj   +1 more source

PRDM14 is expressed in germ cell tumors with constitutive overexpression altering human germline differentiation and proliferation. [PDF]

, 2018
Germ cell tumors (GCTs) are a heterogeneous group of tumors occurring in gonadal and extragonadal locations. GCTs are hypothesized to arise from primordial germ cells (PGCs), which fail to differentiate.
Chen, Di, Clark, Amander T, Gell, Joanna J, Hunt, Timothy J, Zhao, Jasmine   +4 more
core   +2 more sources

Ovarian Carcinosarcoma with Yolk Sac Tumor in a Post-Menopausal Female

Philippine Journal of Pathology, 2021
Yolk sac tumor is the second most common subtype of ovarian germ cell tumors and is rare in postmenopausal women. The few cases in literature have found that in this age group, yolk sac tumors more commonly present as a mixed component, combined with ...
Margarita Rae Rosario, Jeffrey So, Claire Anne Therese Hemedez, Carlos Dy   +3 more
doaj   +1 more source

Management of Ovarian Yolk Sac Tumor in Pregnancy in a Limited Resource Setting: Case Report [PDF]

Middle East Journal of Cancer, 2021
Ovarian yolk sac tumor in pregnancy is a very rare case (
Tofan Utami, Herdhana Suwartono, Erda Umami, Anggara Mahardika, Raymond Surya, Laila Nurana   +5 more
doaj   +1 more source

Management of germ cell tumors in children: Approaches to cure [PDF]

, 2002
The introduction of cisplatinum chemotherapy and current advances in the surgical treatment have resulted in a dramatic improvement of the prognosis of children with malignant germ cell tumors (GCT).
Calaminus, G., Göbel, U., Haas, R. J., Schmidt, P., Schneider, D. T.   +4 more
core   +1 more source

Extraovarian pelvic yolk sac tumors [PDF]

Cancer, 1988
The clinical and pathologic features of four extraovarian pelvic yolk sac tumors (YST) are described. The women, 17 to 39 years of age, were found to have a pelvic mass on physical examination, or in one case, at cesarean section. The tumors were bulky and arose within, or in close proximity to, the uterus. One tumor involved the endometrial cavity and
P B, Clement, R H, Young, R E, Scully
openaire   +2 more sources

A rare case of primary mediastinal yolk sac tumor

Archives of Medicine and Health Sciences, 2014
Yolk sac tumor (endodermal sinus tumor) is a subtype of germ cell tumor and a highly malignant neoplasm. In addition to presenting in ovaries and testes, the tumor has been detected at several extragonadal sites, including the presacral area, the ...
Vinay Mahishale, Prakash R. Malur, Virupakshi Hattiholi, Sindhuri Avuthu, Ankit Rathi   +4 more
doaj   +1 more source

Tumor Mediastinum Anterior (Yolk Sac Tumor) pada Seorang Laki-Laki Dewasa Muda: Sebuah Kasus yang Jarang [Yolk Sac Tumor in a Young Man: A Rare Case]

Jurnal Respirasi, 2016
Background: Primary mediastinal yolk sac tumor is an extremely rare and highly malignant tumors occuring in children and young adult. They are more common in men.
Risnawati Risnawati, Laksmi Wulandari
doaj   +1 more source

Primary yolk sac tumor of seminal vesicle: a case report and literature review

World Journal of Surgical Oncology, 2012
Background Yolk sac tumor (endodermal sinus tumor) is a rare malignant germ cell tumor arising in the testis or ovary. Extragonadal yolk sac tumor is even rarer and has only been described in case reports.
Yao Xu-Dong, Hong Ya-Ping, Ye Ding-Wei, Wang Chao-Fu   +3 more
doaj   +1 more source

The complex TIE between macrophages and angiogenesis [PDF]

, 2020
Macrophages are primarily known as phagocytic immune cells, but they also play a role in diverse processes, such as morphogenesis, homeostasis and regeneration.
Anghelina M., Avraham‐Davidi I., Baer C., Bailey A. S., Barnett F. H., Bonnardel J., Chakarov S., Chen L., Coffelt S. B., Corliss B. A., Cursiefen C., Daly C., Davies L. C., Davies L. C., De Palma M., De Palma M., De Palma M., De Palma M., De Palma M., De Spiegelaere W., DeFalco T., Deshmane S. L., Detry B., Dimova I., Dimova I., Eklund L., Elamaa H., Eubank T. D., Fantin A., Ferrari G., Fukuhara S., Ganta V. C., Ganta V. C., García S., Gerri C., Grunewald M., Guo L., Gurevich D. B., Hamm A., Hazan A. D., He H., Hoeffel G., Itoh M., Jetten N., Kim M., Kochhan E., Korhonen E. A., Korpelainen E. I., Krishnasamy K., Kumar A. H., Leibovich S. J., Lim H. Y., Liu C., Lucas T., Master Z., Metharom P., Michaeli S., Moldovan N. I., Moore E. M., Mueller S. B., Murdoch C., Murray P. J., Patel A. S., Polverini P. J., Potente M., Pucci F., Saharinen P., Saharinen P., Schif‐Zuck S., Schmeisser A., Seaman S. A., Seok S. H., Spiller K. L., Venneri M. A., Vestweber D., Webster N. L., West M. E. D., Willenborg S., Yamamoto S., Zajac E., Zenker D., Zhang W.   +81 more
core   +2 more sources