Zobrazeno 1 - 10
of 2 275
pro vyhledávání: '"yolk sac tumor"'
Publikováno v:
BMC Women's Health, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Yolk sac tumor (YST) is a highly malignant germ cell tumor, a majority of which originate from the gonads and are extremely rare from endometrium. Case presentation Here we present a case of a 42-year-old woman suffered from prima
Externí odkaz:
https://doaj.org/article/322bbee126d9467481a8062198c20ba1
Autor:
Sara Ez-zaky, MD, Salma Marrakchi, MD, Sara Essetti, MD, Sanae Jellal, MD, Najat Lamalmi, PhD, Nazik Allali, PhD, Latifa Chat, PhD, Siham El Haddad, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 5872-5876 (2024)
Yolk sac tumors can occur in various extragonadal sites, including the hepatobiliary tract, and are often associated with elevated serum alpha-fetoprotein. We report the case of a 14-month-old male infant presenting with abdominal pain and distension
Externí odkaz:
https://doaj.org/article/e6238fd6425641ef94d4cd3705eea5b9
Autor:
Tom Vandaele, Jan Van Slambrouck, Patrick Schöffski, Herlinde Dumez, Birgit Weynand, Raf Sciot, Annalisa Barbarossa, An-Lies Provoost, Kristof Van de Voorde, Yves Debaveye, Sofian Bouneb, Philippe Nafteux, Laurens J. Ceulemans
Publikováno v:
World Journal of Surgical Oncology, Vol 22, Iss 1, Pp 1-12 (2024)
Abstract Background Pleural neoplasms are rare and can be subdivided into pleural metastasis and primary pleural neoplasms. Non-mesothelioma primary pleural neoplasms are a diverse group of extremely rare pathologies. Case presentation In this case s
Externí odkaz:
https://doaj.org/article/3b9699ca8efa44beb4a7a5afbe584a46
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
The manifestation of a giant ovarian yolk sac tumor during late pregnancy is relatively rare. A yolk sac tumor is a highly malignant germ cell tumor that originates from primitive germ cells. It is characterized by yolk sac differentiation in vitro.
Externí odkaz:
https://doaj.org/article/ff7fa3d24f87413e8839616e18049f64
Publikováno v:
Gynecological Endocrinology, Vol 40, Iss 1 (2024)
Ovarian steroid cell tumor, not otherwise specified (SCT-NOS), is a rare subtype of sex cord-stromal tumor, characterized by hirsutism and virilization. There are, however, few tumor markers reported in the tumor. The following is a case report. Six
Externí odkaz:
https://doaj.org/article/91e55acd3f8f4605938b91fe43832e93
Akademický článek
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Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
ObjectivesYolk sac tumors (YSTs) are rare and highly malignant ovarian malignancies that have a very poor prognosis. The aim of this study is to delineate the ultrasound and clinicopathological features of female pelvic YSTs to better understand the
Externí odkaz:
https://doaj.org/article/1bfb2e25ca0f4bbb84972d2526d3ce0d
Autor:
Junfeng Zhao, Le Qin, Guorong He, Tiancheng Xie, Guanghui Hu, Furan Wang, Hongji Zhong, Jianming Zhu, Yunfei Xu
Publikováno v:
Cancer Medicine, Vol 12, Iss 23, Pp 21293-21307 (2023)
Abstract Background Glypican‐3 (GPC3) is highly expressed in testicular yolk sac tumor (TYST). GPC3 has been evaluated as a cancer vaccine for some types of tumors, but little is known on the effects of GPC3 peptide‐based therapy on TYST. Here, w
Externí odkaz:
https://doaj.org/article/9efd101904634348ba6ee0be4f57dc81
Publikováno v:
Frontiers in Oncology, Vol 13 (2024)
Ovarian mature teratoma represents a benign ovarian tumor, while ovarian yolk sac tumor (YST, endodermal sinus tumor) is a rare malignant tumor predominantly affecting young women, often associated with a grim prognosis post-metastasis. Both ovarian
Externí odkaz:
https://doaj.org/article/4189f153dbd640128d536ac91cff3927
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
The occurrence of synchronous bilateral testicular germ cell tumors (BTGCTs) of different pathologic histologic types in pediatric patients is rare. We reported a case of a left testicular yolk sac tumor (YST) combined with a right testicular mature
Externí odkaz:
https://doaj.org/article/c843f92e7521421c87e9989e92e9731c