Zobrazeno 1 - 10
of 506
pro vyhledávání: '"Growing teratoma syndrome"'
Autor:
Daiken Satake, Manabu Natsumeda, Kaishi Satomi, Mari Tada, Taro Sato, Noritaka Okubo, Keita Kawabe, Haruhiko Takahashi, Yoshihiro Tsukamoto, Masayasu Okada, Masakazu Sano, Haruko Iwabuchi, Nao Shibata, Masaru Imamura, Chihaya Imai, Hirokazu Takami, Koichi Ichimura, Ryo Nishikawa, Hajime Umezu, Akiyoshi Kakita, Makoto Oishi
Publikováno v:
Current Oncology, Vol 31, Iss 4, Pp 1831-1838 (2024)
Molecular analysis of the growing teratoma syndrome has not been extensively studied. Here, we report a 14-year-old boy with a growing mass during treatment for a mixed germ cell tumor of the pineal region. Tumor markers were negative; thus, growing
Externí odkaz:
https://doaj.org/article/0da2ebd7e2c04fa6ba30f6615b16a2c8
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Growing teratoma syndrome (GTS) is a rare condition that arises secondary to malignant germ cell tumors. It is characterized by an enlarging abdominal mass during or after chemotherapy, normal tumor markers, and histopathological indications of matur
Externí odkaz:
https://doaj.org/article/00bead00bbba4166952e2bd9bb6373c8
Autor:
Sosho Kajiwara, Hideo Nakamura, Kiyohiko Sakata, Satoru Komaki, Tetsuya Negoto, Motohiro Morioka
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract Background Primary central nervous system (CNS) germ cell tumors (GCTs) are rare neoplasms predominantly observed in the pediatric and young adult populations. A mixed GCT including immature teratoma exhibiting growing teratoma syndrome is p
Externí odkaz:
https://doaj.org/article/b5ce55ddfd4f4920b3a0e5f7056d9a2b
Publikováno v:
Diagnostic Pathology, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background Primary liver immature teratoma is extremely rare and only 4 cases have been reported, let alone with growing teratoma syndrome (GTS) and/or gliomatosis peritonei (GP). Case presentation Here, we report a case of a 44-year-old fem
Externí odkaz:
https://doaj.org/article/7362f8a2e6eb4bfe8fc726d882c776fa
Publikováno v:
Current Oncology, Vol 29, Iss 9, Pp 6364-6372 (2022)
Coexistent growing teratoma syndrome (GTS) and gliomatosis peritonei (GP) arising during chemotherapy of ovarian immature teratoma (IMT) is extremely rare and can be misdiagnosed as recurrent or progressive disease. We present a 33-year-old woman dia
Externí odkaz:
https://doaj.org/article/3747fe64deee4caf9b706260767e4205
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 32, Iss 03, Pp 301-307 (2022)
Context Growing teratoma syndrome (GTS) is a rare entity seen following chemotherapy for metastatic nonseminomatous germ cell tumors, characterized by increase in size of the metastatic deposits, with normal serum tumor markers. Aims In this article,
Externí odkaz:
https://doaj.org/article/02bba36c37554d1daf7ac02947f27dbd
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Current Oncology, Vol 29, Iss 6, Pp 4148-4154 (2022)
Growing teratoma syndrome (GTS) is rare and can mimic disease recurrence in patients with a history of immature teratoma. Benign hypermetabolic lymphadenopathy found on staging and surveillance computed tomography (CT) and positron emission tomograph
Externí odkaz:
https://doaj.org/article/fa2bac93f17c445faf552858e59c7e42
Autor:
Miho Iwai, Kaori Yoriki, Kohei Aoyama, Yosuke Tarumi, Hisashi Kataoka, Tetsuya Kokabu, Toshiaki Numajiri, Taisuke Mori
Publikováno v:
Gynecologic Oncology Reports, Vol 46, Iss , Pp 101161- (2023)
While cancer cure is the primary goal, fertility preservation is also a cornerstone of the underlying principle of treatment for ovarian germ cell tumors. Growing teratoma syndrome (GTS) presents with growth of mature teratomas during or after chemot
Externí odkaz:
https://doaj.org/article/2dd7df4206364d2ead1faba0fdbcf8b1