scholarly journals Ovarian Carcinosarcoma with Yolk Sac Tumor in a Post-Menopausal Female: A Case Report and Review of Literature

2021 ◽  
Vol 6 (2) ◽  
pp. 59-65
Author(s):  
Margarita Rae Rosario ◽  
◽  
Jeffrey So ◽  
Claire Anne Therese Hemedez ◽  
Carlos Dy
2021 ◽  
pp. 100748
Author(s):  
Risha Sinha ◽  
Bethany Bustamante ◽  
Alexander Truskinovsky ◽  
Gary L. Goldberg ◽  
Karin K. Shih

2016 ◽  
Vol 2 (1) ◽  
pp. 15-17
Author(s):  
A Sreehari ◽  
BM Rupakala

ABSTRACT A total of 3 to 5% of all ovarian malignancies include malignant ovarian germ cell tumors (MOGCTs). They are subdivided into germinomatous and non-germinomatous tumors. Common types of non-germinomatous tumors include yolk sac and immature teratoma. Ovarian yolk sac tumors (YST) are the second most frequent histological subtype of MOGCTs, after ovarian dysgerminoma. They account for 20% of MOGCTs and are frequent especially in childhood and in early adulthood. We report the case of a yolk sac tumor of the ovary in a 13yrs years old female. How to cite this article Sreehari A, Rupakala BM, Sarojamma C. Ovarian Yolk Sac Tumor: A Case Report with Review of Literature. J Med Sci 2016;2(1):15-17.


2013 ◽  
Vol 18 (2) ◽  
pp. 86 ◽  
Author(s):  
Prema Menon ◽  
Richa Jain ◽  
Ashim Das ◽  
ToijamSoni Lyngdoh

2018 ◽  
Vol 23 (4) ◽  
pp. 232 ◽  
Author(s):  
Ankur Mandelia ◽  
Nijagal Mutt ◽  
Richa Lal ◽  
Raghunandan Prasad

2005 ◽  
Vol 35 (1) ◽  
pp. 077-082 ◽  
Author(s):  
Masashi Kanai ◽  
Ayao Torii ◽  
Akihiko Hamada ◽  
Yoko Endo ◽  
Yasuhiro Takeda ◽  
...  

2020 ◽  
Author(s):  
Yuting Zhang ◽  
Lusheng Li ◽  
Ling He

Abstract Background: Yolk sac tumor also known as endodermal sinus tumor, is a rare intracranial germ cell tumor. We reported a case of yolk sac tumor in cerebellar hemisphere, and reviewed associated literatures. The majority of tumor locations are near the midline. On review of literature, very few case reports of intracranial yolk sac tumor have been published, and there is only one case report has described a yolk sac tumor arising from the cerebellum. Case presentation: A two years old boy admitted to our hospital due to headache and unsteady gait for six days. CT and MRI demonstrated a tumor in the right cerebellar hemisphere, and the blood and cerebrospinal fluid alpha-fetoprotein were found increased. It was diagnosed as yolk sac tumor after operation comfirmed by histopathological examination. Postoperative chemotherapy was performed, and the patient suffered no tumor recurrence one year and a half after the surgery. Conclusions: The clinical characteristics and imaging diagnosis of intracranial yolk sac tumor are lack of specificity, the comfirmed diagnosis is depending on the combination of elevated alpha-fetoprotein and histopathological examination.


Author(s):  
Burak Hazir ◽  
Berkay Şímșek ◽  
Arzu Erdemír ◽  
Fatih Gürler ◽  
Ozan Yazici ◽  
...  

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