scholarly journals Abdominal wall yolk sac tumor in a child

2022 ◽  
Vol 27 (1) ◽  
pp. 94
Author(s):  
Prema Menon ◽  
Manasa Reddy ◽  
PritamSingha Roy ◽  
Shailesh Solanki ◽  
Shruti Gupta ◽  
...  
2017 ◽  
Vol 11 (1) ◽  
Author(s):  
Machiel van den Akker ◽  
Dirk Vervloessem ◽  
An Huybrechs ◽  
Sabine Declercq ◽  
Jutte van der Werff ten Bosch

1985 ◽  
Vol 134 (2) ◽  
pp. 374-376 ◽  
Author(s):  
Kazunori Kihara ◽  
Makoto Washizuka ◽  
Atsuhiko Sakamoto ◽  
Kunihiko Sakai ◽  
Nozomu Aoki ◽  
...  

Author(s):  
Manling Luo ◽  
Yuanqiao He ◽  
Baogang Xie ◽  
Shiyun Li ◽  
Fuqiang Gan ◽  
...  

Open Medicine ◽  
2021 ◽  
Vol 16 (1) ◽  
pp. 892-898
Author(s):  
Xianwen Hu ◽  
Dandan Li ◽  
Jinhua Xia ◽  
Pan Wang ◽  
Jiong Cai

Abstract Mixed germ cell tumor (MGCT) mainly occurs in young women’s ovaries and men’s testicles and rarely occurs outside the gonad. Fewer than 10 cases of mediastinal MGCT are available in PubMed, Embase, and other databases in English, while mediastinal MGCT with three pathological components, such as yolk sac tumor, immature teratoma, and embryonal carcinoma, has not been reported previously. A 12-year-old male sought medical attention for chest discomfort and underwent a computed tomography (CT) scan. A large soft tissue mass occupying most of the left thoracic cavity and mediastinum was detected. A CT-guided biopsy was performed, and an MGCT was diagnosed with pathological components, including yolk sac tumor, immature teratoma, and a small amount of embryonal carcinoma. Due to the large size of the tumor, the patient was treated with an EP regimen (etoposide + cisplatin) and paclitaxel + ifosfamide + cisplatin interstitial chemotherapy. The patient was followed up for 6 months and was alive with the disease. To the best of our knowledge, this is the 10th patient with MGCT in the mediastinum. The incidence of mediastinal MGCT is low, but it should still be considered one of the differential diagnoses of isolated pleural fibroma and neurogenic tumors.


2021 ◽  
pp. 1010-1018
Author(s):  
Marhendra Satria Utama ◽  
Andi Kurniadi ◽  
A.A. Citra Yunda Prahastiwi ◽  
Antony A. Adibrata

Yolk sac tumor (YST) is a rare malignant germ cell tumor with no appropriate treatment strategy to date. However, patients are treated on a case-to-case basis as per various case reports that have been published. Here, we present a case of 27-year-old female patient who presented to us with chief complaints of severe abdominal pain associated with leucorrhea. She previously had a similar pain episode, which was then evaluated by a multidisciplinary team. She was diagnosed with YST. After that, she underwent 6 cycles of chemotherapy, but there was no improvement. Then the medical oncologist referred her to performed radiotherapy. Then, the radiation oncologist decided to give her curative radiotherapy of 3D-CRT. After completing her sessions, she felt better and clinically improving. After that, she was discharged and scheduled a follow-up visit for first evaluation. At her follow-up visit, she was feeling well, and we decided to have an abdominal MRI.


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

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