Results 11 to 20 of about 5,721 (211)

Extragonadal Mixed Germ Cell Tumour of the Right Scapular Region: A Case Report [PDF]

Journal of Nepal Medical Association, 2022
Extragonadal germ cell tumours are rare; to the best of our knowledge, a location in the soft tissue of the right scapular region has never been previously reported in the literature.
Sushma Gurung, Sabina Karim, Sagun Thapa, Shristi Gautam   +3 more
doaj   +2 more sources

Testicular seminoma after the complete remission of extragonadal yolk sac tumor : a case report

BMC Urology, 2004
Background Between 2% and 5% of malignant germ-cell tumors in men arise at extragonadal sites. Of extragonadal germ cell tumors, testicular carcinoma in situ (CIS) are present in 31–42% of cases, and CIS are reported to have low sensitivity to ...
Yanaihara Hitoshi, Nakagawa Ken, Mitsuhashi Tomoko, Ueno Munehisa, Kuroda Isao, Tsukamoto Takuji, Deguchi Nobuhiro   +6 more
doaj   +2 more sources

Parasitic mature cystic ovarian teratoma: A rare case of autoimplantation of a twisted dermoid cyst

Clinical Case Reports, 2023
Key Clinical Message Extragonadal parasitic dermoid cysts are rare. Diagnosis of such extragonadal parasitic teratoma is often done intraoperatively during surgical exploration of abdominal mass.
Suraj Shrestha, Sugat Adhikari, Chandra Narayan Yadav, Elisha Poddar, Shekhar Bhatta, Surendra Sapkota, Ramesh Khadayat, Garima Neupane, Simin Kunwar, Pradeep Raj Regmi   +9 more
doaj   +2 more sources

Atypical extragonadal germ cell tumors

Journal of Indian Association of Pediatric Surgeons, 2012
Aim: To review the experience with the diagnosis and management of extragonadal germ cell tumors (GCT) with a subset analysis of those with atypical features.
Mainak Deb, Suravi Mohanty, Anuradha Ananthamurthy, Isha Garg, Kanishka Das   +4 more
doaj   +2 more sources

Klinefelter Syndrome with Poor Risk Extragonadal Germ Cell Tumor

Urology Case Reports, 2017
Germ cell tumors are the most common malignancy in men aged 15-35 years old, with a small percentage presenting in an extragonadal location. These tumors are seldom identified in the gastrointestinal tract.
Jeremy A. Konheim, Jonathan A. Israel, Scott E. Delacroix   +2 more
doaj   +2 more sources

Primary Extragonadal Germ Cell Tumors in Klinefelter Syndrome: 10-Years of Experience from a Single Institute [PDF]

Clinical Pediatric Hematology-Oncology, 2020
Background : : Approximately 8% of male patients presenting with primary mediastinal germ cell tumors (GCTs) have Klinefelter syndrome (KS), while patients diagnosed with retroperitoneal GCTs also exhibit a range of chromosomal abnormalities.
Yura Kim, Won Kee Ahn, Jung Woo Han, Seung Min Hahn, Seung Yeon Kwon, Chuhl Joo Lyu   +5 more
doaj   +2 more sources

A rare case of extragonadal mixed germ cell tumor of the Sacrococcygeal Region with mature thymic tissue in the teratoma component

Journal of Indian Association of Pediatric Surgeons, 2023
A rare extragonadal mixed germ cell tumor of the sacrococcygeal area presenting with mature thymic tissue in the teratomatous component, a rare finding and the first reported case of such an association.
Anubhuti Chaturvedi, Reena Tomar, Kirti Balhara, Nita Khurana, Simmi K Ratan, Aparajita Mitra   +5 more
doaj   +2 more sources

Mullerian adenosarcoma-like tumor arising from an extragonadal germ cell tumor: Case Report and Literature Review [PDF]

Human Pathology Reports
Extragonadal germ cell tumors (GCTs) are rare neoplasms, accounting for 1–5 % of all germ cell tumors. Mixed germ cell tumors are neoplasms with more than one GCT component.
Pauline Biesemans, Marcella Baldewijns, Steven Joniau, Tim Van Assche, Marc Claessens, Robert Hente, Wies Vanderbruggen, Wim Volders, Anne-Sophie Van Rompuy   +8 more
doaj   +2 more sources

Extragonadal mixed germ cell tumor of the right arm: description of the first case in the literature [PDF]

World Journal of Surgical Oncology, 2012
Background Extragonadal localization of germ cell tumors (GCTs) is rare; to the best of our knowledge, a location in the soft tissue of the arm has never been previously reported in the literature.
Benali Hicham, Lalya lssam, Allaoui Mohamed, Benmansour Aniss, Elkhanoussi Basma, Benjelloun Samir, Benjaafar Noureddine, Elyaacoubi Mourad   +7 more
doaj   +2 more sources

Successful Treatment of Primary Mediastinal Seminoma With Radiotherapy Following Chemotherapy Under a Bloodless Treatment Policy Based on Patient's Religious Sentiments. [PDF]

IJU Case Rep
ABSTRACT Introduction Primary mediastinal seminoma is rare with a favorable prognosis when appropriately treated, and surgical resection after chemotherapy is the standard treatment. However, refusal of blood transfusion for religious reasons can limit curative surgical management. Case Presentation A 47‐year‐old Jehovah's Witness man was found to have
Fujii E, Yamamoto Y, Takezawa K, Hatano K, Kakuta Y, Kawashima A, Nonomura N, Kato T.   +7 more
europepmc   +2 more sources