A CASE OF SPONTANEOUSLY RUPTURED PRIMARY URACHAL YOLK SAC TUMOR
نویسندگان
چکیده
منابع مشابه
Primary omental yolk sac tumor
Extra-ovarian yolk sac tumor arising in the omentum is extremely rare. As yolk sac tumor originated from the omentum has been rarely reported, its clinical information is very limited. The authors encountered a case of yolk sac tumor originated from the omentum, and reported the case herein. A 32-year-old woman was presented with developed low abdominal distension for a month. Magnetic resonanc...
متن کاملPrimary Yolk Sac Tumor of Omentum: a Case Report
Yolk sac tumor (YST) is one of the rare malignant germ cell tumor and usually occurs in gonad. Extragondal sites of YSTs are reported in mediastinum, vagina, brain, and retroperitoneum but are extremely rarely in omentum. The clinicopathologic feature of primary omental YST is not well known and there are only 5 cases reported currently. Recently we experienced a primary YST of omentum in 27-ye...
متن کاملYOLK SAC TUMOR OF VAGINA
Malignant germ-cell tumors (MGCT) are rare tumors of childhood accounting for less than 3% of pediatric malignancies. Endodermal sinus tumor (EST) forms the most common histologic subtype of MGCT. The vagina is an extremely rare site for GCTs. An 8-month-old female was admitted with a short history of vaginal bleeding, and a mass protruding from the vagina. She was pale and a mass was palpab...
متن کاملPrimary Hepatic Yolk Sac Tumor: A Case Report of a Ruptured Tumor in a 22-month-old Boy
Primary hepatic yolk sac tumor is a rare extra-gonadal germ cell tumor in children and adults. Two important differential diagnoses for hepatic tumor in a pediatric patient are hepatocellular carcinoma and hepatoblastoma. A 22-month-old boy presented to our hospital with acute respiratory distress and increased serum alphafetoprotein. His symptom was caused by a ruptured massive intraabdominal ...
متن کاملPrimary pure gastric yolk sac tumor
We describe here a case of pure gastric yolk sac tumor (YST). A 62-year-old patient underwent gastrectomy with D2 dissection. The histological report confirmed the diagnosis of YST and that two of the 14 regional lymph nodes removed were metastatic. Three courses of PEB regimen chemotherapy were delivered subsequently. Three months later the patient experienced dysphagia from stenosis of the an...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association)
سال: 1999
ISSN: 1882-5133,1345-2843
DOI: 10.3919/jjsa.60.2458