Pulmonary blastoma with yolk sac elements
نویسندگان
چکیده
منابع مشابه
YOLK 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 کاملPulmonary pure yolk-sac tumor. A rare anatomopathological entity.
The most frequent location for non-metastatic germ cell tumors is the anterior mediastinum. Primary lung germ cell tumors are an exception in medical literature being limited to just a few cases of choriocarcinomas and rare cases of yolk-sac tumors. In this paper, we report a case of a pulmonary yolk-sac tumor with atypical characteristic as regards its diagnosis and treatment.
متن کاملGastric Adenocarcinoma with Yolk Sac Tumor Differentiation and Liver Metastasis of Yolk Sac Tumor Component
Gastric adenocarcinoma with yolk sac tumor (YST) differentiation has rarely been reported. We report a case of primary gastric adenocarcinoma with yolk sac tumor differentiation and liver metastases of the YST component in a 50-years-old patient. This was suspected due to high serum level of alpha fetoprotein in the presence of a gastric fundal tumor. Gastric carcinoma with yolk sac tumor compo...
متن کاملClassic pulmonary blastoma: a subtype of biphasic pulmonary blastoma.
We report a rare case of classic pulmonary blastema (CPB) without recurrence for 3 years after the operation. A 70-year-old man presented with cough and sputum for a month. Chest computed tomography (CT) showed a 5cm-sized mass in the right middle lobe. Bronchoscopic examination was performed, and the mass was suspected as adenocarcinoma of the lung. Right middle lobectomy and lymph node dissec...
متن کاملEndometrial Yolk Sac Tumor with Omental Metastasis
To the Editor: A 38‐year‐old woman presented at our hospital with a complaint of hypermenorrhea lasting 2 months. No symptoms were found by bimanual examination, and vaginal ultrasound showed endometrial thickness of 4 mm. Diagnostic curettage strongly suggested clear‐cell adenocarcinoma. Magnetic resonance imaging of the pelvis showed an intact endometrial binding zone with no extrauterine inf...
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ژورنال
عنوان ژورنال: Indian Journal of Pathology and Microbiology
سال: 2010
ISSN: 0377-4929
DOI: 10.4103/0377-4929.72027