Concomitant aortocaval resection for germ cell tumour

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Predisposition alleles for Testicular Germ Cell Tumour.

For some time, it has been known that there is a substantial genetic component to testicular germ cell tumour susceptibility, supported by several pieces of evidence, including the significantly increased familial risk and differential risk among races. However, despite extensive linkage searches on available families, no high penetrance genes have been identified. Recently genome-wide associat...

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Up to 3.2% of patients with testicular germ cell tumours represent with late-relapsing disease. Aggressive surgical resection confers the greatest chance of cure in this patient group. We present the case of a late and extensively relapsed nonseminomatous germ cell tumour with thrombus present along the entire length of the inferior vena cava, as well as in the right hepatic vein. Techniques pr...

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Mediastinal germ cell tumour and myelodysplastic syndrome.

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A Big Catch for Germ Cell Tumour Research

1 Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America, 2 Center for Cancer and Blood Disorders, Children’s Medical Center, Dallas, Texas, United States of America, 3 Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America, 4 Department of Internal Medicine, University...

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A rare case of adult onset Langerhans' cell histiocytosis associated with dysgerminoma in a 35 year old Chinese woman is reported. The patient had a history of dysgerminoma of left ovary 15 years previously and had undergone surgery followed by radiotherapy and an uneventful recovery. She presented again in March 1994, this time with a left clavicular mass, which was shown histologically to be ...

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ژورنال

عنوان ژورنال: Indian Journal of Medical Research

سال: 2020

ISSN: 0971-5916

DOI: 10.4103/ijmr.ijmr_1953_19