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J Pediatr Hematol Oncol ; 39(2): e82-e84, 2017 03.
Article in English | MEDLINE | ID: mdl-27322711

ABSTRACT

Tumors arising from urachus in children are exceedingly rare and sporadically reported in literature. Being a midline structure, the urachus may harbor neoplastic germ cell elements and can occasionally present as a case of acute abdomen. A 20-month-old toddler presented with spontaneous rupture of an urachal yolk sac tumor causing hemoperitoneum. He underwent resection, received platinum-based chemotherapy and presently remains well on follow-up. Despite its rarity, urachal germ cell tumors must be considered in a child with acute abdomen and tumor markers must be measured preemptively in such cases.


Subject(s)
Endodermal Sinus Tumor/complications , Hemoperitoneum/etiology , Urachus/diagnostic imaging , Urinary Bladder Neoplasms/complications , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Biomarkers, Tumor/analysis , Bleomycin/administration & dosage , Carboplatin/administration & dosage , Combined Modality Therapy , Consanguinity , Emergencies , Endodermal Sinus Tumor/chemistry , Endodermal Sinus Tumor/diagnostic imaging , Endodermal Sinus Tumor/therapy , Etoposide/administration & dosage , Humans , Infant , Laparotomy , Male , Rupture, Spontaneous , Tomography, X-Ray Computed , Urinary Bladder Neoplasms/chemistry , Urinary Bladder Neoplasms/diagnostic imaging , Urinary Bladder Neoplasms/therapy
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