Primary Yolk Sac Tumor of the Urachus

Author:

Romero-Rojas Alfredo Ernesto1,Messa-Botero Oscar Alberto1,Melo-Uribe Mario Alexander12,Díaz-Pérez Julio Alexander12,Chinchilla-Olaya Sandra Isabel1

Affiliation:

1. Grupo de Patología del Instituto Nacional de Cancerología INC, Bogotá, Colombia

2. Grupo Patología Estructural Funcional y Clínica de la Universidad Industrial de Santander PATUIS, Bucaramanga, Colombia

Abstract

Introduction. Neoplasms originating from the urachus are rare. The most common urachal malignancy is adenocarcinoma, whereas extragonadal germ cell tumors, primarily of the urachus, are an extremely rare finding. Objective. To describe a primary yolk sac tumor (YST) of the urachus in an adult. Case report. A 44-year-old woman presented with 6 months of pelvic pain associated with a sensation of progressive mass growth. At the time of tumor resection, the tumor was found to be attached by a pedicle to the dome of the bladder, with no injury to the adjacent organs. Pathological study showed a neoplasm with epithelioid cells, pseudocysts, a myxomatous background, and Schiller-Duval body formations. Immunohistochemistry stains showed positivity to AE1/AE3, α-1-fetoprotein, and α-1-antitrypsin and negativity to other markers. Conclusion. An unusual case of a YST in the urachus is presented. This is the first reported adult case based on the authors’ bibliographic search.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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