Paratesticular congenital malignant rhabdoid tumor diagnosed by fine-needle aspiration cytology. A case report

✍ Scribed by Javier Salamanca; José Luis Rodríguez-Peralto; Daniel Azorín; Claudio Ballestín; Pedro De Agustín

• Publisher: John Wiley and Sons
• Year: 2003
• Tongue: English
• Weight: 272 KB
• Volume: 30
• Category: Article
• ISSN: 8755-1039
• DOI: 10.1002/dc.10410

✦ Synopsis

Abstract

We report the FNA features of a congenital malignant extrarenal rhabdoid tumor (MERT) located in the right paratesticular area of a newborn full‐term boy (39 wk gestation), with disseminated metastases in the liver and right parietal region. The diagnosis was suggested two days after birth by fine‐needle aspiration biopsy (FNAB) of the parietal mass, which demonstrated an atypical large cell proliferation with vesicular nuclei, prominent nucleoli, and abundant cytoplasm exhibiting paranuclear dense inclusions. The diagnosis was confirmed by histopathologic and immunohistochemical examination of the primary paratesticular tumor. To the best of our knowledge, this is the third MERT reported in the paratesticular region, one of the few congenital extrarenal non‐central nervous system cases, and the third congenital case (renal or extrarenal) primarily diagnosed by FNAB. We emphasize the characteristic cytologic features of a congenital rhabdoid tumor, which must be known by pathologists because of the clinical and prognostic implications. Diagn. Cytopathol. 2004;30:46–50. © 2004 Wiley‐Liss, Inc.