Malignant rhabdoid tumor of the liver: a case report and literature review

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Satoru Oita
Keita Terui *
Syugo Komatsu
Tomoro Hishiki
Takeshi Saito
Tetsuya Mitsunaga
Mitsuyuki Nakata
Hideo Yoshida
(*) Corresponding Author:
Keita Terui | kta@cc.rim.or.jp

Abstract

Malignant rhabdoid tumor (MRT) is a rare and aggressive malignancy associated with poor outcomes. MRT of the liver is even rarer, and little information has been described. We report the case of an 8-month-old boy with MRT of the liver. The tumor showed aggressive progression despite a multidisciplinary approach, and the patient died due to multiple organ failure 14 days after admission. Autopsy revealed the liver tumor and multiple metastases with negative immunohistochemistry for INI1/BAF47. A review of 53 cases of pediatric MRT of the liver is provided.

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