Literature DB >> 29701292

Therapeutic experience with hepatoblastoma associated with trisomy 18.

Akiko Inoue1, Ryo Suzuki1, Keisuke Urabe1, Yutaro Kawamura1, Midori Masuda1, Kanta Kishi1, Kimitaka Takitani1, Hiroshi Katayama1, Hideki Tomiyama2, Michihiro Hayashi2, Shintaro Nemoto3, Kazuhisa Uchiyama2, Hiroshi Tamai1.   

Abstract

Trisomy 18 is often fatal, but patients with this disease can now have longer survival due to proactive treatment intervention. However, hepatoblastomas may develop in these patients. In this study, we report four cases of hepatoblastoma associated with trisomy 18. All of the patients had congenital heart disease and three had undergone intracardiac surgical repair. Tumor growth was relatively slow in all cases, and there were no problems with chemotherapy tolerability and surgical resection. Three of the patients are currently disease-free and the fourth is alive with remaining of the tumor. These cases suggest that combined chemotherapy and surgical resection may be an option to treat hepatoblastoma associated with trisomy 18 when cardiac pulmonary function is relatively stable.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  congenital heart disease; hepatoblastoma; trisomy 18

Mesh:

Year:  2018        PMID: 29701292     DOI: 10.1002/pbc.27093

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  2 in total

1.  Case Report of Congenital Hepatoblastoma With the Onset at 30-Weeks' Gestation.

Authors:  Zheng Yan; Wei Bai; Li Li; Shuo Li; Ying Hua; Xiao-Xiao Zhang; Xin-Lin Hou
Journal:  Front Pediatr       Date:  2022-07-01       Impact factor: 3.569

Review 2.  Hepatoblastoma in molecularly defined, congenital diseases.

Authors:  Gunther Nussbaumer; Martin Benesch
Journal:  Am J Med Genet A       Date:  2022-04-28       Impact factor: 2.578

  2 in total

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