The Japanese Journal of Pediatric Hematology / Oncology
Online ISSN : 2189-5384
Print ISSN : 2187-011X
ISSN-L : 2187-011X
Case Report
Watchful observation for hepatoblastoma with trisomy 18: A report of two cases
Kosuke TamefusaYusei NakataKiyoshi SasakiChiho TokorodaniRitsuo Nishiuchi
Author information
JOURNAL FREE ACCESS

2021 Volume 58 Issue 1 Pages 55-59

Details
Abstract

Trisomy 18 (T18) is a chromosomal disorder with poor prognosis, and more than 90% of T18 patients have congenital heart disease (CHD). Some patients develop malignant tumors such as hepatoblastoma (HB) and Wilms tumor. Recently, the application of radical or palliative surgery for CHD has improved patient prognosis, and an increasing number of patients have received home healthcare. Here, we describe the cases of two T18 patients diagnosed in the fetal period who developed HB during the clinical course. Both patients progressed to home healthcare without selecting surgical treatment for CHD. In addition, nontreatment supportive care was selected for HB. The natural clinical course of HB with T18 is unclear, but both patients survived for more than 2 years after diagnosis. There are few reports on the natural clinical course of HB associated with T18, and thus we believe that this report may provide information that can be used as a reference for future treatment policy selection.

Content from these authors
© 2021 The Japanese Society of Pediatric Hematology / Oncology
Previous article Next article
feedback
Top