Literature DB >> 21129536

Concordance for neuroblastoma in monozygotic twins: case report and review of the literature.

Tatsuro Tajiri1, Ryota Souzaki, Yoshiaki Kinoshita, Sakura Tanaka, Yuhki Koga, Aiko Suminoe, Toshiro Hara, Kenichi Kohashi, Yoshinao Oda, Kouji Masumoto, Miki Ohira, Akira Nakagawara, Tomoaki Taguchi.   

Abstract

The patients were infant male twins born by cesarean delivery following a healthy pregnancy at 36 weeks' gestation to unrelated parents. At 4 months of age, twin 2 presented with hepatomegaly and a right suprarenal mass. Resection of an adrenal tumor and a liver tumor biopsy were performed. Twin 1 had no symptoms at 4 months of age. Screening by abdominal ultrasonography showed multiple masses in the liver but no adrenal mass. Metaiodobenzylguanidine scintigraphy showed positive findings in multiple liver masses. A laparoscopic biopsy for a liver tumor was performed. All primary tumor and liver tumor specimens from twin 2 and the liver tumor of twin 1 had the same histologic classification of neuroblastoma and nearly identical genetic aberrations, including a chromosome gain or loss using array-comparative genomic hybridization. From these clinical and pathologic findings and genetic analyses, we strongly demonstrate the transplacental metastatic spread from twin 2 to twin 1. In the literature, 9 pairs of concordant twin neuroblastomas, including the current twin, have been presented; and the clinical findings of 5 twin pairs may represent placental metastases from one twin with congenital neuroblastoma to the other twin. This study is the first report presenting the possibility of twin-to-twin metastasis in monozygotic twins with neuroblastoma based on an analysis of the clinical features and genetic aberrations.
Copyright © 2010 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 21129536     DOI: 10.1016/j.jpedsurg.2010.08.025

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  5 in total

Review 1.  Imaging of Horner syndrome in pediatrics: association with neuroblastoma.

Authors:  Hedieh Khalatbari; Gisele E Ishak
Journal:  Pediatr Radiol       Date:  2020-10-06

2.  Genomic analysis-integrated whole-exome sequencing of neuroblastomas identifies genetic mutations in axon guidance pathway.

Authors:  Yuanyuan Li; Miki Ohira; Yong Zhou; Teng Xiong; Wen Luo; Chao Yang; Xiangchun Li; Zhibo Gao; Rui Zhou; Yohko Nakamura; Takehiko Kamijo; Yasuhiko Kaneko; Takeshi Taketani; Junichi Ueyama; Tatsuro Tajiri; Hongyan Zhang; Jian Wang; Huanming Yang; Ye Yin; Akira Nakagawara
Journal:  Oncotarget       Date:  2017-05-23

3.  Family history of cancer and the risk of childhood solid tumours: a Norwegian nationwide register-based cohort study.

Authors:  Ruby Del Risco Kollerud; Karl Gerhard Blaasaas; Bjørgulf Claussen; Per Nafstad; Lisa A Cannon-Albright; Ellen Ruud; Finn Wesenberg; Øyvind Næss
Journal:  Br J Cancer       Date:  2018-02-20       Impact factor: 7.640

4.  Monozygotic twins with neuroblastoma MS have a similar molecular profile: a case of twin-to-twin metastasis.

Authors:  Margaret Shatara; Ana C Xavier; Alan Dombkowski; Daniela Cukovic; Janet M Poulik; Deniz Altinok; Yubin Ge; Jeffrey W Taub
Journal:  Br J Cancer       Date:  2019-10-11       Impact factor: 7.640

Review 5.  Clinical, Histological, Cytogenetic and Molecular Analysis of Monozygous Twins with Wilms Tumor.

Authors:  Katarzyna Iwańczyk; Bartosz Czachowski; Patrycja Sosnowska-Sienkiewicz; Gabriela Telman; Paulina Ciążyńska; Przemysław Mańkowski; Danuta Januszkiewicz-Lewandowska
Journal:  Genes (Basel)       Date:  2022-02-18       Impact factor: 4.096

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.