Cribriform-morular Thyroid Carcinoma Arising in a Medulloblastoma Survivor: Two Metachronous Tumors Shared with the Activation of the Wnt Signaling Pathway

Author:

Luo Minghua1,Chen Yaoli1,Yin Xiaomin1,Li Jian12ORCID

Affiliation:

1. Department of Pathology, Peking University Shenzhen Hospital, Shenzhen, Guangdong Province, China

2. State Key Laboratory of Chemical Oncogenomics, Peking University Shenzhen Graduate School, Shenzhen, Guangdong Province, China

Abstract

Wnt signaling pathway activation is involved in the pathogenesis of a series of malignant tumors and is characterized by the nuclear accumulation of β-catenin protein. The occurrence of two or more Wnt pathway-associated tumors in a single individual is uncommon and generally attributed to inherited cancer syndrome, especially familial adenomatous polyposis (FAP). Herein, we presented a rare case of a child who suffered from the occurrence of Wnt-activated medulloblastoma and cribriform-morular thyroid carcinoma (CMTC) within a 9-year interval. She had no history of FAP and harbored an unexpected somatic mutation of the APC gene in the CMTC tumor. The potential agents involved in the pathogenesis of the two molecular-linked tumors other than FAP were discussed in this report.

Funder

Open Research Fund of State Key Laboratory of Chemical Oncogenomics

Shenzhen Science and Technology Program

the Key Program for Clinical Research at Peking University Shenzhen Hospital

Publisher

SAGE Publications

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