• World Neurosurg · Nov 2017

    Case Reports

    An unusual combination of mirror-image dextrocardia with familial medulloblastoma : Is there a histogenetic relationship?

    • Chao Ke, Jing Wang, Shaoyan Xi, Kay Ka-Wai Li, Junran Luo, Zhenghe Chen, Jian Wang, and Zhong-Ping Chen.
    • Department of Neurosurgery, Sun Yat-Sen University Cancer Center, Guangzhou, China; State Key Laboratory of Oncology in South China and Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.
    • World Neurosurg. 2017 Nov 1; 107: 860-867.

    BackgroundThe occurrence of medulloblastoma in the absence of hereditary syndromes is rare. Dextrocardia with situs inversus is also called mirror-image dextrocardia. A combination of mirror-image dextrocardia with medulloblastoma has not been reported previously. To the best of our knowledge, this is the first report of this rare combination in a family with medulloblastoma.MethodsThe clinical manifestation, radiographic characteristics, treatment, and outcomes of 3 medulloblastoma cases in 2 cousins and their maternal uncle was described. Tumor samples of the 2 cousins were first examined for histologic subtypes. Total RNA of their tumors was extracted from formalin-fixed and paraffin-embedded samples. Then, expression of 22 subgroup-specific genes and 3 housekeeping genes was analyzed by the NanoString nCounter Analysis System. The posttest data were normalized by NanoStringNorm package for molecular subgroup prediction.ResultsThe proband remains tumor free and alive up to the latest follow-up. His cousin, who had combined mirror-image dextrocardia with situs inversus, died of anoxia after surgery and his uncle died of tumor 2.5 years after surgery. Medulloblastoma of the 2 cousins was classified as classic and molecular group 4 subtype.ConclusionsThe same classic and molecular group 4 subtype of the 2 cousins may suggest a similar genetic predisposition. Involvement of the Otx2 gene dysfunction in both group 4 subtype medulloblastoma and mirror-image dextrocardia with situs inversus points to a possible mechanism that dysfunction of a shared signaling pathway such as Otx2 might be the underlying cause of these 2 conditions in this family.Copyright © 2017 Elsevier Inc. All rights reserved.

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