Volume 60, Issue 1 pp. 146-148
Brief Report

Clinical, histologic, and genetic features of mesothelioma in a 7-Year-old child

Aaron Sugalski DO

Aaron Sugalski DO

Department of Pediatrics and Greehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, Texas

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Mary Davis MD

Mary Davis MD

Helen DeVos Children's Hospital at Spectrum Health, Grand Rapids, Michigan

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Latha Prasannan MD

Latha Prasannan MD

Covenant Children's Hospital, Lubbock, Texas

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Victor Saldivar MD

Victor Saldivar MD

CHRISTUS Santa Rosa Children's Hospital, San Antonio, Texas

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Jaclyn Y. Hung PhD

Jaclyn Y. Hung PhD

Department of Pediatrics and Greehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, Texas

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Gail E. Tomlinson MD, PhD

Corresponding Author

Gail E. Tomlinson MD, PhD

Department of Pediatrics and Greehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, Texas

Department of Pediatrics and Greehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, 8403 Floyd Curl Drive, San Antonio, TX 78229.===Search for more papers by this author
First published: 07 September 2012
Citations: 8

Abstract

Malignant mesothelioma (MM) is a highly aggressive malignancy that is extremely rare in children. This case report documents a 7-year-old male without previous asbestos exposure with peritoneal MM that initially responded to chemotherapy with cisplatin and gemcitabine but ultimately metastasized to his chest. He was diagnosed with MM based on histology, extensive immunohistochemical analyses, and an elevated serum CA-125 level. Cytogenetics and comparative genomic hybridization (CGH) analysis of his tumor identified a single extra copy number of chromosome 11 with few other changes noted. Pediatr Blood Cancer 2013; 60: 146–148. © 2012 Wiley Periodicals, Inc.

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