Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA

Author:

Nriagu Bede N.12,Williams Lydia S.2,Brewer Niambi3,Surrey Lea F.24,Srinivasan Abhay S.25,Li Dong1,Britt Allison26,Treat James27,Crowley T. Blaine6,O'Connor Nora1,Ganguly Arupa3,Low David28,Queenan Maria24,Drivas Theodore G.6,Zackai Elaine H.6,Adams Denise M.29,Hakonarson Hakon126,Snyder Kristen M.29,Sheppard Sarah E.10ORCID

Affiliation:

1. Center for Applied Genomics, Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

2. Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

3. Genetic Diagnostic Laboratory University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA

4. Department of Pathology and Laboratory Medicine Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

5. Department of Radiology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

6. Division of Human Genetics Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

7. Section of Dermatology, Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

8. Division of Plastic and Reconstructive Surgery Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

9. Division of Oncology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

10. Unit on Vascular Malformations, Division of Intramural Research Eunice Kennedy Shriver National Institute of Child Health and Human Development Bethesda Maryland USA

Abstract

AbstractTurner syndrome (45,X) is caused by a complete or partial absence of a single X chromosome. Vascular malformations occur due to abnormal development of blood and/or lymphatic vessels. They arise from either somatic or germline pathogenic variants in the genes regulating growth and apoptosis of vascular channels. Aortic abnormalities are a common, known vascular anomaly of Turner syndrome. However, previous studies have described other vascular malformations as a rare feature of Turner syndrome and suggested that vascular abnormalities in individuals with Turner syndrome may be more generalized. In this study, we describe two individuals with co‐occurrence of Turner syndrome and vascular malformations with a lymphatic component. In these individuals, genetic testing of the lesional tissue revealed a somatic pathogenic variant in PIK3CA—a known and common cause of lymphatic malformations. Based on this finding, we conclude that the vascular malformations presented here and likely those previously in the literature are not a rare part of the clinical spectrum of Turner syndrome, but rather a separate clinical entity that may or may not co‐occur in individuals with Turner syndrome.

Funder

Children's Hospital of Philadelphia

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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