Sacrococcygeal Teratoma in a Singleton Male Instance of Cornelia de Lange Syndrome: A Case Report

  • Seyed Reza Samsamshariat
Keywords: Sacrococcygeal Teratoma, Cornelia De Lange Syndrome, VATER Association

Abstract

Sacrococcygeal teratoma, sirenomelia, VATER association, anencephaly and holoprocencephaly are occasionally observed in patients with Cornelia de Lange syndrome (CdLS; OMIM 122470). Here, I present an exceptional case of a non-twin, singleton newborn with CdLs who also had a sacrococcygeal teratoma.

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Author Biography

Seyed Reza Samsamshariat

MD, Pathologist
Dr. Samsamshariat Clinical and Surgical Pathology Laboratory
Khorasgan, Esfahan, Iran

CITATION
DOI: 10.26440/IHRJ/0301.04.521069
Published: 2019-04-17
How to Cite
1.
Seyed Reza Samsamshariat. Sacrococcygeal Teratoma in a Singleton Male Instance of Cornelia de Lange Syndrome: A Case Report. IHRJ [Internet]. 2019Apr.17 [cited 2023Feb.1];3(1):20-2. Available from: https://ihrjournal.com/ihrj/article/view/218