Volume 55, Issue 6 pp. 1191-1194
Brief Report

May–Thurner syndrome found incidentally after left femoral catheterization in a pediatric patient

Kun Moo Lee MD, PhD

Kun Moo Lee MD, PhD

Department of Anesthesiology, Paik Hospital, Inje University, Busan, Korea

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Ji Kyoung Park MD

Ji Kyoung Park MD

Department of Pediatric Blood and Cancer, Paik Hospital, Inje University, Busan, Korea

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Se Hun Lim MD

Se Hun Lim MD

Department of Anesthesiology, Paik Hospital, Inje University, Busan, Korea

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Kwang Rae Cho MD

Kwang Rae Cho MD

Department of Anesthesiology, Paik Hospital, Inje University, Busan, Korea

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Yong Han Kim MD

Yong Han Kim MD

Department of Anesthesiology, Haeundae Paik Hospital, Inje University, Busan, Korea

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Soon Ho Cheong MD, PhD

Corresponding Author

Soon Ho Cheong MD, PhD

Department of Anesthesiology, Paik Hospital, Inje University, Busan, Korea

Department of Anesthesiology, Paik Hospital, Inje University, Gaegumdong, Jingu, Busan 614-735, Korea.===Search for more papers by this author
First published: 25 October 2010
Citations: 3

Conflict of interest: Nothing to report.

Abstract

In May–Thurner syndrome, the left common iliac vein is compressed between the overlying right common iliac artery and the underlying vertebral body. Chronic and/or repetitive compressions at this site cause fibrosis of the vein and thus stenosis, potentially occluding the lumen. This report describes a case of May–Thurner syndrome discovered incidentally after femoral catheterization for chemotherapy in a 25-month-old child with juvenile myelomonocytic leukemia (JMML). The patient had no symptoms associated with compression. The syndrome was diagnosed by computed tomography, and there was no evidence of thrombosis. The patient died secondary to sepsis. Pediatr Blood Cancer. 2010;55:1191–1194. © 2010 Wiley-Liss, Inc.

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