J Korean Med Sci.  2002 Jun;17(3):400-402. 10.3346/jkms.2002.17.3.400.

Fetal Axillary Cystic Hygroma Detected by Prenatal Ultrasonography: A Case Report

Affiliations
  • 1Department of Obstetrics and Gynecology, Chonnam National University Medical School and Research Institute of Medical Sciences, Chonnam National University, Korea. tbsong@chonnam.chonnam.ac.kr
  • 2Department of Diagnostic Radiology, Chosun University Medical School, Gwangju, Korea.

Abstract

Fetal cystic hygroma is a rare developmental congenital anomaly of the lymphatic system, characterized by the formation of a multilocular, variable sized cystic mass. Most of cystic hygromas are found in the neck and other rare locations include axilla, mediastinum, and limbs. There are many papers about cystic hygroma colli, but there are only a few papers about fetal axillary cystic hygroma and no domestic papers. We present a case of fetal axillary cystic hygroma diagnosed antenatally followed by full-term delivery in a 30-yr-old woman. Operation was performed on the 8th day after birth and the mass was excised and confirmed as cystic hygroma.

Keyword

Lymphangioma; Cystic; Axillary; Fetal Lymphangioma; Cystic; Prenatal Diagnosis

MeSH Terms

Adult
Axilla
Female
Humans
Infant, Newborn
Lymphangioma, Cystic/*pathology/*ultrasonography
Pregnancy
Pregnancy Complications
*Ultrasonography, Prenatal
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