Massive unilateral fetal axillary lymphangioma: A case report

被引：0

作者：

Hutchison, Dana M. ^{[1
,5
]}

Crosland, Brian A. ^{[2
,3
]}

Wang, Larry ^{[4
]}

Nageotte, Michael P. ^{[3
]}

机构：

[1] Univ Calif Irvine, Sch Med, Tustin, CA USA

[2] Univ Calif Irvine, Dept Obstet & Gynecol, Div Maternal Fetal Med, Irvine, CA USA

[3] Miller Childrens & Womens Hosp, Long Beach Mem Med Ctr, Long Beach, CA USA

[4] Childrens Hosp Los Angeles, Dept Pathol, Los Angeles, CA USA

[5] 1001 Hlth Sci Rd, Irvine, CA 92617 USA

来源：

CASE REPORTS IN WOMENS HEALTH | 2021年 / 31卷

关键词：

Fetal axillary cystic hygroma; Axillary lymphangioma; Prenatal diagnostics; Ultrasound; Case report;

D O I：

暂无

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

We report a substantial axillary lymphangioma in a fetus delivered at 38 weeks of gestation. Detailed fetal survey at 20 weeks revealed a 5.45 x 3.72 cm nonvascular cystic axillary structure without other malformations; amniocentesis was negative. Serial surveillance was performed throughout the pregnancy. A male infant weighing 3000 g with a 16 x 12 x 9 cm septated cystic mass arising from the left axilla was delivered via cesarean section. The newborn period was complicated by cellulitis overlying the mass and interval cystic hemorrhage requiring sclerotherapy and subsequent excision. Nonnuchal lymphangiomas may be etiologically distinct entities. The prognostic factors include anatomic location, presence of septa, and association with other congenital abnormalities. A thorough evaluation, multidisciplinary approach, and close surveillance should be undertaken to optimize neonatal outcomes.(c) 2021 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).

引用

页数：4