Congenital prenatal hemangioma: Diagnosis and treatment

被引：2
|
作者：
Bourdelat, D. [1 ]
Melki, E. [2 ]
Mazzola, C. [1 ]
Marreel, A. [3 ]
机构：
[1] Ctr Hosp & Univ Pointe a Pitre, Serv Chirurg Pediat, F-97110 Pointe A Pitre, Guadeloupe, France
[2] Ctr Hosp & Univ, Serv Gynecol Obstet, F-97110 Pointe A Pitre, Guadeloupe, France
[3] Ctr Hosp & Univ, Serv Anat & Cytol Pathol, F-97110 Pointe A Pitre, Guadeloupe, France
来源：
ARCHIVES DE PEDIATRIE | 2010年 / 17卷 / 04期
关键词：
KASABACH-MERRITT-SYNDROME;
D O I：
10.1016/j.arcped.2010.01.004
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
An echogenic tumor (22 x 22 mm) isolated from the anterior part of the left leg at 27 WA of pregnancy suggested an angiomatous structure. This mass appeared to be well vascularized on Doppler examination. Three-dimensional imaging showed connections with adjacent tissues. The limbs were mobile. Delivery of a 3990-g-boy occurred normally. On the anterior part of the left leg, there was a plate-shaped mass with a pink hole at the superior part. Excision under general anesthesia was performed at the first month because of the risk of rupture and bleeding. The dissection was easy with the deep plane. Healing was complete 10 days after the surgical procedure and the aesthetic aspect was good 1 year later. Histological findings of the suspect mass emphasize the vascular aspect of the tumor. A hemangioma capillary with venous structures in the dermal hypodermic area was found. (C) 2010 Published by Elsevier Masson SAS.
引用
收藏
页码：383 / 386
页数：4
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