Congenital infantile fibrosarcoma in a very low-birth-weight infant

被引：7

作者：

Mukai, Motoi ^{[1
,2
]}

Sameshima, Hiroshi ^{[2
]}

Kodama, Yuki ^{[2
]}

Yamashita, Rie ^{[2
]}

Kaneko, Masatoki ^{[2
]}

Ikenoue, Tsuyomu ^{[2
]}

Matsufuji, Hiroshi ^{[1
]}

Kondo, Kazuhiro ^{[3
]}

Chijiiwa, Kazuo ^{[3
]}

机构：

[1] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Pediat Surg, Kagoshima 8908520, Japan

[2] Miyazaki Univ, Sch Med, Univ Miyazaki Hosp, Perinatal Ctr, Miyazaki, Japan

[3] Miyazaki Univ, Sch Med, Dept Surg Oncol & Regulat Organ Funct, Miyazaki, Japan

来源：

JOURNAL OF PEDIATRIC SURGERY | 2012年 / 47卷 / 04期

关键词：

Congenital; Fibrosarcoma; Infantile; Fetal; Intrauterine; PRENATAL SONOGRAPHIC APPEARANCE; HYDROPS-FETALIS; DIAGNOSIS; HEMANGIOMA; ULTRASOUND;

D O I：

10.1016/j.jpedsurg.2011.11.052

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

We describe a prenatally diagnosed case with congenital infantile fibrosarcoma, which is a rare malignant tumor, of which there have been only 14 cases reported in the English literature. A giant mass on the left thigh was detected at 24 weeks' gestation by prenatal ultrasonography. Because of its rapid growth and nonreassuring fetal status in utero, the baby was delivered by cesarean delivery at 27 weeks' gestation. The case was complicated by hemorrhagic anemia, coagulopathy, and cardiac failure, and a tumor resection was performed on day 3. As of age 2.5 years, he was healthy without evidence of recurrence. Because some fetal cases with congenital infantile fibrosarcoma have a poor prognosis, termination of pregnancy at an appropriate time and postnatal early treatment are crucial for successful treatment. (C) 2012 Elsevier Inc. All rights reserved.

引用

页码：E1 / E4

页数：4

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