Prenatal ultrasonographic diagnosis of axillary cystic hygroma

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Prenatal ultrasonographic diagnosis of axillary cystic hygroma

Cystic hygromas are anomalies of the lymphatic system characterized by single or multiple cysts within soft tissue. The prenatal diagnosis of cystic hygroma by ultrasound is well documented in literature. Approximately 75-80% of all cystic hygromas involve the neck and the lower portion of the face, 15-20 % occur in the axilla , while remaining 5% are found in the mediastinum, retropertoneum,ab...

متن کامل

Prenatal diagnosis of alobar holoprosencephaly with cystic hygroma.

OBJECTIVE Holoprosencephaly is a kind of brain anomaly characterized by inadequate cleavage of the prosencephalon during early embryogenesis. In addition, holoprosencephaly associated with cystic hygroma and hydrops fetalis has never been reported. In this article, we report a rare case of holoprosencephaly associated with cystic hygroma and hydrops fetalis diagnosed prenatally. CASE REPORT A...

متن کامل

Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report.

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 a...

متن کامل

Fetal axillary cystic hygroma: a case report and review

Cystic hygroma (CH) is a lymphatic malformation occurring different parts of fetal body, typically in the region of the fetal neck and axillary, abdominal wall, mediastinal, inguinal and retroperitoneal areas. CH has been associated with fetal aneuploidy, hydrops fetalis, structural malformations and intrauterine fetal death.A 24-year-old gravida 1, para 1 was admitted to our hospital at 28 wee...

متن کامل

Prenatal diagnosis of 18p deletion and isochromosome 18q mosaicism in a fetus with a cystic hygroma.

Although, deletion of short arm of chromosome 18 is one of the most frequent autosomal terminal deletions, mosaic form of 18p deletion is infrequently observed. Furthermore, prenatally detected cases of 18p deletion and isochromosome 18q mosaicism are extremely rare. Herein, we present a case of del(18p)/i(18q) mosaicism, prenatally detected after chori- onic villus sampling. A 37-year-old woma...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Nepal Journal of Obstetrics and Gynaecology

سال: 1970

ISSN: 1999-8546,1999-9623

DOI: 10.3126/njog.v2i1.1478