نتایج جستجو برای: cystic hygroma
تعداد نتایج: 47346 فیلتر نتایج به سال:
Isolated fetal lateral neck cysts can represent a cystic hygroma or a developmental remnant cyst. In the absence of an increased nuchal translucency or associated malformations the risk of aneuploidy has been considered negligible. Still, dysmorphology in aneuploid fetuses might not be evident except at a later stage. We report on a case of isolated fetal bilateral neck cysts where aneuploidy w...
A 3-day-old child presented with a gross swelling on the right side of the neck extending beyond the midline and inability to swallow. It was diagnosed to be cystic hygroma and decision was made to excise the swelling as an emergency operation to enable the child to swallow and thrive better. During the gaseous induction, difficulty was encountered in maintaining the airway and subsequently to ...
Aim and Background: Cystic hygroma is a congenital malformation of the lymphatic system in which obstruction between the lymphatic and venous pathway in fetal neck leads to lymph accumulation in the jugular sac of nuchal region. Case report: A 8- years- old infant with a huge anterior cervical mass is presented. He became candidate for tumor excision under general anesthesia as the mass did not...
Posterior midline cervical cystic hygromas (PMC) are frequently found associated with chromosomal aberrations and usually do not survive. The present report illustrates diagnosis of this condition by sonography in an 18 weeks old fetus and an amniocentesis revealed 45 x0 karyotype and increased concentration of alpha-fetoproteins. Pregnancy was terminated in view of Turner's syndrome. The etiol...
Cavernous lymphangioma (cystic hygroma) is a rare form of mesenteric cystic tumor, which can be located anywhere along the intestinal mesenterium or elsewhere in the body. Mesenteric cystic tumors are rare malformations. They are more common in pediatric population with estimated incidence to be 1 in 20.000 patients, rarely they occur in adults with estimated incidence to be 1 in 100.000 patien...
Objective Noonan syndrome (NS) is a common, autosomal dominant, frequently de novo condition due to mutations in RAS-MAPK pathway genes. Presentation is variable, usually in infancy or early childhood, and includes poor postnatal growth, cardiac abnormalities, dysmorphic features and lymphatic dysplasia. The classic cardiac abnormalities are pulmonary valve dysplasia and hypertrophic cardiomyop...
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