Images in Clinical Practice Indian Pediatrics 2000;37: 1139-1140 |
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Cystic Hygroma |
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A cystic hygroma of the neck is soft, watery and easily transilluminated; there is no other lesion that is quite so characterstic. It consists of thin-walled cysts with flat endothelium. During surgery, it often seems that the mass has the consistency of water-filled soap bubbles and there is no end to the infiltration of normal tissue. In spite of the extensive invasion of tissue planes, these are benign lesions. About 75% of cystic hygromas are in the neck, 20% in the axilla (Fig. 2) and 5% on the trunk or extremity. Some 50 to 60% of cystic hygromas are present at birth, and practically, all of them are apparent by two years of age. Yogesh Kumar Sarin,
A newborn baby presented with multiple congenital anomalies. The child had bilateral cleft lip and palate, broad flat nose, coloboma in right eye, low set ears, polysyndactyly in all four limbs (Fig. 1) and dextrocardia with apparent ambiguous genitalia. Karyotyping revealed trisomy of chromosome 13 and intercallary deletion of chromosome 12. This confirmed the diagnosis of Trisomy 13, also known as Patau syndrome. The incidence at birth is around one in 2000. In addition to the above mentioned features, one may also observe micro-ophthalmia, holopro-sencephaly, hypotelorism, hypoplastic or absent ribs and visceral malformations.
Manjusha Goel,
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