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3 results on '"Kaltari DK"'

1. Laparoscopic excision of intra-abdominal oesophageal duplication cyst in a child.

Author

Pujar VC, Kurbet S, and Kaltari DK

Abstract

Duplication cysts are congenital cystic malformation of the alimentary tract consisting of a duplication of the segment to which it is adjacent. It can occur anywhere from mouth to anus. Oesophageal duplication cysts comprise 4% of the same. Of these, total intra-abdominal oesophageal duplication cysts are extremely rare. On review of literature, only 3 case reports of total intra-abdominal oesophageal duplication managed laparoscopically are found. All these cases were adults. We report the first paediatric case of intra-abdominal oesophageal duplication cyst excised laparoscopically.

Published
2013
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2. Cloacal dysgenesis sequence in a set of twins: new insights into embryology and a review of the literature.

Author

Gupta R, Parelkar SV, Oak S, Sanghvi B, Kaltari DK, Prakash A, Patil R, and Bachani M

Subjects
Digestive System Abnormalities, Diseases in Twins genetics, Fatal Outcome, Gastroschisis embryology, Humans, Infant, Newborn, Limb Deformities, Congenital, Male, Urogenital Abnormalities, Abnormalities, Multiple genetics, Cloaca abnormalities, Diseases in Twins embryology
Published
2010
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3. Ruptured rectal duplication cyst with classical bladder exstrophy.

Author

Gupta RK, Oak S, Parelkar SV, Sanghvi B, Kaltari DK, Prakash A, Patil R, and Bachani M

Subjects
Cloaca embryology, Humans, Infant, Newborn, Male, Perineum embryology, Perineum surgery, Rectum embryology, Rectum surgery, Rupture, Spontaneous, Urologic Surgical Procedures, Male methods, Abnormalities, Multiple embryology, Abnormalities, Multiple surgery, Bladder Exstrophy embryology, Bladder Exstrophy surgery, Perineum abnormalities, Rectum abnormalities
Abstract

A newborn boy was brought to us, 2 hours after birth, with a mucosal-lined left hemiperineal lesion associated with classical bladder exstrophy and an anterolaterally displaced anus. Perineal anatomy was restored by excising the mucosa lined lesion. The bladder closure for classical bladder exstrophy was done at the same time. Histologically, gastric, respiratory, and small intestinal epithelia were present in the mucosa. A rectal duplication cyst that had ruptured in utero through the hemiperineum could explain the anomaly. The association of classical bladder exstrophy with ruptured rectal duplication cyst has never previously been described in the literature., (Copyright 2010 Elsevier Inc. All rights reserved.)

Published
2010
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