Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Vivek Manchanda"'
Publikováno v:
Journal of Neonatal Surgery, Vol 13 (2024)
Background: Anorectal malformations (ARM) are correctable congenital malformations with good prognosis. Traditionally it is managed by staged procedure, with diversion colostomy, followed by definitive procedure and stoma reversal in the third stage.
Externí odkaz:
https://doaj.org/article/33f339eba6c1447abcf1dbe0fb0ee99d
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 28, Iss 5, Pp 357-368 (2023)
Anorectal malformations (ARMs) are managed classically in three stages – colostomy at birth, anorectal pull-through after 2–3 months, and stoma closure. Single-stage pull-through has been contemplated in neonatal age aimed to reduce the number of
Externí odkaz:
https://doaj.org/article/5a33266a61b743a29be24bf65fdd69ae
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 16, Iss 8, Pp 299-301 (2023)
Background: Neonatal appendicitis is a rare diagnosis. There is increased morbidity with associated complications like perforation, mass formation etc. Cases: We present here 6 cases of acute surgical abdomen, with pre-operative diagnosis of right il
Externí odkaz:
https://doaj.org/article/aa05edf2fafd47c78a1ae0c5eec6eb26
Autor:
Tanmay Motiwala, Arvind Sinha, Kirtikumar J Rathod, Vivek Manchanda, Taruna Yadav, Avinash Jadhav, Manish Pathak, Rahul Saxena
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 27, Iss 1, Pp 53-59 (2022)
Introduction: Posterior urethral valve (PUV) is life threatening congenital anomaly of urinary tract. Aim of the study was to correlate urethral ratio (UR) and bladder wall thickness (BWT) with cystoscopic findings in PUV patients to assess residual
Externí odkaz:
https://doaj.org/article/6c5654a8e24e4bd4b295a2fdc7e15a27
Autor:
Chhabi Ranu Gupta, Tejal Bhoy, Anup Mohta, Mamta Sengar, Niyaz A Khan, Vivek Manchanda, Parveen Kumar
Publikováno v:
African Journal of Paediatric Surgery, Vol 19, Iss 3, Pp 160-163 (2022)
Introduction: High and intermediate types of anorectal malformations (ARMs) may be managed by either open posterior sagittal anorectoplasty (PSARP) or by laparoscopic-assisted anorectoplasty (LAARP). Most of the literature favours one approach over t
Externí odkaz:
https://doaj.org/article/406af92838ab43afa80d557dec816e49
Publikováno v:
Journal of Neonatal Surgery, Vol 11 (2022)
Background: Esophageal atresia (EA) with distal trachea-esophageal fistula (TEF), the most common variety of EA, is managed by primary end-to-end anastomosis. Recurrent TEF constitutes the most difficult-to-manage complication of the primary repair a
Externí odkaz:
https://doaj.org/article/dd926aeecea14b21b89de9042a1d725f
Publikováno v:
Journal of Neonatal Surgery, Vol 11 (2022)
Background: Carmi syndrome is the name given to the association of congenital pyloric atresia and epidermolysis bullosa. It has a high mortality. Case series: We report 3 neonates with features of multiple skin blisters and a classical X-ray pictur
Externí odkaz:
https://doaj.org/article/224cf90ce3ef44cc80421cc913948663
Publikováno v:
Journal of Neonatal Surgery, Vol 10 (2021)
Background: The anterior abdominal defects, especially gastroschisis and omphalocele have high mortality rates in developing countries. Time to intervene has been hypothesized to be associated with morbidity and mortality. The aim was to determine fa
Externí odkaz:
https://doaj.org/article/7c79dbd8692f4be58445713821709f18
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 7, Iss 6, Pp 1201-1206 (2013)
Spontaneous or idiopathic biliary perforations are an infrequently encountered but an important cause of surgical jaundice in paediatric patients and one of the most common causes of surgical jaundice in infancy. A pre-operative diagnosis with a
Externí odkaz:
https://doaj.org/article/59ef30ae321b4772bf26a22bc7e680c6
Publikováno v:
Journal of Cutaneous and Aesthetic Surgery, Vol 3, Iss 3, Pp 181-183 (2010)
Bronchogenic cysts occur due to the anomalous development of the primitive tracheobronchial tree early in fetal life. They are usually present in middle mediastinum. Rarely, they have been found in other locations. We describe two patients with subcu
Externí odkaz:
https://doaj.org/article/075a95f186fc446d81d5cd474f5390ef