Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Satish P Kapadnis"'
Autor:
Sandesh V Parelkar, Satish P Kapadnis, Beejal V Sanghvi, Prashant B Joshi, Dinesh Mundada, Shishira Shetty, Sanjay N Oak
Publikováno v:
African Journal of Paediatric Surgery, Vol 11, Iss 4, Pp 362-365 (2014)
Pyloric atresia (PA) is a rare congenital anomaly that constitutes approximately 1% of all intestinal atresias, and its incidence is approximately 1 in 100,000 live births. PA may occur as an isolated condition or associated with other abnormalities,
Externí odkaz:
https://doaj.org/article/13d428e8928c4bcb8ce7957de83b1296
Autor:
Sandesh V Parelkar, Pooja V Multani, Beejal V Sanghvi, Shishira R Shetty, Hemangi R Athawale, Satish P Kapadnis, Dinesh D Mundada, Sanjay N Oak
Publikováno v:
Journal of Minimal Access Surgery, Vol 9, Iss 4, Pp 159-162 (2013)
Background: The incidence of hypertrophic pyloric stenosis is approximately 1-3 per 1,000 live births. Hypertrophic pyloric stenosis is seen more often in males, with a male-to female ratio of 4:1. Laparoscopic pyloromyotomy is becoming increasingly
Externí odkaz:
https://doaj.org/article/ba43d461161440f3b78cc4a6e7465fd0
Autor:
Sandesh V Parelkar, Sanjay N Oak, Satish P Kapadnis, Beejal V Sanghvi, Prashant B Joshi, Pragati Sathe, Dinesh Mundada, Shishira Shetty
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 18, Iss 1, Pp 38-40 (2013)
An 11-year-old girl with a pancreatic solid pseudo papillary tumor (SPT) is reported. Contrast enhanced computerized tomography (CECT) & Magnetic resonant imaging (MRI) abdomen revealed a well-defined inhomogenous mass arising from the retro-peritone
Externí odkaz:
https://doaj.org/article/e74d58b7500c4e7e8b8c48f73623822d
Autor:
Sanjay N Oak, Dinesh Mundada, Satish P. Kapadnis, Sandesh V. Parelkar, Prashant B Joshi, Beejal V Sanghvi
Publikováno v:
Pediatrics and Neonatology, Vol 57, Iss 3, Pp 232-235 (2016)
Gastrointestinal perforation in neonates with anorectal malformation (ARM) is extremely uncommon. Delayed patient presentation is an important causative factor. A 2.5-kg neonate presented 72 hours after birth with abdominal distention and absent anal
Autor:
Sandesh V. Parelkar, Prashant B Joshi, Satish P. Kapadnis, Sanjay N Oak, Beejal V Sanghvi, Dinesh Mundada
Publikováno v:
Journal of Pediatric Neurosciences
Meckel-Gruber syndrome is a rare autosomal recessive lethal malformation characterized by typical manifestations of occipital encephalocele, bilateral polycystic kidneys and post axial polydactyly. The worldwide incidence varies from 1 in 13,250 to 1
Autor:
Prashant B Joshi, Dinesh Mundada, Beejal V Sanghvi, Sandesh V. Parelkar, Shishira Shetty, Satish P. Kapadnis, Sanjay N Oak
Publikováno v:
The Annals of The Royal College of Surgeons of England. 95:e3-e5
Lipomas are the most commonly encountered benign mesenchymal tumour, arising in any location where fat is normally present. Lipomas in the head and neck are rare in all age groups. Cases of vascular sheath lipomas in the femoral region have only been
Autor:
Prashant B Joshi, Beejal V Sanghvi, Dinesh Mundada, Sandesh V. Parelkar, Satish P. Kapadnis, Sanjay N Oak, D. K. Kulkarni
Intracaval tumor extension is reported in 4 % to 10 % of cases, mostly into the infrahepatic portion. However it may rarely extend into the right atrium (1.4 %) [1]. The management of tumors that extend into the inferior vena cava is determined by ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::667c999a9ca337a36fb6c1ea54b2d805
https://europepmc.org/articles/PMC3890013/
https://europepmc.org/articles/PMC3890013/
Autor:
Dinesh Mundada, Shishira Shetty, Prashant B Joshi, Satish P. Kapadnis, Sanjay N Oak, Beejal V Sanghvi, Sandesh V. Parelkar
Publikováno v:
Journal of pediatric surgery. 47(10)
Meningomyelocele (MMC) is very rarely associated with teratoma. Only few reports on the concurrence of a teratoma within a meningomyelocele have been published. The hypotheses of a possible common aetiology for this association include a single dysem
Autor:
Hemangi R. Athawale, Beejal V Sanghvi, Satish P. Kapadnis, Sanjay Oak, Dinesh Mundada, Sandesh V. Parelkar, Pooja Multani, Shishira Shetty
Publikováno v:
Journal of Minimal Access Surgery
Journal of Minimal Access Surgery, Vol 9, Iss 4, Pp 159-162 (2013)
Journal of Minimal Access Surgery, Vol 9, Iss 4, Pp 159-162 (2013)
Background: The incidence of hypertrophic pyloric stenosis is approximately 1-3 per 1,000 live births. Hypertrophic pyloric stenosis is seen more often in males, with a male-to female ratio of 4:1. Laparoscopic pyloromyotomy is becoming increasingly
Autor:
Dinesh Mundada, Satish P. Kapadnis
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 3, Iss 2, Pp 72-74 (2015)
A wide variety of anomalies may occur as a result of the vitellointestinal duct (VID) failing to obliterate completely. VID is well known because of its various complication and presentation most commonly due to Meckel's diverticulum. Small bowel pro