Zobrazeno 1 - 10
of 116
pro vyhledávání: '"Paras kothari"'
Publikováno v:
Urology Case Reports, Vol 52, Iss , Pp 102643- (2024)
Exstrophy variants are uncommon developmental anomalies, with the inferior vesical variant being the rarest among them. We present the case of a 1-year-old continent boy with an inferior vesical fistula (IVF) with solitary kidney and ureterocele wher
Externí odkaz:
https://doaj.org/article/fb754dbd95504a33ae5907eef220b077
Autor:
Aditi Vijay Dalvi, Maitreyee Save, Paras Kothari, Abhaya Gupta, Sanjay Oak, Shahaji Deshmukh, Apoorva Kulkarni, Saket Jha, Dhvani Shah
Publikováno v:
Urology Case Reports, Vol 51, Iss , Pp 102609- (2023)
Bilateral single system ectopic ureters are a rare entity in paediatric urology. We report a girl child with bilateral single system ectopic ureters with right system opening into the vagina, who presented at 3.5 years with continuous dribbling of ur
Externí odkaz:
https://doaj.org/article/5fc5636685c84b24b42403b50c1fa8db
Autor:
Aditi Vijay Dalvi, Maitreyee Save, Paras Kothari, Abhaya Gupta, Shahaji Deshmukh, Apoorva Kulkarni, Saket Jha, Dhvani Shah
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 89, Iss , Pp 102570- (2023)
Background and aim: Oesophageal duplication is a rare congenital malformation which occurs due to embryogenesis errors. It accounts for 15% of all digestive tract duplications, most common being ileal duplications. Here we report a case of tubular Oe
Externí odkaz:
https://doaj.org/article/b92d1c8d41474f5ca7dafba90fc2b7e1
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 83, Iss , Pp 102268- (2022)
Bilateral synchronous Wilms tumour represents 4–8% of all Wilms tumours (WTs). The ultimate goal in such cases is to preserve as much renal parenchyma as possible while achieving total/near total tumour resection. We report the case of a 3 years ol
Externí odkaz:
https://doaj.org/article/119e6abfcff54b62b40c10d958b78972
Publikováno v:
Journal of Minimal Access Surgery, Vol 17, Iss 1, Pp 88-90 (2021)
Foregut duplication is more common in girls, particularly if there is bronchopulmonary involvement. The incidence of oesophageal duplication cyst is estimated to be one in 8200 live births with male prevalence. Most duplications are benign, but the p
Externí odkaz:
https://doaj.org/article/e18d0fc9680a4a6a8ae865cbd0b36198
Autor:
Aboli Hukeri, Abhaya Gupta, Paras Kothari, Vishesh Dikshit, Geeta Kekre, Prashant Patil, Apoorva Kulkarni, Arjun Pawar
Publikováno v:
Journal of Minimal Access Surgery, Vol 15, Iss 1, Pp 51-55 (2019)
Traditional management of infantile Hypertrophic Pyloric Stenosis is open pyloromyotomy after initial adequate resuscitation of the patient. From 1991, laparoscopic approach is considered feasible and safe. Today, diagnosis of hypertrophic pyloric st
Externí odkaz:
https://doaj.org/article/a2a23d80dc524b33b58211e713bc8ff1
Autor:
Saurabh Jitendra Tiwari, Apoorva Kulkarni, Geeta Kekre, Abhaya Gupta, Shalika Jayaswal, Paras Kothari
Publikováno v:
Journal of Neonatal Surgery, Vol 8, Iss 4 (2020)
Despite advances in antenatal diagnosis and perinatal care, mortality rate remains elevated in patients with congenital diaphragmatic hernia (CDH). We report a case of left sided CDH in a term baby with persistent gastroesophageal reflux (GER) after
Externí odkaz:
https://doaj.org/article/6ac813f1bbd7490f8267268a1fb5a433
Autor:
Paras Kothari, Abhaya Gupta, Prashant S Patil, Geeta Kekre, Ravi Kamble, Kiran Vishesh Dikshit
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 21, Iss 2, Pp 78-80 (2016)
Complete midline sternal cleft is a rare congenital anomaly resulting from failed midline ventral fusion of the sternal bars. Very few cases of complete sternal cleft have been described in literature. We present a case of complete sternal cleft in a
Externí odkaz:
https://doaj.org/article/64182ca4cc074db296be361d1929512c
Autor:
Prashant Sadashiv Patil, Paras Kothari, Abhaya Gupta, Rahul Gupta, Geeta Kekre, Vishesh Dikshit, Ravi Kamble
Publikováno v:
Journal of Neonatal Surgery, Vol 5, Iss 2 (2016)
Cloacal exstrophy is a very rare and complex malformation. We report a neonate of cloacal exstrophy with mature teratoma presenting as a component of exstrophy. To our knowledge this has not been reported in the literature.
Externí odkaz:
https://doaj.org/article/b23ca3526e1148de931102792c529d64
Autor:
Pashant Sadashiv Patil, Paras Kothari, Abhaya Gupta, Geeta Kekre, Vishesh dikshit, Ravi kamble, Kedar Mudkhedkar
Publikováno v:
Journal of Neonatal Surgery, Vol 5, Iss 2 (2016)
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Externí odkaz:
https://doaj.org/article/094db4010c9c48f6a39a0371853f4583