Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Niyaz Ahmed Khan"'
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 27, Iss 4, Pp 387-390 (2022)
Introduction: Prostatic utricles (PUs) are the remnants of Mullerian ducts found in the male posterior urethra. Enlarged symptomatic utricles are known to be associated with hypospadias. There is a dearth of literature defining an enlarged utricle an
Externí odkaz:
https://doaj.org/article/8717d68d3d034544af56d2c998437c27
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 27, Iss 5, Pp 644-647 (2022)
Rhabdomyosarcoma is an aggressive malignant striated muscle neoplasm commonly seen in children involving orbit, paranasal sinuses, cheek, tongue, and rarely upper lip. The anaplastic subtype is further rare and associated with poor prognosis. Herein,
Externí odkaz:
https://doaj.org/article/731edd077bdd470797f5f49d6c81d1a4
Autor:
Amit Kumar, Vipan Bangar, Niyaz Ahmed Khan, Jigar N Patel, Amit Gupta, Partap Singh Yadav, Rajiv Chadha, Subhasis Roy Choudhury
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 27, Iss 2, Pp 185-190 (2022)
Background: In children with anorectal malformations (ARM), the vertical fibres of the striated muscle complex (SMC) are believed to be located within the limits of the anal dimple (AD). Methods: Forty five cases of ARM underwent posterior sagittal a
Externí odkaz:
https://doaj.org/article/fa656a22f3cc448997731ad3c86f6795
Publikováno v:
Annals of Pediatric Surgery, Vol 17, Iss 1, Pp 1-5 (2021)
Abstract Background Mixed cortico-medullary adrenal carcinoma (MCMAC) is an extremely rare entity with scarce literature on its cytomorphology. Case presentation A 2-year-old girl presented with abdominal pain for 3 days and a past history of fever w
Externí odkaz:
https://doaj.org/article/a3a5887ccf224bd7bed8619cec68fa88
Publikováno v:
Medical Mycology Case Reports, Vol 26, Iss , Pp 5-9 (2019)
Mucormycosis is a rare, fatal angioinvasive infection occurring in immunocompromised individuals. Gastrointestinal mucormycosis is rare variety with high mortality rate. We present a case of GI mucormycosis in a 2-year-old male child who presented wi
Externí odkaz:
https://doaj.org/article/77fa79808245471cb562f05741f11a0c
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 26, Iss 6, Pp 401-403 (2021)
Introduction: Incidence of pediatric urolithiasis has increased over the last few decades. Procedures such as extracorporeal short wave lithotripsy, percutaneous nephrolithotripsy, and ureterorenoscopic lithotripsy are not widely available for pediat
Externí odkaz:
https://doaj.org/article/893b7d4e9a934e658f7ad9f5209b7b39
Autor:
Niyaz Ahmed Khan, Nitin Pant, Amit Gupta, Rama Anand, Partap Singh Yadav, Rajiv Chadha, Subhasis Roy Choudhury
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 24, Iss 2, Pp 104-108 (2019)
Background/Purpose: The radiologic investigations of 25 girls with congenital pouch colon (CPC), managed over 17 years, were retrospectively reviewed. In 13 girls who form the study group, the investigations provided information about the anomalous u
Externí odkaz:
https://doaj.org/article/1cbb6ae21ced4c79a7020913ee116654
Autor:
Muffazzal Rassiwala, Partap Singh Yadav, Subhasis Roy Choudhury, Niyaz Ahmed Khan, Shalu Shah, Pinaki Ranjan Debnath, Rajiv Chadha
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 24, Iss 4, Pp 281-284 (2019)
Aim: This study was aimed at prediction of the gap length between the two esophageal ends in cases of esophageal atresia and distal tracheoesophageal fistula (EA-TEF) by preoperative radiography with a nasogastric tube in the upper esophagus and its
Externí odkaz:
https://doaj.org/article/b1bf315b90314295bd63234c0ceddb4f
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 20, Iss 2, Pp 145-147 (2019)
Kasabach–Merritt phenomenon (KMP) is a severe thrombocytopenic coagulopathy which usually occurs in the presence of enlarging vascular tumors such as kaposiform hemangioendothelioma (KHE) and tufted angioma. The treatment for this potentially fatal
Externí odkaz:
https://doaj.org/article/edea64eb6f844a89aee58ab888158b7e
Autor:
Rajiv Chadha, Niyaz Ahmed Khan
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 22, Iss 2, Pp 69-78 (2017)
Congenital pouch colon (CPC) is an unusual abnormality in which a pouch-like dilatation of a shortened colon is associated with an anorectal malformation. It is categorized into four subtypes (Types I–IV) based on the length of normal colon proxima
Externí odkaz:
https://doaj.org/article/4bd6d4078e2b4f018735857cd4ed13dd