Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Safi Nassan"'
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 57, Iss , Pp - (2020)
Background: Insulinoma typically has non-specific neuroglycopenic symptoms. It is a neuroendocrine tumor of the pancreas, and leads to recurring hypoglycemic attacks stemming from insulin hypersecretion. Purpose: We report the case of an 8-year-old b
Externí odkaz:
https://doaj.org/article/26076f7f4f37484db8fbce1f18b62a85
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 54, Iss , Pp - (2020)
Externí odkaz:
https://doaj.org/article/d8b4f91867da4232810a6153244bd0ba
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 28, Iss , Pp 33-36 (2018)
Giant juvenile fibroadenomas are rare variants of fibroadenoma, usually occurring in girls between the ages of 10 and 18 years. They are characterized by massive and rapid enlargement of a rubbery, mobile, and non-tender mass. The etiology is not wel
Externí odkaz:
https://doaj.org/article/f048bf007e654b9f9c77e8d61705cd9c
Publikováno v:
Cureus
Abdominal pain is a common symptom in surgical practice. Around 11%-45% of pediatric population present with abdominal pain. In 29%-87.5% of pediatric population diagnosed with primary hyperparathyroidism (PHPT), abdominal pain and other gastrointest
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 57, Iss, Pp-(2020)
Background Insulinoma typically has non-specific neuroglycopenic symptoms. It is a neuroendocrine tumor of the pancreas, and leads to recurring hypoglycemic attacks stemming from insulin hypersecretion. Purpose We report the case of an 8-year-old boy
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 54, Iss, Pp-(2020)
Autor:
Safi Nassan Ali, Khalid Rasheed, Yasmin Yousef, Saif Abdulghani Alghamdi, Abdullah Ghouth Ali
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 28, Iss, Pp 33-36 (2018)
Giant juvenile fibroadenomas are rare variants of fibroadenoma, usually occurring in girls between the ages of 10 and 18 years. They are characterized by massive and rapid enlargement of a rubbery, mobile, and non-tender mass. The etiology is not wel
Publikováno v:
Cureus
Pancreatoblastoma (PB) is a rare pancreatic neoplasm which arises when a group of pancreatic cells start to go through uncontrollable growth. The diagnosis of PB is challenging due to its vague symptoms. The initial diagnosis is made by imaging, afte
Publikováno v:
In Journal of Pediatric Surgery Case Reports January 2018 28:33-36
Publikováno v:
Annals of Pediatric Surgery; Vol 10, No 1 (2014); 25-26
Splenogonadal fusion is a rare congenital anomaly in which there is fusion of the spleen and the gonad. This report describes a 25-month-old male child who presented with left scrotal swelling. On exploration, a discontinuous type of splenogonadal fu