Complete dorsal pancreatic agenesis and unilateral renal agenesis
نویسندگان
چکیده
منابع مشابه
Complete dorsal pancreatic agenesis and unilateral renal agenesis
Dorsal pancreatic agenesis is a very rare congenital anomaly. Unilateral renal agenesis, on the other hand, is a relatively common congenital anomaly, although its etiology is not fully understood. Renal and pancreatic embryologic development appears to be nonrelated. We report a case of a 34-year-old man who was referred to our hospital for evaluation of cholestasis and microalbuminuria. Ultra...
متن کاملDorsal pancreatic agenesis.
CONTEXT Agenesis of the dorsal pancreas is a rare entity and might present with various symptoms. We report a case which presented with chronic pancreatitis. CASE REPORT The patient presented with epigastric pain and we found dorsal pancreatic agenesis causing chronic pancreatitis. CONCLUSIONS Dorsal pancreatic agenesis can be easily diagnosed with new techniques and its association with cl...
متن کاملIsolated Dorsal Pancreatic Agenesis.
Developmental anomalies of the pancreas have been reported; but among these, agenesis of dorsal pancreas is an extremely rare congenital pancreatic anomaly. It may be asymptomatic and incidentally detected on imaging or may be associated with diabetes mellitus or attacks of pancreatitis. We report a rare case of agenesis of dorsal pancreas that was detected incidentally on imaging and there was...
متن کاملDorsal pancreatic agenesis: description of CT signs.
To cite: Sandip S, Chandrashekhara SH, Khandelwal RK, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015210093 DESCRIPTION Agenesis of the dorsal pancreas is rare and is characterised by the absence of the body and tail of the pancreas. Patients with agenesis of the dorsal pancreas often present with non-specific abdominal symptoms and very often it is an...
متن کاملMeckel-Gruber Syndrome with unilateral renal agenesis.
Meckel-Gruber Syndrome (MKS) is an autosomal recessive disorder, characterized by a combination of central nervous system malformation (occipital encephalocele), post-axial polydactyly, and enlarged polycystic kidney dysplasia. With a recurrence risk of 25% this lethal syndrome can be detected in early screening by ultrasound. However, to the authors' knowledge, association of MKS with unilater...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Radiology Case Reports
سال: 2018
ISSN: 1930-0433
DOI: 10.1016/j.radcr.2017.10.025