Anatomical variations of cystic duct (CD) are frequently unrecognized. It is important to be aware of these variations prior to any surgical, percutaneous, or endoscopic intervention procedures. Objectives. The purpose of our study was to demonstrate the imaging features of CD and its variants ...
Zajko AB, Bennett MJ, Campbell WL et al (1990) Mucocele of the cystic duct remnant in eight liver transplant recipients: findings at cholangiography, CT and US. Radiology 177:691–693 PubMed CAS Google Scholar Abcarian PW, Emond JC, Ring EJ (1994) Cystic duct remnant mucocele in a liv...
Mucinous pancreatic duct ectasia in the body of the pancreas. Radiology 1989;170:815–816. 53 Yanagisawa A, Ohashi K, Hori M, et al. Ductectatic- type mucinous cystadenoma and cystadenocarcino- ma of the human pancreas: a novel clinicopathologi- cal entity. Jpn J Cancer Res 1993;84:...
. Usually the proliferation of fibrous tissue occurs and accompaniesepithelial hyperplasia. Many histologic variants of fibrocystic change have been described, including cysts (from microscopic to large, blue, domed cysts), adenosis (florid and sclerosing), fibrosis (periductal and stromal), duct...
KatsuyoshiIto, ...NaofumiMatsunaga, inEuropean Journal of Radiology, 2001 Mucinouscystic neoplasms, sometimes referred to as macrocysticadenomaand macrocysticadenocarcinoma, comprise a spectrum of malignant and premalignant neoplastic conditions of the pancreas.Mucinous cystic neoplasmsare most often located ...
MCN is usually considered to have no communication with intrahepatic duct, but in this particular case, the communication with the biliary duct was suggested from its early stage of the lesion, which would be the cause of peculiar chronological change in MR appearance. This is a preview of ...
This is to evaluate for the presence of an underlying malignancy, which may be the cause of the lymphatic or duct obstruction that preceded abscess formation. Rarely, inflammatory breast cancer can result in the development of malignant breast abscesses and a punch biopsy may be n...
Analysis Variants of the CFTR Gene in Iranian Cystic Fibrosis Patients Background: Cystic fibrosis (CF) is known as one of the most common autosomal recessive disorders, which is caused by mucosal glands. A deficiency in the c... HN Farahzadi,M Akbari - 《Journal of Human Genetics & Genomi...
Cystic fibrosis is caused by different mutations in theCFTRgene and can vary in severity and manifestation. Besides the well-known pulmonary consequences, the hepatobiliary and gastrointestinal tracts are also involved and will be the focus of this Revie
lesions and included: absence of fibrosis, acinar parenchyma occupying >95% of the pancreas tissue area, absence of duct-like structures, and absence of pancreatic duct dilation. CFTR mutation analysis Genotyping for CFTR mutations was done via a multiplex assay to screen for 159 CFTR variants ...