Výsledky vyhledávání - "Fusiform dilatation"

Enfermedad de Caroli: revisión sistemática de la literatura

Autor: Bryan Felipe Vacca Carvajal, Ledmar Jovanny Vargas Rodríguez, María Gabriela Rangel Pereira, José Mario Vasquez Iles

Publikováno v: Revista colombiana de Gastroenterología. 36:180-190

Introducción: la enfermedad de Caroli es un trastorno congénito poco usual, el cual cursa con dilatación segmentaria multifocal de los conductos biliares intrahepáticos. Fue descrita por Jacques Caroli en 1958 como una dilatación sacular, segmen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::01ee2cea0f02d312900ebc8cdd94d469
https://doi.org/10.22516/25007440.612

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Long-term stability of fusiform dilatation of the internal carotid artery following surgery adjacent to the circle of Willis: report of 2 cases

Autor: Madeline B Karsten, R. Michael Scott

Publikováno v: Journal of Neurosurgery: Pediatrics. 27:185-188

Fusiform dilatation of the internal carotid artery (FDCA) is a known postoperative imaging finding after craniopharyngioma resection. FDCA has also been reported following surgery for other lesions in the suprasellar region in pediatric patients and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::88871ff4bd5c4bbbc02479ea1588270f
https://doi.org/10.3171/2020.7.peds20469

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Akademický článek

Innominate Artery Aneurysm: Simulating a Thyroid Nodule

Autor: K. Felix Jebasingh, Dukhabandhu Naik, Anuradha Chandramohan, Rahul Thampi, Nihal Thomas

Publikováno v: Journal of Clinical and Diagnostic Research, Vol 9, Iss 10, Pp OJ01-OJ02 (2015)

Externí odkaz: https://doaj.org/article/e279c9772ca145519cfbf00dfa3f929c

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Fusiform Dilatation of the Internal Carotid Artery in Childhood-Onset Craniopharyngioma: A Systematic Review

Autor: Evan Luther, Joshua D. Burks, Turki Elarjani, Robert M. Starke, Sauson Soldozy, Aria M. Jamshidi

Publikováno v: World neurosurgery. 162

Objective Patients with fusiform dilation of the carotid artery (FDCA) following pediatric craniopharyngioma resection typically have a benign clinical course. We reviewed the neurosurgical literature for FDCA outcomes after resection of these tumors

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43c288830123ea55d0ea2a414104b1cc
https://pubmed.ncbi.nlm.nih.gov/34555575

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Akademický článek

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Type C Pancreaticobiliary Maljunction Is Associated With Perforated Choledochal Cyst in Children

Autor: Jiangbin Liu, Zhibao Lv, Weijue Xu, Jing Xiong, Xiong Huang, Linlin Zhu

Publikováno v: Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 8 (2020)

Background: Perforation of a choledochal cyst (CC) is not rare, but the pathogenesis of spontaneous perforation has not been established. Pancreaticobiliary maljunction (PBM) is commonly seen in association with choledochal cyst. To explore the relat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88649bab7d4dd9cb4b5303ebc2985c84
https://doi.org/10.3389/fped.2020.00168

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A rare case of choledochal cyst presented as sudden and severe abdominal pain

Autor: Lung-Huang Lin

Publikováno v: Journal of Medical Ultrasound
Journal of Medical Ultrasound, Vol 28, Iss 4, Pp 256-259 (2020)

We report a pediatric case of Type 1C choledochal cyst presented as acute biliary colic pain. Choledochal cyst is an abnormal expansion of the biliary tract. The Type 1 choledochal cyst is the cystic dilation of the common bile duct. The Type Ic chol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c81f6a455f81ef28bbf838231f037d10
https://doi.org/10.4103/jmu.jmu_27_20

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Prenatal MR imaging features of Caroli syndrome in association with autosomal recessive polycystic kidney disease

Autor: N. Scott Adzick, Teresa Victoria, Amanda Rivas, Monica Epelman, Enrico Danzer

Publikováno v: Radiology Case Reports
Radiology Case Reports, Vol 14, Iss 2, Pp 265-268 (2019)

Caroli syndrome, which is characterized by saccular and fusiform dilatation of the biliary ducts, is usually observed in association with autosomal recessive polycystic kidney disease (ARPKD). Although the diagnosis of ARPKD is generally easy to make

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e949fc12cbe61c34f04dc3cef6a63d3
http://europepmc.org/articles/PMC6260464

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Akademický článek

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UNILATERAL RENAL AGENESIS AND PROXIMAL BLIND-ENDING URETER WITH URETERIC ATRESIA

Autor: Dilip Kumar Pal, Ritesh Satardey, Krishnendu Maity

Publikováno v: Indian Journal of Case Reports. :344-345

Renal agenesis associated with proximal blind-ending ureter, ureteric atresia, and fusiform dilatation of distal ureter which is an extremely rare occurrence and has not been described in the literature. We report a case of unilateral renal agenesis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a9d060fd0843af88dd4902e25faa099a
https://doi.org/10.32677/ijcr.2020.v06.i06.020

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