Introduction Interstitial ectopic pregnancy is a rare and potentially life‐threatening condition that occurs when a fertilized ovum implants in the interstitial (intramural) portion of the fallopian tube within the myometrium. It accounts for 2%–4% of all ectopic pregnancies and poses significant risks due to the potential for rupture and severe ...
Nasser Saleh Alabbad +5 more
wiley +1 more source
Radiological Society of North America (RSNA) 3D printing Special Interest Group (SIG): Guidelines for medical 3D printing and appropriateness for clinical scenarios [PDF]
Este número da revista Cadernos de Estudos Sociais estava em organização quando fomos colhidos pela morte do sociólogo Ernesto Laclau. Seu falecimento em 13 de abril de 2014 surpreendeu a todos, e particularmente ao editor Joanildo Burity, que foi seu ...
Burity, Joanildo +2 more
core +2 more sources
Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature
Abernethy malformation, also called as congenital extrahepatic portosystemic venous shunt, is a rare anomaly involving the portal venous system. Although rare, it is increasingly being reported and is important to diagnose given the adverse clinical ...
Sushil Azad +3 more
doaj +1 more source
Congenital vascular malformations update [PDF]
Presently, there is controversy and misconception in the diagnosis and management of most congenital vascular malformations. The aim of this manuscript is to identify the current knowledge of these poorly understood and relatively uncommon pathologies ...
Albores Figueroa, Rosemberg +4 more
core
Nasal Septal Perforation and Hereditary Hemorrhagic Telangiectasia: Evolution in Management
We performed a case series of nine patients with hereditary hemorrhagic telangiectasia complicated by nasal septal perforation, demonstrating evolution in management paradigms over the last two decades. ABSTRACT Objectives To review septal perforation management and outcomes in patients with hereditary hemorrhagic telangiectasia (HHT).
Stephen F. Bansberg +5 more
wiley +1 more source
Massive glosso-cervical arteriovenous malformation: the rationale for a challenging surgical resection [PDF]
Massive arterivenous malformations (AVM) in the cervico-facial area are rare but potentially life-threatening. Treatment protocols are not well-established.
González García, R. +2 more
core +1 more source
Phenotypic Analysis of Embryos in a Noonan Syndrome Model Mouse With the Rit1 A57G Mutation
Rit1A57G/+ embryos exhibited cardiac hypertrophy and lymphatic vessel dilatation. The administration of the MEK1/2 inhibitor ameliorated LV myocardial wall hypertrophy. The MEK/ERK activation would be one of the pathogenetic mechanisms of cardiac hypertrophy of Rit1A57G/+ embryos.
Dai Suzuki +4 more
wiley +1 more source
Imaging Diagnosis of Neonatal Umbilical Arteriovenous Malformation Complicated with Portosystemic Shunt [PDF]
In the last twenty years, there were less than 10 cases of umbilical arteriovenous malformations have been reported, which usually had single complication, included mild cardiac dilatation, pulmonary hypertension, hemorrhagic shock, and hepatic damage ...
Zhang Minyu, Jia Baocheng, Huang Liuming
doaj +1 more source
Percutaneous Embolization of Congenital Portosystemic Venous Fistula in an Infant with Down Syndrome [PDF]
Congenital intrahepatic portosystemic venous shunts are rare vascular malformations often associated with severe complications. We describe a term male infant with Down syndrome with high output heart failure secondary to a congenital arterial to portal ...
Matthew Files +4 more
core +1 more source

