Histological and immunohistochemical study of an unusual type of gallbladder duplication.
Carriel,José Aneiros-Fernández,Ruyffelaert M,Salvador Arias-Santiago,Riady,Izquierdo-Martínez F,Olga Roda,Maria Cornelissen,A. Campos,Miguel Alaminos +9 more
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TLDR
In presence of an atypical imaging of the gallbladder, diagnosis of this group of congenital anomalies should be considered in order to adequately plan surgical intervention if necessary.Abstract:
Gallbladder duplication is a rare congenital anomaly, with an incidence of 1 in 3,800 autopsies. The correct diagnosis and treatment of this type of entity is important in clinical practice, because it may cause some clinical and surgical problems. In this report, we present the clinical case of a 28-year-old female with abdominal pain. Ultrasound of the upper abdomen showed a distended gallbladder with the presence of a septum that could suggest a congenital anomaly of the extrahepatic biliary system. During surgery, a distended and inflamed gallbladder with a lithiasis was found. In addition, a complete septum and double cystic duct were observed. The gross and histopathological evaluation of the surgical specimen allowed us to confirm the diagnosis of a Y- shaped type gallbladder duplication according to Boyden�s classification. In conclusion, in presence of an atypical imaging of the gallbladder, diagnosis of this group of congenital anomalies should be considered in order to adequately plan surgical intervention if necessaryread more
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Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia.
Francisco Bermúdez-Jiménez,Víctor Carriel,Andreas Brodehl,Miguel Alaminos,Antonio Campos,Ilona Schirmer,Hendrik Milting,Beatriz Álvarez Abril,Miguel Álvarez,Silvia López-Fernández,Diego García-Giustiniani,Lorenzo Monserrat,Luis Tercedor,Juan Jiménez-Jáimez +13 more
TL;DR: The novel DES-p.Glu401Asp mutation causes predominant inherited left ventricular arrhythmogenic cardiomyopathy/dysplasia with a high incidence of adverse clinical events in the absence of skeletal myopathy or conduction system disorders.
Journal ArticleDOI
In vitro characterization of a nanostructured fibrin agarose bio-artificial nerve substitute.
Víctor Carriel,Víctor Carriel,Giuseppe Scionti,Fernando Campos,Olga Roda,Begoña Castro,Maria Cornelissen,Ingrid Garzón,Miguel Alaminos +8 more
TL;DR: It is demonstrated that it is possible to generate biologically active and mechanically stable tissue‐like substitutes with specific dimensions, based on the use of HADMSCs, FAHs and a nanostructure technique.
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Coexistence of double gallbladder with cholangiocarcinoma: A case report.
Wei Chen,Ruoling Han +1 more
TL;DR: The first reported case with coexistence of gallbladder duplication and cholangiocarcinoma, which was diagnosed by abdominal ultrasound, CT and MRCP, as well as further confirmed in surgery and pathology, emphasized the importance of a thorough examination ofgallbladder before surgery.
References
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The accessory gall‐bladder– an embryological and comparative study of aberrant biliary vesicles occurring in man and the domestic mammals
Book
Histology for pathologists
TL;DR: The new edition of Histology for Pathologists will update the pathologist's understanding of normal histology up to date with the incremental advances made in the last five years.
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Combination of fibrin-agarose hydrogels and adipose-derived mesenchymal stem cells for peripheral nerve regeneration
Víctor Carriel,Juan Garrido-Gómez,Pedro Hernández-Cortés,Ingrid Garzón,Salomé García-García,José Antonio Sáez-Moreno,María del Carmen Sánchez-Quevedo,Antonio Campos,Miguel Alaminos +8 more
TL;DR: Clinical, electrophysiological and histological improvements obtained with tissue-engineered ADMSC conduits may contribute to enhancing axonal regeneration by Schwann cells.
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Anatomical variations of the extrahepatic biliary tree: review of the world literature.
TL;DR: The world literature on congenital variation of extrahepatic biliary anatomy is reviewed, as the literature abounds with reports of specific anatomical variations, and their operative implications.