Exceptional Mirizzi syndrome in a young child: A laparoscopic approach

Prada-Arias, Marcos; Vázquez-Castelo, José Luis; Blanco-Lobato, Patricia; Gómez-Veiras, Javier; Montero-Sánchez, Margarita; Vieito-Fuentes, Juan Manuel

doi:10.1016/j.epsc.2014.09.001

Cited by 3 publications

(2 citation statements)

References 14 publications

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“…5,6 En niños y adolescentes, los pocos estudios publicados refieren a la obesidad como el principal factor predisponente, seguido de edades entre tres y 15 años, sexo masculino y tener duplicación o anomalías morfológicas del conducto biliar. [7][8][9] En nuestro paciente se cumplieron los tres primeros.…”

Section: Discussionunclassified

Síndrome de Mirizzi asociado a coledocolitiasis

Velasco-Castro,

Sánchez-Gamboa,

García-Agudelo

et al. 2023

Revista Mexicana De Pediatría

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Introducción: el síndrome de Mirizzi (SM) es una complicación poco frecuente en colecistitis y colelitiasis, caracterizada por la presencia de un cálculo biliar grande o de múltiples cálculos en el conducto cístico; lo cual se asocia a inflamación, obstrucción externa de la vía biliar, con o sin fístula colecistocoledocal. Caso clínico: adolescente de 14 años, con obesidad y sintomatología compatible con obstrucción de la vía biliar. Los estudios de colangio-pancreatografía retrógrada endoscópica y colangiorresonancia magnética nuclear apoyaron el diagnóstico de SM. Se realizó colecistectomía laparoscópica de manera exitosa. Conclusiones: el SM es una entidad rara que se debe considerar en el diagnóstico diferencial de la ictericia colestásica en adolescentes con sobrepeso u obesidad.

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Section: Discussionunclassified

Síndrome de Mirizzi asociado a coledocolitiasis

Velasco-Castro,

Sánchez-Gamboa,

García-Agudelo

et al. 2023

Revista Mexicana De Pediatría

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“…However, in operations without confirmed preoperative diagnosis such as Mirizzi syndrome, this risk goes up to 17% [4]. Intraoperative cholangiography and ultrasound can be used to confirm the diagnosis or to determine the presence and extent of biliary fistula.…”

Section: Discussionmentioning

confidence: 99%

Minimally Invasive Treatment of Mirizzi Syndrome, a Rare Cause of Cholestasis in Childhood

Tuncer

Yılmaz

Yavuz

et al. 2016

Case Reports in Pediatrics

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Mirizzi syndrome is the compressive blockage of the cystic or choledochal duct caused by a biliary stone occupying the cystic canal or Hartmann's pouch. This occurrence is rare and, in English literature, three cases defined in children have been observed. In order to draw attention to this rare occurrence, we preferred a 14-year-old male patient with Mirizzi syndrome. In this case, ERCP was performed preoperatively and the diagnosis was carried out with the help of clear visualisation and identification of the tissue structures as well as the stent placed in bile duct; so we protected the patient from the possible iatrogenic injury occurring during surgery.

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Furosemide

2016

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Exceptional Mirizzi syndrome in a young child: A laparoscopic approach

Cited by 3 publications

References 14 publications

Síndrome de Mirizzi asociado a coledocolitiasis

Síndrome de Mirizzi asociado a coledocolitiasis

Minimally Invasive Treatment of Mirizzi Syndrome, a Rare Cause of Cholestasis in Childhood

Furosemide

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