2012
DOI: 10.1016/j.gastrohep.2012.03.012
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Ascitis quilosa posquirúrgica en un adulto tratada con octreótida

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Cited by 4 publications
(10 citation statements)
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“…In our case, after analyzing the sample, a triglyceride value of 357 mg/dl was obtained, which confirmed the diagnosis. It is a rare entity whose incidence varies depending on the literature that we consulted: 1 case for every 11,500 to 80,000 patients [5][6][7]. Its pathophysiology is explained as a disruption of the lymphatic system due to a traumatic injury or an obstruction of lymphovenous or lympho-lymphatic communications [6].…”
Section: Discussionmentioning
confidence: 99%
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“…In our case, after analyzing the sample, a triglyceride value of 357 mg/dl was obtained, which confirmed the diagnosis. It is a rare entity whose incidence varies depending on the literature that we consulted: 1 case for every 11,500 to 80,000 patients [5][6][7]. Its pathophysiology is explained as a disruption of the lymphatic system due to a traumatic injury or an obstruction of lymphovenous or lympho-lymphatic communications [6].…”
Section: Discussionmentioning
confidence: 99%
“…The presence of triglyceride concentrations above 200 mg/dl in the ascitic fluid analysis confirms the diagnosis [2][3][4]. According to the literature consulted [5][6][7], it is a rare finding with an incidence of 1/11,500-80,000 patients.…”
Section: Introductionmentioning
confidence: 99%
“…Una vez definido el tipo de ascitis (ver Figura 1 y 2), el tratamiento óptimo de la AQ depende de la etiología subyacente [10,15,20,25] . Se incluyen medidas dietéticas, uso de agentes farmacológicos e intervenciones percutáneas o quirúrgicas, y deben estar orientadas a lograr alivio sintomático, y en tratar la causa que provoca la AQ (6).…”
Section: Discussionunclassified
“…En caso no haya mejoría, se sugiere el uso de agentes farmacológicos, como somatostatina, la cual reduce la presión portal al inhibir el glucagón y la vasodilatación mediada por otros péptidos intestinales esplácnicos, y se administra por vía endovenosa; octeótride, un análogo de la somatostatina [15,16] , que por su vida media más prolongada se puede administrar por vía subcutánea [7] , y actúa de forma indirecta, inhibiendo las hormonas vasodilatadoras intestinales, y de forma directa, inhibiendo la excreción de líquido linfático, vía canales de calcio, inhibiendo los receptores de somatostatina tipo2 de la pared de vasos linfáticos intestinales [22,25] . Puede darse a dosis inicial de 100ug cada 8 horas por vía subcutánea, en caso de no mejoría, puede incrementarse hasta 250ug cada 8 horas [22] .…”
Section: Discussionunclassified
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