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Preeminence of Lesser Splanchnic BloodFlow in Selected Patients WithGeneralized Portal Hypertension

机译:在部分门脉高压症患者中,内脏血流量较小的优势

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Although restricted transhepatic portal flow is necessary for development of generalized portalhypertension (GPH), increased splanchnic arterial inflow also contributes to GPH and its clinicalsequelae. In this context, we describe 7 male and 6 female patients (mean age 48 years) in whom thelesser splanchnic (gastrosplenic) system played a key role in the signs and symptoms of GPH. These 13patients (9 with hepatic cirrhosis, 3 with primary myeloproliferative disorder, and 1 with extrahepaticportal block) shared common features of massive splenomegaly, huge splenofundic gastric varices, oftenwith a prominent natural shunt to the left renal vein. Total or near total splenectomy alone or combinedwhere appropriate with coronary vein ligation was effective in controlling varix hemorrhage (10patients), ascites (3), or complications of an enlarged spleen-anorexia and abdominal pain (3),hemolytic anemia (1) and profound thrombocytopenia with severe epistaxis (1). Intraoperative jejunalportal venography was crucial in operative management in order to establish definitively the presence orabsence of coronary venous collaterals, and when present, to verify their operative ligation.These distinctive patients illustrate: 1) GPH is a heterogeneous syndrome of divergent splanchniccirculatory patterns, a feature which should be taken into account in selecting operative treatment; 2)one well-defined subgroup displays prominent hyperdynamic lesser splanchnic and specifically, splenicblood flow as a major contributor to clinical complications; and 3) within this subgroup, splenectomycombined with documented absence or surgical interruption of coronary venous collaterals as corroboratedby intraoperative portography is effective alternative treatment.
机译:尽管发展成门静脉高压症(GPH)必须限制肝内门静脉血流,但是内脏动脉血流的增加也有助于GPH及其临床后遗症。在这种情况下,我们描述了7例男性和6例女性患者(平均年龄48岁),其中较小的内脏(胃脾)系统在GPH的体征和症状中起关键作用。这13例患者(肝硬化9例,原发性骨髓增生性疾病3例,肝门外阻滞1例)具有脾大肿大,胃底巨大脾静脉曲张的共同特征,通常左肾静脉自然分流。单独或联合全脾切除术或结合适当的冠状动脉结扎术可有效控制静脉曲张出血(10例患者),腹水(3)或脾脏厌食和腹痛扩大(3),溶血性贫血(1)和严重的并发症患有严重鼻出血的血小板减少症(1)。术中空肠静脉造影对于明确确定冠状静脉侧支的存在与否以及在证实其手术结扎的情况下在手术管理中至关重要。这些独特的患者说明:1)GPH是内脏循环多样的异质综合症,这是特征选择手术治疗时应考虑到这一点; 2)一个明确定义的亚组表现出明显的高动力性小内脏,特别是脾血流量是导致临床并发症的主要因素; 3)在该亚组中,脾切除术结合术中门静脉造影所证实的冠状静脉侧支缺失或手术中断是有效的替代治疗。

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