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患有家族性乳糜微粒血症综合征的两兄弟反复出现急性和慢性胰腺炎。

Recurrent acute and chronic pancreatitis in two brothers with familial chylomicronemia syndrome.

作者信息

Truninger Kaspar, Schmid Peter A, Hoffmann Michael M, Bertschinger Philipp, Ammann Rudolf W

机构信息

Clinic of Gastroenterology, University Hospital Berne, CH-3010 Berene, Switzerland.

出版信息

Pancreas. 2006 Mar;32(2):215-9. doi: 10.1097/01.mpa.0000202942.93578.dd.

Abstract

The chylomicronemia syndrome is well recognized as a rare etiologic factor of acute pancreatitis; however, whether hypertriglyceridemia can cause chronic pancreatitis (CP) remains unclear. We describe the long-time course of 2 brothers with the familial chylomicronemia syndrome caused by identical compound heterozygous mutations in the lipoprotein lipase (LPL) gene with markedly reduced LPL activity. Other etiologic factors were excluded, including mutations in the PRSS1, SPINK1, and CFTR gene. Although both brothers had recurrent acute pancreatitis and the same LPL genotype, CP became evident in only one patient. Progression to CP was associated with a more severe disease course. Thus, the chylomicronemia syndrome may cause CP in the absence of other known causative factors, and similar to alcoholic and hereditary CP, a more severe disease course is associated with disease progression.

摘要

乳糜微粒血症综合征是急性胰腺炎一种公认的罕见病因;然而,高甘油三酯血症是否会导致慢性胰腺炎(CP)仍不清楚。我们描述了2名患有家族性乳糜微粒血症综合征兄弟的长期病程,他们因脂蛋白脂肪酶(LPL)基因相同的复合杂合突变导致LPL活性显著降低。其他病因已被排除,包括PRSS1、SPINK1和CFTR基因的突变。尽管两兄弟均有复发性急性胰腺炎且LPL基因型相同,但只有一名患者出现了明显的CP。疾病进展为CP与更严重的病程相关。因此,在没有其他已知致病因素的情况下,乳糜微粒血症综合征可能会导致CP,并且与酒精性和遗传性CP相似,更严重的病程与疾病进展相关。

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