Matozaki T, Sakamoto C, Suzuki T, Chujo S, Matsuda K, Wada K, Nakano O, Konda Y, Nishizaki H, Nagao M
Second Department of Internal Medicine, Kobe University School of Medicine, Japan.
Dig Dis Sci. 1993 May;38(5):963-7. doi: 10.1007/BF01295929.
We present a case of a 27-year-old female suffering from chronic calcifying pancreatitis with diabetes mellitus. Radiographic examinations and exocrine pancreatic function tests revealed considerable dilatation of pancreatic ducts with large intraductal calculi and exocrine pancreatic insufficiency, respectively. Recent literature indicates that a decrease in the activity of pancreatic stone protein (PSP), which inhibits CaCO3 crystal formation in pancreatic juice, is closely related to the development of chronic calcifying pancreatitis. The patient had no apparent cause or family history of pancreatitis. We therefore investigated the possibility that alterations in the PSP gene might explain the chronic pancreatitis seen in this patient. Six exons of the PSP gene amplified by polymerase chain reaction were directly sequenced, but there was no apparent base mutation observed. Furthermore, Southern blot analysis revealed neither rearrangement nor deletion of the PSP gene in the genomic DNA of this case. However, this genetic approach will be useful for future study of the etiology of hereditary pancreatitis.
我们报告一例27岁患有慢性钙化性胰腺炎合并糖尿病的女性病例。影像学检查和胰腺外分泌功能测试分别显示胰管显著扩张伴大量导管内结石以及胰腺外分泌功能不全。近期文献表明,抑制胰液中碳酸钙晶体形成的胰石蛋白(PSP)活性降低与慢性钙化性胰腺炎的发生密切相关。该患者无明显的胰腺炎病因或家族史。因此,我们研究了PSP基因改变可能解释该患者慢性胰腺炎的可能性。通过聚合酶链反应扩增的PSP基因的六个外显子进行直接测序,但未观察到明显的碱基突变。此外,Southern印迹分析显示该病例的基因组DNA中PSP基因既无重排也无缺失。然而,这种基因方法将有助于未来对遗传性胰腺炎病因的研究。