Complete obstruction of the lower common bile duct caused by autoimmune pancreatitis: is biliary reconstruction really necessary?

Toshiki Matsubara, Yoichi Sakurai, Hirotake Miura, Hidetaka Kobayashi, Mitsutaka Shoji, Yasuko Nakamura, Hiroki Imazu, Shigeru Hasegawa, Masahiro Ochiai, Takahiko Funabiki
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引用次数: 10

Abstract

Recent observations suggest that an immune response is involved in the development of chronic pancreatitis. We report a case of autoimmune pancreatitis in a patient who showed complete obstruction of the lower common bile duct. A 63-year-old man was admitted to a local hospital, complaining of appetite loss and back pain. The patient had obstructive jaundice, and percutaneous transhepatic gallbladder drainage was performed. Fluorography through the biliary drainage catheter showed complete obstruction of the lower common bile duct. The patient had no history of alcohol consumption and no family history of pancreatic disease. Physical examination revealed an elastic hard mass palpable in the upper abdomen. Abdominal ultrasound and abdominal computed tomography (CT) scans showed enlargement of the pancreas head. While autoimmune pancreatitis was highly likely, due to the patient's high serum immunoglobulin level, the possibility of carcinoma of the pancreas and/or lower common bile duct could not be ruled out. Laparotomy was performed, and wedge biopsy samples from the pancreas head and body revealed severe chronic pancreatitis with infiltration of reactive lymphocytes, a finding which was compatible with autoimmune pancreatitis. Cholecystectomy and biliary reconstruction, using choledochojejunostomy, were performed, because the complete bile duct obstruction was considered to be irreversible, due to severe fibrosis. After the operation, prednisolone (30 mg/day) was given orally for 1 month, and the entire pancreas regressed to a normal size. Complete obstruction of the common bile duct caused by autoimmune pancreatitis has not been reported previously; this phenomenon provides an insight into autoimmune pancreatitis and provokes a controversy regarding whether biliary reconstruction is needed for the treatment of complete biliary obstruction caused by autoimmune pancreatitis.

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自身免疫性胰腺炎引起的胆总管下段完全梗阻:胆道重建真的有必要吗?
最近的观察表明,免疫反应参与慢性胰腺炎的发展。我们报告一例自身免疫性胰腺炎患者表现为胆总管下段完全梗阻。一名63岁的男子因食欲不振和背部疼痛被当地一家医院收治。患者为梗阻性黄疸,行经皮肝胆囊引流术。胆道引流管造影显示胆总管下段完全梗阻。患者无饮酒史,无胰腺疾病家族史。体格检查显示在上腹部可触及一弹性硬块。腹部超音波及腹部电脑断层扫描显示胰头肿大。虽然自身免疫性胰腺炎的可能性很大,但由于患者血清免疫球蛋白水平较高,不能排除胰腺癌和/或胆总管下段癌的可能性。进行剖腹手术,胰腺头部和胰腺体的楔形活检显示严重的慢性胰腺炎伴反应性淋巴细胞浸润,这一发现与自身免疫性胰腺炎相一致。由于胆管梗阻严重纤维化,被认为是不可逆的,因此采用胆总管空肠吻合术进行胆囊切除术和胆道重建。术后给予强的松龙(30 mg/天)口服1个月,整个胰腺恢复正常大小。自身免疫性胰腺炎引起的胆总管完全梗阻此前未见报道;这一现象为自身免疫性胰腺炎的研究提供了新的视角,也引发了关于自身免疫性胰腺炎引起的完全性胆道梗阻是否需要胆道重建的争议。
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