Bouzid Ahmed, Fendri Sami, Rejab Haitham, Trigui Ayman, Mejdoub Youssef, Boujelbene Salah
Department of General Surgery, Habib Bourguiba Hospital, Sfax, Tunisia.
Ann Med Surg (Lond). 2023 Feb 7;85(3):460-465. doi: 10.1097/MS9.0000000000000186. eCollection 2023 Mar.
Spontaneous perforation of the common bile duct (SPCBD) is an exceptional disease, especially in adults. The cause is often idiopathic once trauma and choledochal cyst are excluded. Early diagnosis is often difficult because of its often-misleading appearance.
The authors report the case of a 54-year-old man, a known case of type 2 diabetes mellitus, who presented to our emergency department for acute abdominal pain that had evolved for 2 days.
On physical examination, the patient had a fever of up to 38.5°C, and the abdomen was distended and generally tight. The abdominal computerized tomography scan confirms the presence of free fluid. In addition, the thickness of the gallbladder wall had increased in contrast with a resolved gallbladder distention. Because exploration failed to demonstrate the cause of ascites, the authors performed a diagnostic paracentesis, which revealing ascites with a dark yellow-green color, which implied bile leakage.After initial resuscitation, an emergent exploratory laparotomy was performed. The authors found biliary peritonitis secondary to SPCBD. After peritoneal lavage, the perforation was repaired over a T-tube. The postoperative course was uneventful. Histological findings were consistent with ulcerous acalculous cholecystitis. The patient was disease-free after a 3-month follow-up.
SPCBD is an uncommon condition in adults, and it is rarely reported in the literature. The pathogenesis of this disease is not clear and may be related to single or multiple factors. Usually, this disease is diagnosed in the postmortem. Early diagnosis and optimal surgical treatment are challenging.
This present case highlighted the preoperative diagnostic difficulties of the SPCBD. Emergent surgical management should be instituted in the shortest time possible to reduce the high mortality.
胆总管自发性穿孔(SPCBD)是一种罕见疾病,尤其在成年人中。一旦排除创伤和胆总管囊肿,病因通常为特发性。由于其表现常具有误导性,早期诊断往往困难。
作者报告了一名54岁男性病例,该患者为2型糖尿病已知病例,因急性腹痛持续2天前来我院急诊科就诊。
体格检查时,患者体温高达38.5°C,腹部膨隆且普遍紧张。腹部计算机断层扫描证实存在游离液体。此外,胆囊壁厚度增加,而胆囊扩张已缓解。由于探查未能显示腹水原因,作者进行了诊断性腹腔穿刺,抽出暗黄绿色腹水,提示胆汁渗漏。初步复苏后,进行了急诊剖腹探查术。作者发现SPCBD继发胆汁性腹膜炎。腹腔灌洗后,通过T管修复穿孔。术后病程顺利。组织学检查结果与溃疡性无结石胆囊炎一致。3个月随访后患者无疾病。
SPCBD在成年人中并不常见,文献中鲜有报道。该疾病的发病机制尚不清楚,可能与单一或多种因素有关。通常情况下,这种疾病在尸检时才被诊断出来。早期诊断和最佳手术治疗具有挑战性。
本病例突出了SPCBD术前诊断的困难。应尽快进行急诊手术治疗,以降低高死亡率。