First Case Report of Pancreatitis in Lyme disease

A. Baisse, S. Parreau, A. Abdeh, N. Pichon
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Abstract

A 49-year-old man, non-alcoholic forest worker, with no past medical history, consulted to the Emergency Department for fever and persistent abdominal pain for a week. The biological results including, C reactive protein (CRP), lipase, hepatic assessment were normal as well as contrast-enhanced abdominal Computed Tomography (CT). On the day after, the evolution was favorable under symptomatic treatment including nefopam and paracetamol and the patient was discharged from the hospital. One week later, the patient was admitted to the Emergency Department with an identical symptomatology. A posterior quadricipital peeling skin lesion, appeared two weeks earlier according to the patient, was observed (Figure 1a.) A gastroscopy, a colonoscopy, other abdominal CT and biological tests were performed. An inflammation biomarker elevation was observed (CRP: 180 mg/L and hyperleukocytosis: 13.3 G/L) without other biological abnormalities (lipase: 48 UI/L, ALAT: 48 UI/L). The endoscopic examinations and abdominal CT were normal. The patient was discharged from the hospital without any treatment. Half a month later, the patient was admitted to the Emergency Department for the third time and recurrence of the abdominal pain. The clinical examination found a hemodynamic stability, an abdominal pain of the left hypochondrium associated with a cutaneous ulcerative and non-progressive skin lesion in the same region as previously mentioned (Figure 1b.). The biological assessment found a very mild inflammatory syndrome (CRP 86 mg/L, Procalcitonin < 0.2 ng/mL, leukocytes 9.5 G/L), a high lipase level at 1714 IU/L without hepatocellular abnormalities. The third abdominal CT revealed an aspect of pancreatic necrosis with a pseudocyst (6 cm) at the tail of the pancreas, in contact with the splenic hile and the posterior wall of the stomach (Figure 1c.). The patient was hospitalized in Intensive Care Department with the diagnosis of pancreatitis.
莱姆病并发胰腺炎1例报告
49岁男性,非酒精性森林工人,无既往病史,因发烧和持续腹痛就诊于急诊科一周。生物学结果包括C反应蛋白(CRP),脂肪酶,肝脏评估正常,腹部计算机断层扫描(CT)增强。次日,经耐福泮、扑热息痛等对症治疗,病情发展良好,出院。一周后,患者以相同的症状被送入急诊科。观察到两周前出现的头侧后侧脱皮病变(图1a)。进行了胃镜检查、结肠镜检查、其他腹部CT检查和生物学检查。炎症标志物升高(CRP: 180 mg/L,白细胞增多症:13.3 G/L),无其他生物学异常(脂肪酶:48 UI/L, ALAT: 48 UI/L)。内窥镜检查及腹部CT检查均正常。病人未经任何治疗就出院了。半个月后,患者第三次住进急诊科,腹痛复发。临床检查发现血流动力学稳定,左侧胁肋腹痛,与先前提到的同一区域皮肤溃疡和非进行性皮肤病变相关(图1b)。生物学评估发现非常轻微的炎症综合征(CRP 86 mg/L,降钙素原< 0.2 ng/mL,白细胞9.5 G/L),脂肪酶高水平1714 IU/L,无肝细胞异常。第三次腹部CT显示胰腺坏死的侧面,胰腺尾部有一个假性囊肿(6厘米),与脾脏和胃后壁接触(图1c)。患者因诊断为胰腺炎而住进重症监护室。
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