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病例报告:罕见的良性胆道阻塞性疾病——嗜酸性胆管炎一例罕见病例。

Case report: Rare benign obstructive disease of the biliary tract-a rare case of eosinophilic cholangitis.

作者信息

Huang Xiao-Ning, Fang Qi-Min, Zhong Yu-Feng, Liu Jing

机构信息

Department of Radiology, The Second Affiliated Hospital, Nanchang University, Nanchang, Jiangxi, China.

Department of Pathology, Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.

出版信息

Front Med (Lausanne). 2024 Jan 17;10:1340667. doi: 10.3389/fmed.2023.1340667. eCollection 2023.

Abstract

OBJECTIVE

Eosinophilic cholangitis (EC) is an uncommon form of benign biliary obstruction. It frequently eludes accurate clinical diagnosis, leading to inappropriate treatment methods. It is our aspiration that this clinical report will impart comprehensive insights into EC and, specifically, the critical role of tomographic examination.

CASE SUMMARY

A 34-year-old man was urgently admitted to the hospital due to excruciating abdominal distress persisting for several hours. Following a six-day course of anti-inflammatory therapy, his symptoms displayed marginal improvement, prompting his discharge. He returned to the hospital a month later for re-examination on doctor's orders. Based on the results of the re-examination, the patient refused steroid hormone shock therapy and subsequently underwent laparoscopic left-lateral hepatic lobectomy in order to confirm the diagnosis. The preoperative absolute counts of eosinophils in the peripheral blood were documented as 2.3 × 10/L, 3.06 × 10/L, and 1.50 × 10/L consecutively; concurrently, the corresponding percentages of eosinophils were quantified at levels of 21.90%, 30.70%, and 19.20%. The subsequent postoperative pathological assessment unveiled EC as the definitive diagnosis. The patient has since remained free from disease recurrence and is presently alive.

CONCLUSION

When encountering a patient presenting with persistent elevation in absolute eosinophil count in peripheral blood, coupled with imaging manifestations suggestive of intrahepatic periductal inflammation, diagnosis of EC should be highly suspected. The most optimal diagnostic and therapeutic workflow for EC could entail CT-guided liver lesion biopsy, ensued by glucocorticoid pulse therapy, and finally, short-term monitoring utilizing CT or MRI (including T1WI, T2WI, DWI, CEMRI) techniques.

摘要

目的

嗜酸性胆管炎(EC)是一种罕见的良性胆道梗阻形式。它常常难以得到准确的临床诊断,导致治疗方法不当。我们希望这份临床报告能全面深入地介绍EC,特别是断层扫描检查的关键作用。

病例摘要

一名34岁男性因持续数小时的剧烈腹痛紧急入院。经过为期六天的抗炎治疗,他的症状仅有轻微改善,随后出院。一个月后,他遵医嘱返回医院进行复查。根据复查结果,患者拒绝接受类固醇激素冲击治疗,随后接受了腹腔镜左外侧肝叶切除术以明确诊断。术前外周血嗜酸性粒细胞绝对计数连续记录为2.3×10/L、3.06×10/L和1.50×10/L;同时,嗜酸性粒细胞的相应百分比分别量化为21.90%、30.70%和19.20%。随后的术后病理评估确诊为EC。此后,患者未出现疾病复发,目前仍然存活。

结论

当遇到外周血嗜酸性粒细胞绝对计数持续升高且伴有肝内胆管周围炎症影像学表现的患者时,应高度怀疑EC的诊断。EC最优化的诊断和治疗流程可能包括CT引导下肝病变活检,随后进行糖皮质激素脉冲治疗,最后利用CT或MRI(包括T1WI、T2WI、DWI、CEMRI)技术进行短期监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c384/10827930/a27f069fc375/fmed-10-1340667-g001.jpg

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