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一名12岁儿童胃内胰腺腺泡细胞化生:一例极其罕见的病例报告。

Pancreatic acinar cell metaplasia in the stomach of a 12-year-old child: An extremely rare case report.

作者信息

Issa Muhsen, Taleb Wafaa, Ibrahim Ali, Issa Rana

机构信息

Faculty of Medicine, Al-Andalus University for Medical Sciences, Tartus, Syria.

Cancer Research Center, Tishreen University, Lattakia, Syria.

出版信息

Medicine (Baltimore). 2025 Jul 25;104(30):e43591. doi: 10.1097/MD.0000000000043591.

Abstract

RATIONALE

Pancreatic acinar cell metaplasia of the gastric mucosa is characterized by the presence of clusters of pancreatic-like cells in the stomach. Although there are many instances of this condition in adults described in the medical literature, symptomatic cases in children are exceedingly rare.

PATIENT CONCERNS

A 12-year-old female patient presented to the pediatric clinic at Tishreen University Hospital complaining of postprandial nausea and recurrent periumbilical pain. The patient's symptoms were not accompanied by fever, diarrhea, or constipation. The patient's medical history was unremarkable. No abnormalities were noted on the physical examination.

DIAGNOSES

Biopsies taken during esophagogastroduodenoscopy revealed Helicobacter pylori-positive chronic gastritis.

INTERVENTIONS

The patient was started on omeprazole, clarithromycin, and metronidazole triple therapy, but with minimal improvement. Six months later, esophagogastroduodenoscopy was repeated because her symptoms persisted, and antral biopsies showed clusters of pancreatic-like cells with no signs of H. pylori.

OUTCOMES

The patient was diagnosed with pancreatic acinar cell metaplasia and put on symptomatic treatment, to no avail. One year after the initial diagnosis, esophagogastroduodenoscopy was redone, showing similar findings.

LESSONS

This report shows the development of pancreatic acinar cell metaplasia in a child after treatment for H. pylori. The clinical significance of pancreatic acinar cell metaplasia is not yet known because of the small number of cases documented in the literature, particularly among children.

摘要

原理

胃黏膜胰腺腺泡细胞化生的特征是胃内出现胰腺样细胞簇。尽管医学文献中有许多成人患此病的病例描述,但儿童出现症状的病例极为罕见。

患者情况

一名12岁女性患者到提什reen大学医院儿科门诊就诊,主诉餐后恶心和反复脐周疼痛。患者症状未伴有发热、腹泻或便秘。患者既往病史无异常。体格检查未发现异常。

诊断

食管胃十二指肠镜检查期间采集的活检显示幽门螺杆菌阳性慢性胃炎。

干预措施

患者开始接受奥美拉唑、克拉霉素和甲硝唑三联疗法,但改善甚微。六个月后,由于症状持续,再次进行食管胃十二指肠镜检查,胃窦活检显示有胰腺样细胞簇,无幽门螺杆菌迹象。

结果

患者被诊断为胰腺腺泡细胞化生并接受对症治疗,但无效。初始诊断一年后,再次进行食管胃十二指肠镜检查,结果相似。

经验教训

本报告显示了一名儿童在接受幽门螺杆菌治疗后发生胰腺腺泡细胞化生。由于文献中记录的病例数量较少,特别是在儿童中,胰腺腺泡细胞化生的临床意义尚不清楚。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dd/12303496/2c73e95e3989/medi-104-e43591-g001.jpg

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