Suppr超能文献

儿童食管失弛缓症表现为复发性肺炎:病例系列研究。

Esophageal achalasia presenting as recurrent pneumonia in children: A case series.

机构信息

Department of Child Health, College of Medicine, King Khalid University, Abha, Saudi Arabia.

Department of Pediatric Intensive Care Unit, Abha Maternity and Children's Hospital, Abha, Saudi Arabia.

出版信息

Medicine (Baltimore). 2024 Nov 1;103(44):e40402. doi: 10.1097/MD.0000000000040402.

Abstract

Esophageal achalasia (EA) is a rare primary esophageal motility disorder that is considered a rare etiology of dysphagia among infants and children. The proposed primary pathophysiology is related to the loss of ganglion cells in the distal esophageal sphincters, particularly in the Auerbachian muscle layer, which then leads to the dysmotility and failure of lower esophageal sphincter relaxation. Dysphagia, vomiting, poor weight gain, cough, and recurrent aspiration pneumonia are the most common presenting complaints. Herein, we report 3 cases of EA who presented with chronic cough and recurrent aspiration pneumonia. This study reviewed 3 pediatric patients with typical symptoms of EA. All the patients were admitted and referred to the pediatric pulmonology service for evaluation of recurrent pneumonia and suspected aspiration syndrome. All patients underwent a barium esophagogram as a part of the aerodigestive workup of recurrent vomiting, dysphagia, and aspiration pneumonia. Additionally, all the patients underwent workup for other associated congenital anomalies, which included echocardiography, brain magnetic resonance imaging, and an abdominal ultrasound. All patients had EA and presented with recurrent pneumonia. All patients had isolated EA, and none had any evidence of Allgrove syndrome. Pneumatic balloon dilatation was performed for all patients at the same time as the upper gastrointestinal endoscopy. Later, all the patients underwent a laparoscopic Heller myotomy and had no postoperative complications, and their symptoms resolved. EA is a rare condition in children, yet it can be a serious and life-threatening condition if left untreated. Our cases emphasize the significance of considering achalasia in children who experience esophageal dysphagia and recurrent pneumonia. Several pediatric cases have been reported in which respiratory involvement was the primary manifestation of achalasia. These cases highlight the importance of considering gastrointestinal disorders, particularly EA, in the differential diagnosis of children who experience recurrent pneumonia. Early diagnosis and treatment with laparoscopic Heller myotomy can lead to good outcomes for children with achalasia.

摘要

食管失弛缓症(EA)是一种罕见的原发性食管运动障碍,被认为是婴儿和儿童吞咽困难的罕见病因。提出的主要病理生理学与远端食管括约肌神经节细胞的丧失有关,特别是在奥伯巴赫肌层,这导致下食管括约肌动力障碍和松弛失败。吞咽困难、呕吐、体重增长不良、咳嗽和反复吸入性肺炎是最常见的表现。在此,我们报告了 3 例以慢性咳嗽和反复吸入性肺炎为表现的 EA 病例。本研究回顾了 3 例具有典型 EA 症状的儿科患者。所有患者均因反复肺炎和疑似吸入综合征而入院并转至儿科肺病科进行评估。所有患者均进行了钡餐食管造影检查,作为反复呕吐、吞咽困难和吸入性肺炎的气道消化道检查的一部分。此外,所有患者均进行了其他相关先天性异常的检查,包括超声心动图、脑磁共振成像和腹部超声检查。所有患者均患有 EA,并表现为反复肺炎。所有患者均为孤立性 EA,均无 Allgrove 综合征证据。在进行上消化道内镜检查的同时,对所有患者进行了气囊扩张。之后,所有患者均接受了腹腔镜 Heller 肌切开术,且无术后并发症,症状得到缓解。EA 在儿童中较为罕见,但如果不治疗,可能会导致严重的危及生命的情况。我们的病例强调了在出现食管吞咽困难和反复肺炎的儿童中考虑失弛缓症的重要性。已有几例儿科病例报告称,呼吸受累是失弛缓症的主要表现。这些病例强调了在反复肺炎的儿童中,考虑胃肠道疾病,特别是 EA,进行鉴别诊断的重要性。早期诊断和腹腔镜 Heller 肌切开术治疗可使 EA 患儿获得良好的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a87/11537638/13f823dcb4cc/medi-103-e40402-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验