Ali Alsuheel Asseri, Ayed A Shati, Ibrahim Al-Benhassan, Shahad H Jabali, Taghreed A Alolah, Nada H Albarqi, Mansour S Alqahtani
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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. 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引用次数: 0
摘要
食管贲门失弛缓症(EA)是一种罕见的原发性食管运动障碍,被认为是婴幼儿吞咽困难的罕见病因。所提出的主要病理生理学原理与食管远端括约肌,尤其是奥尔巴赫肌层神经节细胞的缺失有关,进而导致食管运动障碍和下食管括约肌松弛功能失效。吞咽困难、呕吐、体重增加缓慢、咳嗽和反复吸入性肺炎是最常见的主诉症状。在此,我们报告了 3 例伴有慢性咳嗽和反复吸入性肺炎的 EA 患者。本研究回顾了 3 例具有 EA 典型症状的儿科患者。所有患者均因反复肺炎和疑似吸入综合征入院并转诊至儿科肺病科进行评估。所有患者均接受了食管钡餐造影检查,作为反复呕吐、吞咽困难和吸入性肺炎的气道检查的一部分。此外,所有患者还接受了其他相关先天性畸形的检查,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,并出现反复肺炎。所有患者都有孤立的EA,没有人有任何Allgrove综合征的证据。在进行上消化道内窥镜检查的同时,所有患者都接受了气囊扩张术。后来,所有患者都接受了腹腔镜海勒肌切开术,术后没有出现并发症,症状也得到了缓解。EA 在儿童中很罕见,但如果不及时治疗,可能会造成严重后果并危及生命。我们的病例强调了在儿童出现食道吞咽困难和反复肺炎时考虑贲门失弛缓症的重要性。已有多例小儿病例报道,呼吸系统受累是贲门失弛缓症的主要表现。这些病例强调了在对反复肺炎患儿进行鉴别诊断时考虑胃肠道疾病(尤其是 EA)的重要性。腹腔镜海勒肌切开术的早期诊断和治疗可为贲门失弛缓症患儿带来良好的治疗效果。
Esophageal achalasia presenting as recurrent pneumonia in children: A case series.
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.
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