Heterotopia of the gastric mucosa in the rectum: a clinical case report

Q4 Medicine
N. S. Kosmynina, M. Luchak
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引用次数: 0

Abstract

Heterotopic gastric mucosa is rare in the paediatric population, but it can pose a diagnostic challenge. This pathology can occur in any part of the digestive tract, from the oropharynx to the anorectal area. Most cases are observed in the esophagus, duodenum and hepatobiliary system, but the presence of this tissue in the rectum is extremely rare. Purpose - conduct a clinical description of a rare pathology in children in order to pay the doctors` attention to the need for comprehensive diagnosis of patients with hematochezia. Clinical case. We present a clinical case of a child with heterotopia of the gastric mucosa into the rectum. Symptoms included hematochezia and anal pain during the act of defecation, general weakness, and decreased appetite. These manifestations were observed for two years with periods of exacerbations and remissions on the background of conservative treatment. The final diagnosis was made on the basis of a biopsy of nodular formations of the rectum, detected by colonoscopy. Conclusions. Given the negative impact of the disease manifestations on the patient's quality of life and the potential risk of malignant transformation, the possibility of heterotopic gastric mucosa in the rectum with indeterminate bleeding from the lower gastrointestinal tract should be considered and a complete examination, including biopsy, should be performed. Once the diagnosis is confirmed, radical surgical removal is recommended. Initial conservative treatment with proton pump inhibitors provides only short-term relief and is accompanied by periods of exacerbation and remission. The final treatment is always surgical or endoscopic excision of the heterotopic mucosa. The research was carried out in accordance with the principles of the Helsinki Declaration. The informed consent of the patient was obtained for conducting the studies. No conflict of interests was declared by the authors.
直肠胃黏膜异位1例临床报告
异位胃黏膜在儿科人群中是罕见的,但它可以构成诊断的挑战。这种病理可以发生在消化道的任何部位,从口咽部到肛肠区。大多数病例见于食道、十二指肠和肝胆系统,但在直肠中出现这种组织极为罕见。目的:对儿童一种罕见的病理进行临床描述,以引起医生对便血患者需要进行综合诊断的重视。临床病例。我们报告一个儿童胃粘膜异位进入直肠的临床病例。症状包括排便时便溺和肛门疼痛,全身虚弱和食欲下降。这些表现在保守治疗的背景下观察了两年的恶化和缓解期。最终的诊断是在结肠镜检查直肠结节形成活检的基础上做出的。结论。考虑到疾病表现对患者生活质量的负面影响和潜在的恶性转化风险,应考虑直肠胃黏膜异位并下胃肠道不明出血的可能性,并进行包括活检在内的全面检查。一旦确诊,建议进行根治性手术切除。质子泵抑制剂的初始保守治疗只能提供短期缓解,并伴有加重和缓解期。最后的治疗通常是手术或内镜切除异位黏膜。这项研究是按照《赫尔辛基宣言》的原则进行的。获得患者的知情同意进行研究。作者未声明存在利益冲突。
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来源期刊
Suchasna pediatriia Ukrayina
Suchasna pediatriia Ukrayina Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
50
审稿时长
8 weeks
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