Pediatric Gastroenterology and Hepatology Unit, Santobono-Pausilipon Children's Hospital, Via Mario Fiore, 6, Naples, Italy.
Maternal and Child Health Department, Sapienza - University of Rome, Polo Pontino, Latina, Italy.
Indian J Gastroenterol. 2024 Jun;43(3):567-577. doi: 10.1007/s12664-023-01472-3. Epub 2023 Nov 16.
Collagenous gastritis (CG) is a rare histopathological finding on gastric biopsies in children. It is associated with abdominal pain and iron deficiency anemia, usually not respondent to oral iron supplements. The aim of this study was to describe our experience in the management of pediatric patients with CG. Moreover, we propose to review the literature on this topic. We retrospectively reviewed all pediatric patients diagnosed with CG at our centre from January 2014 to January 2019. Three pediatric patients (2 F, mean age 12.3) were diagnosed with CG during the study period. Two presented with moderate and one with severe anemia. Symptoms were abdominal pain, asthenia and headache in two and asthenia and abdominal pain in one. All underwent upper and lower gastrointestinal endoscopy. All were firstly started with oral iron supplements with no benefit, principally due to poor compliance secondary to the worsening of the epigastric pain and proton pump inhibitor resistance. Therefore, they underwent ferric carboxymaltose (FCM) infusion with good clinical and laboratory response. Patients received a mean of two infusions/year, with stable hemoglobin levels and no adverse outcomes. Our review failed to identify a consistent response to specific treatments. Considering the apparent benign nature of the disease, symptomatic and supportive treatments are advisable. Iron deficiency anemia is largely present and therapy with oral iron supplements is not always successful. In our study, FCM infusion was effective in increasing the key blood indices in patients who poorly tolerated oral supplements.
胶原性胃炎(CG)是儿童胃活检中的一种罕见组织病理学发现。它与腹痛和缺铁性贫血有关,通常对口服铁补充剂没有反应。本研究旨在描述我们在管理 CG 儿科患者方面的经验。此外,我们还将对该主题的文献进行综述。我们回顾性分析了 2014 年 1 月至 2019 年 1 月期间在我们中心诊断为 CG 的所有儿科患者。研究期间有 3 名儿科患者(2 名女性,平均年龄 12.3 岁)被诊断为 CG。其中 2 例为中度贫血,1 例为重度贫血。症状为腹痛、乏力和头痛各 2 例,乏力和腹痛各 1 例。所有患者均行上消化道和下消化道内镜检查。所有患者最初均接受口服铁补充剂治疗,但无获益,主要是由于上腹痛加重和质子泵抑制剂耐药导致的依从性差。因此,他们接受了羧基麦芽糖铁(FCM)输注,临床和实验室反应良好。患者平均每年接受 2 次输注,血红蛋白水平稳定,无不良结局。我们的综述未能确定对特定治疗的一致反应。考虑到疾病的明显良性性质,建议采用对症和支持性治疗。缺铁性贫血很常见,口服铁补充剂治疗并不总是有效。在我们的研究中,FCM 输注可有效增加不耐受口服补充剂的患者的关键血液指标。