Management of collagenous gastritis in children: Case series and literature review

被引:0
作者
Isoldi, Sara [1 ,2 ,3 ]
Viola, Franca [4 ]
Cucchiara, Salvatore [4 ]
Dilillo, Anna [2 ]
Iorfida, Donatella [2 ]
Testi, Anna Maria [5 ]
Fiorentino, Francesco [6 ]
Mallardo, Saverio [2 ]
机构
[1] Santobono Pausilipon Childrens Hosp, Pediat Gastroenterol & Hepatol Unit, Via Mario Fiore 6, Naples, Italy
[2] Sapienza Univ Rome, Maternal & Child Hlth Dept, Latina, Italy
[3] Santa Maria Goretti Hosp, Latina, Italy
[4] Sapienza Univ Rome, Maternal & Child Hlth Dept, Pediat Gastroenterol & Liver Unit, Rome, Italy
[5] Sapienza Univ Rome, Dept Translat & Precis Med, Hematol, Rome, Italy
[6] Sapienza Univ Rome, Santa Maria Goretti Hosp, Pathol Unit, Latina, Italy
关键词
Collagenous gastritis; Ferric carboxymaltose; Iron deficiency anemia; Pediatric; Proton pump inhibitors; Treatment; IRON-DEFICIENCY ANEMIA; FERRIC CARBOXYMALTOSE; COLITIS; DISORDER;
D O I
10.1007/s12664-023-01472-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
引用
收藏
页码:567 / 577
页数:11
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