Drnovšek Jan, Zidar Nina, Jeruc Jera, Šmid Lojze M, Vidmar Gaj, Štabuc Borut, Homan Matjaž
Department of Gastroenterology, University Medical Centre Ljubljana, Japljeva ulica 2, 1000 Ljubljana, Slovenia.
Faculty of Medicine, University of Ljubljana, Vrazov trg 2, 1000 Ljubljana, Slovenia.
Cancers (Basel). 2025 Jan 3;17(1):128. doi: 10.3390/cancers17010128.
BACKGROUND/OBJECTIVES: Gastric intestinal metaplasia (GIM) is considered an irreversible preneoplastic precursor for gastric adenocarcinoma in adults. However, its significance in children and the long-term outcome remain poorly understood.
All children diagnosed with GIM between 2000 and 2020 were identified at a large tertiary referral centre. Upon reaching adulthood (≥18 years), the patients were invited to undergo follow-up esophagogastroduodenoscopy (using narrow-band imaging additionally to high-definition white light endoscopy), with gastric biopsies obtained according to the updated Sydney protocol. Childhood and adulthood gastric biopsies were re-evaluated by two experienced gastrointestinal pathologists using Kreyberg staining.
Paediatric GIM was diagnosed in 178/14,409 (1.2%) esophagogastroduodenoscopies performed during the study period. Fifty adult patients with childhood GIM agreed to participate in the study. The mean age at childhood and adulthood endoscopies were 14.3 years (median 15) and 25.2 years (median 24), respectively. The mean follow-up interval was 10.5 years. All childhood GIM cases were classified as complete-type. Notably, GIM completely resolved in 41/50 of patients (82%) by the time of adulthood follow-up. No dysplasia or carcinoma was detected in any patient. Childhood infection, similar to other evaluated host-related factors, was not significantly associated with the persistence of GIM into adulthood (11.2% vs. 29.3%, = 0.41).
Childhood GIM was a rare finding but demonstrated a high rate of reversibility by adulthood regardless of status, with no cases of dysplasia or carcinoma observed during long-term follow-up.
背景/目的:胃肠化生(GIM)被认为是成人胃腺癌不可逆的癌前病变。然而,其在儿童中的意义及长期预后仍知之甚少。
在一家大型三级转诊中心识别出2000年至2020年间所有诊断为GIM的儿童。成年后(≥18岁),邀请患者接受随访食管胃十二指肠镜检查(除高清白光内镜检查外还使用窄带成像),并根据更新后的悉尼方案获取胃活检组织。两名经验丰富的胃肠病理学家使用Kreyberg染色对儿童期和成年期的胃活检组织进行重新评估。
在研究期间进行的14409例食管胃十二指肠镜检查中,诊断出178例(1.2%)儿童GIM。50例有儿童期GIM的成年患者同意参与研究。儿童期和成年期内镜检查的平均年龄分别为14.3岁(中位数15岁)和25.2岁(中位数24岁)。平均随访间隔为10.5年。所有儿童期GIM病例均分类为完全型。值得注意的是,到成年期随访时,41/50(82%)的患者GIM完全消退。所有患者均未检测到发育异常或癌症。儿童期感染与其他评估的宿主相关因素一样,与GIM持续至成年期无显著相关性(11.2%对29.3%,P = 0.41)。
儿童GIM是一种罕见发现,但成年后显示出高可逆率,无论感染状态如何,长期随访期间均未观察到发育异常或癌症病例。