Acessibilidade / Reportar erro

Duodenal pathologies in children: a single-center experience Please cite this article as: Akbulut UE, Fidan S, Emeksiz HC, Ors OP. Duodenal pathologies in children: a single-center experience. J Pediatr (Rio J). 2018;94:273-8.

Abstract

Objective

Several studies have been performed concerning pathologies of the stomach and esophagus in the pediatric age group. However, there have been very few studies of duodenal pathologies in children. The authors aimed to examine the clinical, endoscopic, and histopathological characteristics, as well as the etiology of duodenal pathologies in children.

Method

Patients aged between 1 and 17 years undergoing esophagogastroduodenoscopy during two years at this unit, were investigated retrospectively. Demographic, clinical, endoscopic data, and the presence of duodenal pathologies, gastritis, and esophagitis were recorded in all of the children.

Results

Out of 747 children who underwent endoscopy, duodenal pathology was observed in 226 (30.3%) patients. Pathology was also present in the esophagus in 31.6% of patients and in the stomach in 58.4%. The level of chronic diarrhea was higher in patients with duodenal pathology when compared with those without duodenal pathology (p = 0.002, OR: 3.91, 95% CI: 1.59-9.57). Helicobacter pylori infection was more common in patients with pathology in the duodenum (59.3%).

Conclusion

Duodenal pathology was detected in 30.3% of the present patients. A significantly higher level of chronic diarrhea was observed in subjects with duodenal pathologies compared to those with no such pathology. The rate of Helicobacter pylori infection was considerably higher than that in previous studies. In addition, there is a weak correlation between endoscopic appearance and histology of duodenitis.

KEYWORDS
Duodenitis; Endoscopy; Children

Resumo

Objetivo

Foram feitos vários estudos com relação a patologias do estômago e esôfago na faixa etária pediátrica. Contudo, poucos estudos das patologias duodenais em crianças. Visamos a examinar as características clínicas, endoscópicas e histopatológicas, juntamente com a etiologia, das patologias duodenais em crianças.

Método

Foram investigados retrospectivamente pacientes entre 1 e 17 anos submetidos a esofagogastroduodenoscopia durante dois anos em nossa unidade. Os dados demográficos, clínicos e endoscópicos e a presença de patologias duodenais, gastrite e esofagite foram registrados com relação a todas as crianças.

Resultados

Das 747 crianças submetidas a endoscopia, 226 (30,3%) apresentaram patologia duodenal. A patologia também esteve presente no esôfago de 31,6% dos pacientes e no estômago de 58,4%. O nível de diarreia crônica foi maior nos pacientes com patologia duodenal, em comparação com os pacientes sem patologia duodenal (p = 0,002, RC: 3,91, IC de 95%: 1,59-9,57). Infecção por Helicobacter pylori foi mais comum em pacientes com patologia no duodeno (59,3%).

Conclusão

Foi detectada patologia duodenal em 30,3% de nossos pacientes. Um nível significativamente maior de diarreia crônica foi observado em indivíduos com patologias duodenais, em comparação aos sem patologia. A infecção por Helicobacter pylori esteve presente consideravelmente maior do que em estudos anteriores. Além disso, há uma fraca correlação entre a imagem endoscópica e a histologia de duodenite.

PALAVRAS-CHAVE
Duodenite; Endoscopia; Crianças

Introduction

Esophagogastroduodenoscopy (EGD) is a reliable technique widely used in the diagnosis of diseases of the esophagus, stomach, and proximal duodenum. The advantages of this method are that the internal surface of the organ undergoing endoscopy can be observed directly, pathological sampling from lesions can be performed, and treatment can be administered when necessary. Since its introduction in pediatric patients in 1970, the use of endoscopic procedures has increased dramatically.11 Noble AJ, Drouin E, Tamblyn R. Design of predictive models for positive outcomes of upper and lower gastrointestinal endoscopies in children and adolescents. J Pediatr Gastroenterol Nutr. 2008;46:409-13. Franciosi et al.22 Franciosi JP, Fiorino K, Ruchelli E, Shults J, Spergel J, Liacouras CA, et al. Changing indications for upper endoscopy in children during a 20-year period. J Pediatr Gastroenterol Nutr. 2010;51:443-7. reported that the number of upper endoscopic procedures increased by 12-fold between 1985 and 2005. As a consequence of this trend, new disorders of the GI tract and new pathologies were described in children.

In parallel to the increased use of EGD among children, numerous studies evaluating the pathologies of the stomach and esophagus in children have been performed. 33 Pashankar DS, Bishop WP, Mitros FA. Chemical gastropathy: a distinct histopathologic entity in children. J Pediatr Gastroenterol Nutr. 2002;35:653-7.,44 Papadopoulou A, Koletzko S, Heuschkel R, Dias JA, Allen KJ, Murch SH, et al. Management guidelines of eosinophilic esophagitis in childhood. J Pediatr Gastroenterol Nutr. 2014;58:107-18. However, there have been very few studies investigating the association between duodenal endoscopic findings and histologic diagnosis in the pediatric population. Alper et al.55 Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6. reported that the prevalence of duodenitis in children undergoing endoscopy was 12.7%, and the correlation between endoscopic appearance and histology was considered to be poor. In another study, Alabd Alrazzak et al.66 Alabd Alrazzak B, Husien T, Preston DL, Elitsur Y. Upper endoscopy in children: do symptoms predict positive findings?. Clin Pediatr (Phila). 2014;53:474-8. observed an 11% rate of duodenitis prevalence, while in a study of 1000 children undergoing EGD, Sheiko et al.77 Sheiko MA, Feinstein JA, Capocelli KE, Kramer RE. Diagnostic yield of EGD in children: a retrospective single-center study of 1000 cases. Gastrointest Endosc. 2013;78:47-54. observed endoscopic disorder in the duodenum at a rate of 9.9% and histopathologic disorder at a rate of 10.7%.

The aim of the study was to assess the endoscopic and histopathologic features of duodenal disorders with respect to age groups in children undergoing diagnostic EGD for the first time.

Methods

The authors retrospectively reviewed all upper endoscopic charts of children between the ages of 1 and 17 years who underwent diagnostic EGD at Kanuni Training and Research Hospital Pediatric Gastroenterology Department, Turkey, between September 2014 and September 2016. Clinical data, demographic characteristics, and histopathology findings were also reviewed. Patients with known gastrointestinal disease (such as celiac disease, Crohn's disease, and ulcerative colitis), with neurodevelopmental delay (such as cerebral palsy), and those undergoing endoscopy for therapeutic purposes were excluded. In children undergoing endoscopy more than once, the data of the first EGD was recorded. This study was performed in agreement with the Declaration of Helsinki and following the approval of the Local Ethics Committee. Symptoms were grouped into growth retardation, chronic anemia, chronic diarrhea, chronic abdominal pain, dyspepsia, and reflux symptoms (vomiting, chest pain, regurgitation, and eructation).88 Vandenplas Y, Rudolph CD, Di Lorenzo C, Hassall E, Liptak G, Mazur L, et al. Pediatric gastroesophageal reflux clinical practice guidelines: joint recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN). J Pediatr Gastroenterol Nutr. 2009;49:498-547. Chronic abdominal pain was defined as three or more bouts in at least a three-month period.99 Apley J, Naish N. Recurrent abdominal pains: a field survey of 1000 school children. Arch Dis Child. 1958;33:165-70. Chronic diarrhea was defined as that lasting more than 14 days.1010 Guarino A, Lo Vecchio A, Berni Canani R. Chronic diarrhoea in children. Best Pract Res Clin Gastroenterol. 2012;26:649-61. The patients were stratified into four groups with respect to the growth stages; infants (0-2 years), preschoolers (3-5 years), school-aged children (6-11 years), and adolescents (>12 years).

All procedures were performed by the same experienced gastroenterologist (U.E.A.) on an video gastroscopy device (Olympus, GIF-H180, PA, USA). Mucosal breaks of >5 mm observed in endoscopy were defined as ulcers.1111 Egbaria R, Levine A, Tamir A, Shaoul R. Peptic ulcers and erosions are common in Israeli children undergoing upper endoscopy. Helicobacter. 2008;13:62-8. In addition, gross endoscopic findings such as scalloping, nodularity, loss of mucosal folds, or mosaic pattern in the duodenum were regarded as pathological findings. 1212 Olds G, McLoughlin R, O'Morian C, Sivak MV. Celiac disease for the endoscopist. Gastrointest Endosc. 2002;56:407-15.

13 Wildi SM, Glenn TF, Woolson RF, Wang W, Hawes RH, Wallace MB. Is esophagoscopy alone sufficient for patients with reflux symptoms?. Gastrointest Endosc. 2004;59:349-54.
-1414 Turner D, Griffiths AM. Esophageal, gastric, and duodenal manifestations of IBD and the role of upper endoscopy in IBD diagnosis. Curr Gastroenterol Rep. 2007;9:475-8. Non-specific findings such as hyperemia, increased or decreased vascularity, and pallor were not regarded as pathological.1515 Thakkar K, Chen L, Tessier ME, Gilger MA. Outcomes of children after esophagogastroduodenoscopy for chronic abdominal pain. Clin Gastroenterol Hepatol. 2014;12:963-9.

At least two biopsies were taken from all patients from the esophagus, stomach (antrum), and the second part of the duodenum. All the initial examinations were performed by experienced gastrointestinal pathologists blinded to the patients' clinical status and endoscopic findings. For cases with a diagnosis of duodenum pathology, all microscopic sections were retrieved and reviewed by two experienced pathologists, and the diagnosis of duodenum pathology was confirmed in all patients. Increased intraepithelial lymphocytes in the duodenum (>30 lymphocytes) and chronic changes involving neutrophilic infiltration or villous/crypt structural changes were regarded as duodenitis.1616 Carmack SW, Genta RM. The diagnostic value of the duodenal biopsy: a clinico-pathologic analysis of 28,000 patients. Dig Liver Dis. 2010;42:485-9. Patients at >stage 2 according to the modified Marsh criteria and with positive serology were diagnosed with celiac disease.1717 Koletzko S, Niggemann B, Arato A, Dias JA, Heuschkel R, Husby S, et al. Diagnostic approach and management of cow's-milk protein allergy in infants and children: ESPGHAN GI Committee practical guidelines. J Pediatr Gastroenterol Nutr. 2012;55:221-9. The diagnosis of eosinophilic gastroenteritis (EG) was established upon observation of ≥25 eosinophils in one high-power field in the duodenum following the exclusion of parasitic infections, Helicobacter pylori infection, celiac disease, inflammatory bowel disease, hypereosinophilic syndrome, malignity, and connective tissue diseases (such as Churg-Strauss syndrome).1818 Henderson CJ, Ngeow J, Collins MH, Martin LJ, Putnam PE, Abonia JP, et al. Increased prevalence of eosinophilic disorders in pediatric PTEN hamartoma tumor syndromes. J Pediatr Gastroenterol Nutr. 2014;58:553-60. Endoscopic and/or histopathological abnormalities in the duodenum were considered as duodenal pathology. The antral biopsy specimens were fixed in 10% formalin and stained with hematoxylin and eosin (H&E). Giemsa staining was used to confirm the presence of H. pylori. Microscopic detection of gastric non-Helicobacter pylori helicobacter (NHPH), either in histologic sections or in smears, is the most widely used diagnostic method and usually allows differentiation between H. pylori and NHPH infections.1919 Baele M, Pasmans F, Flahou B, Chiers K, Ducatelle R, Haesebrouck F. Non-Helicobacter pylori helicobacters detected in the stomach of humans comprise several naturally occurring Helicobacter species in animals. FEMS Immunol Med Microbiol. 2009;55:306-13. For example, Helicobacter felis is characterized by the presence of periplasmic fibrils. Helicobacter salomonis is a less tightly coiled bacteria usually with a one periplasmic fibril, whereas long spiral shape is the morphological distinction of Helicobacter heilmannii.1919 Baele M, Pasmans F, Flahou B, Chiers K, Ducatelle R, Haesebrouck F. Non-Helicobacter pylori helicobacters detected in the stomach of humans comprise several naturally occurring Helicobacter species in animals. FEMS Immunol Med Microbiol. 2009;55:306-13. Findings such as papillary elongation in the esophagus, basal cell hyperplasia, and an increase in intraepithelial neutrophils were evaluated in favor of reflux esophagitis.2020 Zentilin P, Savarino V, Mastracci L, Spaggiari P, Dulbecco P, Ceppa P, et al. Reassessment of the diagnostic value of histology in patients with GERD, using multiple biopsy sites and an appropriate control group. Am J Gastroenterol. 2005;100:2299-306. Eosinophilia in the esophagus was defined as ≥30 eosinophils in one high-power field and/or observation of eosinophilic microabscesses.44 Papadopoulou A, Koletzko S, Heuschkel R, Dias JA, Allen KJ, Murch SH, et al. Management guidelines of eosinophilic esophagitis in childhood. J Pediatr Gastroenterol Nutr. 2014;58:107-18. In these cases, EGD was repeated subsequent to the administration of high-dose PPI (lansoprazole 1 mg/kg per dose, twice daily) for eight weeks. Persisting eosinophilia in the esophagus was regarded as eosinophilic esophagitis.44 Papadopoulou A, Koletzko S, Heuschkel R, Dias JA, Allen KJ, Murch SH, et al. Management guidelines of eosinophilic esophagitis in childhood. J Pediatr Gastroenterol Nutr. 2014;58:107-18. Reflux esophagitis and eosinophilic esophagitis were evaluated under the group of esophagitis. Gastritis is diagnosed by the presence of mixed inflammatory infiltrate.55 Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6.

Data were analyzed using SPSS software (SPSS for Windows, version 13.0, Chicago, USA). Descriptive data were expressed as mean ± standard deviation (SD), with the Student's t-test for independent paired samples was used to compare normally distributed variables between two groups, and the Mann-Whitney U test, for non-normally distributed variables. The chi-squared test was used to compare categoric variables. Statistical significance was set at p < 0.05.

Results

During the two-year study period, 870 EGDs were performed in total. A total of 123 EGDs were excluded, including repeated EGD procedures (n = 67), EGD of patients with previously known gastrointestinal disease (n = 18), retarded neuromotor development (n = 14), or undergoing procedures for therapeutic purposes (n = 24). Finally, 747 patients were enrolled in the study. The patients were aged between 1 and 17 years and the majority was female (n = 458, 61.3%). One patient (0.1%) was an infant, 41 (5.5%) were preschoolers, 242 (32.3%) were school-aged children, and 463 patients (62.1%) were adolescents. Duodenal pathology was observed in 226 (30.3%) patients. Pathology was also present in the esophagus in 31.6% of patients and in the stomach in 58.4%. Of the 236 esophageal pathologies, 232 were reflux esophagitis and four were eosinophilic esophagitis.

The mean age of the patients with pathology in the duodenum was 12.9 years (range 4-17 years) and the majority was female (58.4%). The demographic characteristics of patients with gastrointestinal symptoms and accompanying pathologies are shown in Table 1. The level of chronic diarrhea was higher in patients with duodenal pathology compared to those without duodenal pathology (p = 0.002, OR: 3.91, 95% CI: 1.59-9.57). It was observed that reflux symptoms were more common in preschoolers; dyspeptic complaints, in school-aged children; and chronic anemia, in adolescents (p < 0.05; Table 2). H. pylori gastritis and esophagitis were more common in patients with pathology in the duodenum compared to those without pathology (p < 0.001, OR: 3.43, 95% CI: 2.48-4.76 vs. p < 0.001, OR: 0.40, 95% CI: 0.29-0.56; Table 1).

Table 1
Demographic characteristics of patients with gastrointestinal symptoms and accompanying pathologies.
Table 2
Comparison of gastrointestinal symptoms according to age groups.

Endoscopy determined ulcer in the bulbus in 59 patients (7.8%), scalloping in eight (1.0%), and nodularity in eight (1.0%). The endoscopic and histopathological characteristics of the duodenum are shown in Table 3. Histopathological examination of the duodenum in patients with ulcer in the bulbus revealed nonspecific duodenitis in 96.6%. Normal histopathological findings were observed in one patient. Abdominal pain persisting for 6 months, weight loss and sedimentation elevation were present in a 16-year-old girl with ulcer in the bulbus, in whom granuloma was determined on histopathological examination; this patient was diagnosed with Crohn's disease. H. pylori gastritis was present in 51 (86.4%) of the patients with ulcer in the bulbus. Anti-tissue transglutaminase IgA positivity was present in all patients with scalloping in the duodenum, and these were diagnosed with celiac disease following histopathological examination. Among the patients with nodularity in the duodenum, eosinophilic enteropathy was diagnosed in two (22.2%), giardiasis in two (22.2%), and celiac disease in one (11.1%). Duodenal disorders were more common in the adolescent group when compared with the other groups (Table 2).

Table 3
Endoscopic and histopathological characteristics of the duodenum.

Pathology was identified with histopathological examination in 151 (22.4%) of the 672 patients in whom pathology in the duodenum was not determined with endoscopy. Nonspecific duodenitis was present in 141 patients (93.3%), giardiasis in seven (4.6%), eosinophilic enteritis in two (1.4%), and celiac disease in one (0.7%). Abnormality was identified histopathologically in 74 (98.6%) of the 75 patients in whom pathology was determined at endoscopy (Table 3).

Discussion

Diagnostic sensitivity for the diagnosis of GIS disorders has increased remarkably with the advances in imaging technology and the increase in the use of EGD. Previous studies have reported an incidence of duodenitis in children undergoing endoscopy of 10.7-12.7%. 55 Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6.,66 Alabd Alrazzak B, Husien T, Preston DL, Elitsur Y. Upper endoscopy in children: do symptoms predict positive findings?. Clin Pediatr (Phila). 2014;53:474-8. Alabd Alrazzak et al.66 Alabd Alrazzak B, Husien T, Preston DL, Elitsur Y. Upper endoscopy in children: do symptoms predict positive findings?. Clin Pediatr (Phila). 2014;53:474-8. observed a prevalence of duodenitis of 11.0%, while in a study of 1000 children undergoing EGD, Sheiko et al.77 Sheiko MA, Feinstein JA, Capocelli KE, Kramer RE. Diagnostic yield of EGD in children: a retrospective single-center study of 1000 cases. Gastrointest Endosc. 2013;78:47-54. diagnosed duodenal pathology in 9.9% of their sample when using endoscopy and in 10.7% when using histopathological methods. Recently, Alper et al.55 Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6. investigated 2772 children undergoing EGD and diagnosed duodenitis in 12.7%. The incidence of overall duodenal disorders in the present cohort was 30.3%.

In agreement with Alper et al.,55 Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6. the most common indication for EGD in this study was Chronic abdominal pain (CAP). Those authors reported a higher level of CAP in subjects with duodenal pathology than in those without. In the current study, however, no difference was observed between subjects with or without duodenal pathology in terms of the prevalence of CAP. A significantly higher level of chronic diarrhea was observed in subjects with duodenal pathologies compared to those with no such pathology. The American Society for Gastrointestinal Endoscopy recommends EGD in cases of chronic diarrhea, particularly if absorption disorder is suspected.2121 Shen B, Khan K, Ikenberry SO, Anderson MA, Banerjee S, et al. The role of endoscopy in the management of patients with diarrhea. Gastrointest Endosc. 2010;71:887-92.

H. pylori infection was present in 59.3% of the current study patients with duodenal pathology. This level is considerably higher than that observed in previous studies. For example, while Alper et al.55 Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6. made specific diagnosis in 64% of patients with duodenitis (the majority consisting of celiac disease and inflammatory bowel disease, while H. pylori was observed at the low level of 6%), 36% of patients were diagnosed with nonspecific duodenitis. However, although the prevalence of H. pylori infection ranges from 6.5% to 31.0% in Europe, the reported prevalence is 53.0% to 66.3% in Turkey. 2222 Ceylan A, Kirimi E, Tuncer O, Turkdoğan K, Ariyuca S, Ceylan N. Prevalence of Helicobacter pylori in children and their family members in a district in Turkey. J Health Popul Nutr. 2007;25:422-7.,2323 Selimoglu MA, Ertekin V, Inandi T. Seroepidemiology of Helicobacter pylori infection in children living in eastern Turkey. Pediatr Int. 2002;44:666-9. In a study of 751 children undergoing EGD in Israel, a country with a high prevalence of H. pylori infection alike Turkey, Egbaria et al.1111 Egbaria R, Levine A, Tamir A, Shaoul R. Peptic ulcers and erosions are common in Israeli children undergoing upper endoscopy. Helicobacter. 2008;13:62-8. identified duodenal ulcer in 26 (3.5%) cases and H. pylori in 14 (∼54%) of these. A prospective study of 303 children in Saudi Arabia indicated the presence of H. pylori in 14 (56%) of 25 children with duodenal ulcer.2424 Hasosah M, Satti M, Shehzad A, Alsahafi A, Sukkar G, Alzaben A, et al. Prevalence and risk factors of Helicobacter pylori infection in Saudi children: a three-year prospective controlled study. Helicobacter. 2015;20:56-63. These results show that H. pylori infection bears a high level of responsibility for duodenal pathologies in communities in which this agent is widespread.

Several studies have shown that the prevalence of H. pylori infection increases with age. 2525 Cheng MT, Hwang KL, Tsao LY, Wang CH, Chaou WT, Chang YJ, et al. Using enzyme immunoassay to detect Helicobacter pylori stool antigen for investigating the prevalence of Helicobacter pylori infection in children and adolescents in Changhua. Acta Paediatr Taiwan. 2002;43:133-9.,2626 Rodrigues MN, Queiroz DM, Bezerra Filho JG, Pontes LK, Rodrigues RT, Braga LL. Prevalence of Helicobacter pylori infection in children from an urban community in North-East Brazil and risk factors for infection. Eur J Gastroenterol Hepatol. 2004;16:201-5. It has been observed at younger ages in developing countries, whereas the infection is more common in older ages in developed countries.2424 Hasosah M, Satti M, Shehzad A, Alsahafi A, Sukkar G, Alzaben A, et al. Prevalence and risk factors of Helicobacter pylori infection in Saudi children: a three-year prospective controlled study. Helicobacter. 2015;20:56-63. In a recent pediatric study from Turkey, Ozbey et al. reported that the prevalence of H. pylori infection among children reaches its peak between the ages of 13 and 18 years.2727 Ozbey G, Dogan Y, Demiroren K, Ozercan IH. Prevalence of Helicobacter pylori in children in eastern Turkey and molecular typing of isolates. Braz J Microbiol. 2015;46:505-11. Similar to that study, in the present study H. pylori infection was more common in the adolescent age group. Parallel to the increase in the incidence of H. pylori infection with age, duodenal pathologies were also observed at a higher rate in the adolescent age group.

In a multicenter study conducted in Europe, the incidence of duodenal ulcer in children undergoing EGD was reported as 2.4%.2828 Kalach N, Bontems P, Koletzko S, Mourad-Baars P, Shcherbakov P, Celinska-Cedro D, et al. Frequency and risk factors of gastric and duodenal ulcers or erosions in children: a prospective 1-month European multicenter study. Eur J Gastroenterol Hepatol. 2010;22:1174-81. In Israel, this rate was 3.5%.1111 Egbaria R, Levine A, Tamir A, Shaoul R. Peptic ulcers and erosions are common in Israeli children undergoing upper endoscopy. Helicobacter. 2008;13:62-8. In the present study, the incidence of ulcer in duodenum was 7.8%. The difference in the duodenal ulcer incidence between the studies may be due to the differences in the dietary habits and socio-cultural levels of the communities and use of gastro-protective drugs before endoscopy.

A weak correlation has been observed between endoscopic findings and histopathological results in previous studies. 55 Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6.,2929 Long FR, Kramer SS, Markowitz RI, Liacouras CA. Duodenitis in children: correlation of radiologic findings with endoscopic and pathologic findings. Radiology. 1998;206:103-8.,3030 Kori M, Gladish V, Ziv-Sokolovskaya N, Huszar M, Beer-Gabel M, Reifen R. The significance of routine duodenal biopsies in pediatric patients undergoing upper intestinal endoscopy. J Clin Gastroenterol. 2003;37:39-41. In a study of 75 children, Long et al.2929 Long FR, Kramer SS, Markowitz RI, Liacouras CA. Duodenitis in children: correlation of radiologic findings with endoscopic and pathologic findings. Radiology. 1998;206:103-8. reported that endoscopic appearance was 54% sensitive in estimating duodenitis. In a study by Alper et al.,55 Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6. in which a biopsy was performed in all patients, as in the present research, sensitivity was determined at 37%. Studies advocating the performance of routine duodenal biopsies in pediatric populations are lacking, and the practice among pediatric gastroenterologists is diverse. Kori et al.3030 Kori M, Gladish V, Ziv-Sokolovskaya N, Huszar M, Beer-Gabel M, Reifen R. The significance of routine duodenal biopsies in pediatric patients undergoing upper intestinal endoscopy. J Clin Gastroenterol. 2003;37:39-41. observed histopathological abnormalities in 35 (17.4%) of 201 patients with a normal endoscopic duodenal appearance. Several studies reported that the diagnosis of celiac disease was made and even granulomas, cryptitis and villus structure disorders were detected by histopathological evaluation of duodenal biopsies of some patients with normal duodenum appearance at endoscopy. 55 Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6.,3030 Kori M, Gladish V, Ziv-Sokolovskaya N, Huszar M, Beer-Gabel M, Reifen R. The significance of routine duodenal biopsies in pediatric patients undergoing upper intestinal endoscopy. J Clin Gastroenterol. 2003;37:39-41. Despite the high consensus of pathologists to identify histologic anomalies, there is considerable variability in the identification and classification of endoscopic abnormalities among endoscopists.77 Sheiko MA, Feinstein JA, Capocelli KE, Kramer RE. Diagnostic yield of EGD in children: a retrospective single-center study of 1000 cases. Gastrointest Endosc. 2013;78:47-54. In the current study, histopathological abnormality was also observed in a significant proportion (22.4%) of patients with a normal endoscopic duodenal appearance. The present findings suggest that a routine biopsy should be performed during EGD regardless of endoscopic appearance and endoscopy indications in children. This may minimize the overlooking of certain GIS disorders that may be clinically significant and can be remedied by appropriate treatment. Moreover, by performing a routine biopsy, the risks related to unjustifiable treatment or those associated with sedation or intervention during a repeat endoscopy procedure could be eliminated; the cost increase would also be avoided.

The present study has some limitations. It was retrospective in design. The number of patients in the infant group was low, therefore the duodenal disorders in that age group could not be evaluated. In addition, it was carried out in a single center; therefore, it may not fully reflect the duodenal disorders in different populations.

In conclusion, a higher level of duodenal pathologies was observed in this study involving both endoscopic and histopathological examination of duodenal pathologies compared to previous studies, and a high level of H. pylori infection was determined to accompany such pathologies. This variation among studies may be due to the fact that they were performed in different societies and patient populations. Further studies involving different communities and larger patient numbers are therefore needed to determine the prevalence, etiology, and clinical characteristics of duodenal pathologies. Another finding of this study was that histopathological abnormalities were observed at a considerable rate even in patients with normal endoscopic appearance. It can be suggested that the inclusion of routine duodenal biopsies as part of upper endoscopy in pediatric patients to be considered favorably. This practice may yield additional pathologic findings that might otherwise have been missed and may have clinical significance. It should be performed regardless of the indication for endoscopy or the general appearance of the mucosa.

  • Please cite this article as: Akbulut UE, Fidan S, Emeksiz HC, Ors OP. Duodenal pathologies in children: a single-center experience. J Pediatr (Rio J). 2018;94:273-8.

References

  • 1
    Noble AJ, Drouin E, Tamblyn R. Design of predictive models for positive outcomes of upper and lower gastrointestinal endoscopies in children and adolescents. J Pediatr Gastroenterol Nutr. 2008;46:409-13.
  • 2
    Franciosi JP, Fiorino K, Ruchelli E, Shults J, Spergel J, Liacouras CA, et al. Changing indications for upper endoscopy in children during a 20-year period. J Pediatr Gastroenterol Nutr. 2010;51:443-7.
  • 3
    Pashankar DS, Bishop WP, Mitros FA. Chemical gastropathy: a distinct histopathologic entity in children. J Pediatr Gastroenterol Nutr. 2002;35:653-7.
  • 4
    Papadopoulou A, Koletzko S, Heuschkel R, Dias JA, Allen KJ, Murch SH, et al. Management guidelines of eosinophilic esophagitis in childhood. J Pediatr Gastroenterol Nutr. 2014;58:107-18.
  • 5
    Alper A, Hardee S, Rojas-Velasquez D, Escalera S, Morotti RA, Pashankar DS. Prevalence and clinical, endoscopic, and pathological features of duodenitis in children. J Pediatr Gastroenterol Nutr. 2016;62:314-6.
  • 6
    Alabd Alrazzak B, Husien T, Preston DL, Elitsur Y. Upper endoscopy in children: do symptoms predict positive findings?. Clin Pediatr (Phila). 2014;53:474-8.
  • 7
    Sheiko MA, Feinstein JA, Capocelli KE, Kramer RE. Diagnostic yield of EGD in children: a retrospective single-center study of 1000 cases. Gastrointest Endosc. 2013;78:47-54.
  • 8
    Vandenplas Y, Rudolph CD, Di Lorenzo C, Hassall E, Liptak G, Mazur L, et al. Pediatric gastroesophageal reflux clinical practice guidelines: joint recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN). J Pediatr Gastroenterol Nutr. 2009;49:498-547.
  • 9
    Apley J, Naish N. Recurrent abdominal pains: a field survey of 1000 school children. Arch Dis Child. 1958;33:165-70.
  • 10
    Guarino A, Lo Vecchio A, Berni Canani R. Chronic diarrhoea in children. Best Pract Res Clin Gastroenterol. 2012;26:649-61.
  • 11
    Egbaria R, Levine A, Tamir A, Shaoul R. Peptic ulcers and erosions are common in Israeli children undergoing upper endoscopy. Helicobacter. 2008;13:62-8.
  • 12
    Olds G, McLoughlin R, O'Morian C, Sivak MV. Celiac disease for the endoscopist. Gastrointest Endosc. 2002;56:407-15.
  • 13
    Wildi SM, Glenn TF, Woolson RF, Wang W, Hawes RH, Wallace MB. Is esophagoscopy alone sufficient for patients with reflux symptoms?. Gastrointest Endosc. 2004;59:349-54.
  • 14
    Turner D, Griffiths AM. Esophageal, gastric, and duodenal manifestations of IBD and the role of upper endoscopy in IBD diagnosis. Curr Gastroenterol Rep. 2007;9:475-8.
  • 15
    Thakkar K, Chen L, Tessier ME, Gilger MA. Outcomes of children after esophagogastroduodenoscopy for chronic abdominal pain. Clin Gastroenterol Hepatol. 2014;12:963-9.
  • 16
    Carmack SW, Genta RM. The diagnostic value of the duodenal biopsy: a clinico-pathologic analysis of 28,000 patients. Dig Liver Dis. 2010;42:485-9.
  • 17
    Koletzko S, Niggemann B, Arato A, Dias JA, Heuschkel R, Husby S, et al. Diagnostic approach and management of cow's-milk protein allergy in infants and children: ESPGHAN GI Committee practical guidelines. J Pediatr Gastroenterol Nutr. 2012;55:221-9.
  • 18
    Henderson CJ, Ngeow J, Collins MH, Martin LJ, Putnam PE, Abonia JP, et al. Increased prevalence of eosinophilic disorders in pediatric PTEN hamartoma tumor syndromes. J Pediatr Gastroenterol Nutr. 2014;58:553-60.
  • 19
    Baele M, Pasmans F, Flahou B, Chiers K, Ducatelle R, Haesebrouck F. Non-Helicobacter pylori helicobacters detected in the stomach of humans comprise several naturally occurring Helicobacter species in animals. FEMS Immunol Med Microbiol. 2009;55:306-13.
  • 20
    Zentilin P, Savarino V, Mastracci L, Spaggiari P, Dulbecco P, Ceppa P, et al. Reassessment of the diagnostic value of histology in patients with GERD, using multiple biopsy sites and an appropriate control group. Am J Gastroenterol. 2005;100:2299-306.
  • 21
    Shen B, Khan K, Ikenberry SO, Anderson MA, Banerjee S, et al. The role of endoscopy in the management of patients with diarrhea. Gastrointest Endosc. 2010;71:887-92.
  • 22
    Ceylan A, Kirimi E, Tuncer O, Turkdoğan K, Ariyuca S, Ceylan N. Prevalence of Helicobacter pylori in children and their family members in a district in Turkey. J Health Popul Nutr. 2007;25:422-7.
  • 23
    Selimoglu MA, Ertekin V, Inandi T. Seroepidemiology of Helicobacter pylori infection in children living in eastern Turkey. Pediatr Int. 2002;44:666-9.
  • 24
    Hasosah M, Satti M, Shehzad A, Alsahafi A, Sukkar G, Alzaben A, et al. Prevalence and risk factors of Helicobacter pylori infection in Saudi children: a three-year prospective controlled study. Helicobacter. 2015;20:56-63.
  • 25
    Cheng MT, Hwang KL, Tsao LY, Wang CH, Chaou WT, Chang YJ, et al. Using enzyme immunoassay to detect Helicobacter pylori stool antigen for investigating the prevalence of Helicobacter pylori infection in children and adolescents in Changhua. Acta Paediatr Taiwan. 2002;43:133-9.
  • 26
    Rodrigues MN, Queiroz DM, Bezerra Filho JG, Pontes LK, Rodrigues RT, Braga LL. Prevalence of Helicobacter pylori infection in children from an urban community in North-East Brazil and risk factors for infection. Eur J Gastroenterol Hepatol. 2004;16:201-5.
  • 27
    Ozbey G, Dogan Y, Demiroren K, Ozercan IH. Prevalence of Helicobacter pylori in children in eastern Turkey and molecular typing of isolates. Braz J Microbiol. 2015;46:505-11.
  • 28
    Kalach N, Bontems P, Koletzko S, Mourad-Baars P, Shcherbakov P, Celinska-Cedro D, et al. Frequency and risk factors of gastric and duodenal ulcers or erosions in children: a prospective 1-month European multicenter study. Eur J Gastroenterol Hepatol. 2010;22:1174-81.
  • 29
    Long FR, Kramer SS, Markowitz RI, Liacouras CA. Duodenitis in children: correlation of radiologic findings with endoscopic and pathologic findings. Radiology. 1998;206:103-8.
  • 30
    Kori M, Gladish V, Ziv-Sokolovskaya N, Huszar M, Beer-Gabel M, Reifen R. The significance of routine duodenal biopsies in pediatric patients undergoing upper intestinal endoscopy. J Clin Gastroenterol. 2003;37:39-41.

Publication Dates

  • Publication in this collection
    May-Jun 2018

History

  • Received
    6 Feb 2017
  • Accepted
    17 Apr 2017
Sociedade Brasileira de Pediatria Av. Carlos Gomes, 328 cj. 304, 90480-000 Porto Alegre RS Brazil, Tel.: +55 51 3328-9520 - Porto Alegre - RS - Brazil
E-mail: jped@jped.com.br