PREVALENCE OF ESINOPHILIC ESOPHAGITIS AMONG ATOPIC EGYPTIAN POPULATION

Document Type : Original Article

Authors

1 Departments Internal Medicine, Faculty of Medicine, Al-Azhar University, Egypt

2 Departments Pathology*, Faculty of Medicine, Al-Azhar University, Egypt

Abstract

Background: Esinophilic esophagitis (EoE) is an atopic inflammatory disease of the esophagus that has become increasingly recognized in children and adults during the last decade. EoE is an atopic inflammatory disease of the esophagus that has become increasingly. Esinophils are typically present throughout the gastrointestinal tract since it is continuously exposed to foods, environmental allergens, toxins, and pathogens.
Objective: To evaluate the prevalence of esinophilic esophagitis in atopic patients.
Patients and Methods: This was a retrospective single center non randomized, observational study, 120 patients with age ranged from 18-60 years were recruited for this study. They were evaluated for esophageal symptoms using the frequency scale for the symptoms of gastro-esophageal reflux disease (GERD). It was conducted at Dermatology, Ear, Nose, and Throat (ENT), Ophthalmology and allergy clinic of Internal Medicine Departments, Al-Husein University Hospital. The study was done during the periods between July 2017 and September 2018.
Results: The mean total immunoglobulin E (IgE) of group II was higher than group I with significant statistical difference between both groups. As regards the mean blood esinophils of group II was higher than group I with significant statistical difference between both groups. Heartburn documented the higher presentations (83%), followed by regurgitation (58.5%), and a combination of other symptoms in patients. Only 6 cases out of 53 examined, endoscopic biopsies have histological features of EoE. The remaining 47 biopsies featured different histological diagnosis which included mild reflux esophagitis in 12 cases, moderate reflux esophagitis in 20 cases, and severe reflux esophagitis in 15 cases.
Conclusion: Atopic patients who suffered from esophagitis symptoms were assessed for EoE by endoscopic and histopathological examination especially if there was a high IgE level or increased blood esinophils.

Keywords


PREVALENCE OF ESINOPHILIC ESOPHAGITIS AMONG ATOPIC EGYPTIAN POPULATION

By

Ahmed Eid Sadek, Asem Mahmod Al-Sherif, Magdi El-Dahshan and Mohamed Samy Al-Hakim*

Departments Internal Medicine and Pathology*, Faculty of Medicine, Al-Azhar University, Egypt

Corresponding Author: Ahmed Eid Sadek, E-mail: dr.ahmed_sadek@gmail.com

ABSTRACT

Background: Esinophilic esophagitis (EoE) is an atopic inflammatory disease of the esophagus that has become increasingly recognized in children and adults during the last decade. EoE is an atopic inflammatory disease of the esophagus that has become increasingly. Esinophils are typically present throughout the gastrointestinal tract since it is continuously exposed to foods, environmental allergens, toxins, and pathogens.

Objective: To evaluate the prevalence of esinophilic esophagitis in atopic patients.

Patients and Methods: This was a retrospective single center non randomized, observational study, 120 patients with age ranged from 18-60 years were recruited for this study. They were evaluated for esophageal symptoms using the frequency scale for the symptoms of gastro-esophageal reflux disease (GERD). It was conducted at Dermatology, Ear, Nose, and Throat (ENT), Ophthalmology and allergy clinic of Internal Medicine Departments, Al-Husein University Hospital. The study was done during the periods between July 2017 and September 2018.

Results: The mean total immunoglobulin E (IgE) of group II was higher than group I with significant statistical difference between both groups. As regards the mean blood esinophils of group II was higher than group I with significant statistical difference between both groups. Heartburn documented the higher presentations (83%), followed by regurgitation (58.5%), and a combination of other symptoms in patients. Only 6 cases out of 53 examined, endoscopic biopsies have histological features of EoE. The remaining 47 biopsies featured different histological diagnosis which included mild reflux esophagitis in 12 cases, moderate reflux esophagitis in 20 cases, and severe reflux esophagitis in 15 cases.

Conclusion: Atopic patients who suffered from esophagitis symptoms were assessed for EoE by endoscopic and histopathological examination especially if there was a high IgE level or increased blood esinophils.

Keywords: Esinophilic, Atopic Egyptian, Esinophylic esophagitis.

 

 

INTRODUCTION

     Although the typical onset of esinophilic esophagitis (EoE) in childhood, the disease can be found in all age groups, and the symptoms tend to vary depending on the age of presentation. EOE is defined as clinic-pathologic disorder characterized by presence of> 15 esinophils per high power field (HPF) in one or more esophageal biopsy specimens (Furuta et al., 2011).

     The prevalence of the eosinophylic esophagitis is increasing among Caucasian, Asian and other ethnicities during the last years (Syed et al., 2012). Actually, it is not clear whether EOE is truly increasing or, if it is becoming more recognized by endoscopist and pathologists (Prasad et al., 2011). Some authors attribute this increase in prevalence rate of esinophilic esophagitis to parallel increases in atopic diseases, and they assume that there is an overlapping spectrum between GORD, allergy and esinophilic esophagitis (Sealock et al., 2010).

     Another referred this increase to parallel increasing in routine oesophageal biopsy rates (Syed et al., 2012). Until recently, there are no published reports in literature about the prevalence of eosinophylic esophagitis in Egyptian population.

     The aim of this study was to evaluate the prevalence of esinophilic esophagitis in atopic patients.

PATIENTS AND METHODS

     A retrospective single center non randomized, observational study, 120 patients with age ranged from 18-60 years were recruited for this study. They were evaluated for esophageal symptoms using the frequency scale for the symptoms of GERD. It was conducted at Dermatology, ENT, Ophthalmology and Allergy Clinic of Internal Medicine Department, Al-Husein University Hospital. The study was done during the periods between July 2017 and September 2018.

Inclusion criteria: Any patients with any type of atopy (Atopic rhinitis 20 patients, atopic eczema 20 patients, atopic conjunctivitis 20 patients, atopic asthma 60 patients) with history of dysphagia, food impaction and/or history suggestive GORD included in this study.

Exclusion criteria: Patients refusing to be enrolled in this study and patients with acute severe asthma.

The study was divided into two groups: Group (1) included atopic patients without esophageal symptoms (67), and Group (2) included atopic patients with esophageal symptoms (53). An informed written consent was signed by each patient after explaining the purpose and the methods of the study then approved by the local ethics committee.

     The selected atopic patients who had one or more of the esophageal symptoms such as reflux (heartburn or regurgitation) or symptoms of esophageal complications (dysphagia or history food impaction) (Cherian et al., 2010) underwent clinical assessment. They were subjected to upper GIT endoscopy under conscious sedition (by Midazolam 5–8 mg intravenously) after written consent for the sedation and the procedure for endoscopic assessment mainly for esophagus with biopsies (Ndraha, 2010). Endoscopic assessment of esophageal mucosa and cardia was done for presence of the GERD by presence of mucosal damage as the lower segment erosive esophagitis, esophageal ulcers, benign stenosis, and presence of sliding hiatal hernia with or without gastric contents refluxate. Endoscopic picture of the EoE such as esophageal circular rings (trachization), or whitish plague were also evaluated (Rosner and Milton, 2010). All patients were subjected to multiple esophageal mucosal biopsies (at least four esophageal mucosal biopsies were taken for each patient) for histopathological examination (Rawy and Mansour, 2015).

     This study involved 53 cases of esophageal biopsies. The specimens were received from two separate sites in the esophagus mainly proximal and middle with occasional lower esophageal part biopsy. From each paraffin-embedded block, two sections (3–4 μm each) were prepared for routine hematoxylin and eosin stain. All histological staining was performed in accordance with conventional procedures (Monjur, 2016). Sections stained by hematoxylin and eosin were examined to detect the number of esinophils in the esophageal mucosa, abscess formation, associated dysplasia, or reflux esophagitis; all cases having less than 15 eosinophils/HPF were excluded.

     The presence of intraepithelial esinophils, at least 15/ HPF in any one field, is considered diagnostic for EoE, while the presence of 6–14/HPF was considered indeterminate; esinophils may be diffuse or in clusters and may form micro-abscess. The esinophils should present only in the esophagus and the presence of esinophils in other parts of the intestine suggest esinophilic gastroenteritis (Asher and Dellon, 2014). Other less specific histological features that have occurred with EoE included intercellular edema, esinophilic degranulation, marked basal cell hyperplasia, and fibrosis of the lamina propria if the biopsy contained subepithelial layers. Histopathologic features without clinical correlation cannot diagnose EoE (Trevisani et al., 2010).

Statistical Analysis:

     Data were collected, revised, coded and entered to the Statistical Package for the Social Science (IBM SPSS) version 20. The qualitative data were presented as number and percentages while quantitative data were presented as mean, standard deviations and ranges. The comparison between two groups with qualitative data were done by using Chi-square test. The comparison between the two independent groups with quantitative data and parametric distribution were done by using independent t-test or Mann – Whitney U test.  The confidence interval was set to 95% and the margin of error accepted was set to 5%. P value < 0.05 was considered significant.

 

 

 

 

 

 

 

 

 

 

 

RESULTS

 

 

     This study included 120 patients diagnosed with atopy. The mean age was 52.80 ±10.78. The study included 52 men and 68 women. Patients were reviewed for GERD symptoms and 53 cases documented one or more positive GERD symptoms. Accordingly, the patients were divided into two groups: group I (67) included atopic patients without GERD symptoms and group II (53 asthmatic patients with GERD symptoms. The mean age of group II was higher than group I with no significant statistical differences between both groups. As regards sex results, it was found that females of group I was higher than group II with no significant statistical differences between both groups (Table 1).

 

 

Table (1):   Distribution of the studied cases according to demographic data and demographic results of both groups

Groups

Parameters

Group I

Group II

P-value

No.= 67

No.= 53

Sex

Female

39 (58.2%)

29 (54.7%)

0.701

Male

28 (41.8%)

24 (45.3%)

Age

Mean ± SD

52.44 ± 10.97

53.26 ± 10.61

0.679

Range

30 – 75

30 – 75

 

 

     The Median Total IgE of group II was higher than group I with highly significant statistical differences between both groups. The Median blood esinophils of group II was higher than group I with significant statistical differences between both groups (Table 2).

 

 

Table (2):   Comparison between the results of both groups regarding spirometer

Groups

Parameters

Group I

Group II

P-value

No.= 67

No.= 53

Total IgE

Mean ± SD

102.43 ± 105.10

147.15 ± 41.20

0.001

Range

24 – 898

84 – 190

Blood esinophils

Mean ± SD

10.39 ± 5.03

17.08 ± 5.52

0.001

Range

3 – 29

8 – 29

Group I: atopic patients without GERD symptoms.

Group II: atopic patients with GERD symptoms.

 

 

 

 

 

 

 

 

 

 

 

 

 

     The number and percentage of different symptoms and signs for all patients. Heartburn documented the higher presentations (83%) followed by regurgitation (58.5%) and a combination of other symptoms in patients. The endoscopic findings, normal esophageal picture in 6 cases, erosive esophagitis different grades in 48 cases, esophageal stenosis in one case, esophageal rings in 6 cases, longitudinal furrows in 5 cases, and white plaques in 20 cases. Other endoscopic findings showed 7 cases with hiatal hernia, 1 case with antral gastritis, 1 case with pangastritis, 2 cases with gastric ulcer, and 2 cases with biliary reflux. Duodenitis was found in 1 case without any duodenal ulcers. Positive campylobacterlike organism (CLO) test was found in 7 cases for H.pylori screening (Table 3).

 

 

Table (3):   Distribution of the studied cases according symptoms, signs and endoscopic findings for all patients

Symptoms

No.

%

Heart burn

44

83.0%

Regurgitation

31

58.5%

Dysphagia

11

20.8%

Heartburn and regurgitation

23

43.4%

Heartburn and dysphagia

4

7.5%

Heartburn, regurgitation, and dysphagia

4

7.5%

Esinophilia

Positive for eosinophilia

47

88.7%

Negative for eosinophilia

6

11.3%

 

Normal esophagus

6

11.3%

Erosive esophagitis (grade la–a)

36

67.9%

Erosive esophagitis (grade la–b)

8

15.1%

Erosive esophagitis (grade la–c)

4

7.5%

Esophageal stenosis

1

1.9%

Hiatus henia

7

13.2%

Esophageal rings

6

11.3%

Longitudinal furrow

5

9.4%

Antral gastritis

20

37.7%

White plaque

1

1.9%

Pangastritis

1

1.9%

Biliary reflux

2

3.8%

Gastric ulcer

4

7.5%

Duodenitis

1

1.9%

Duodenal ulcers

0

0.0%

Positive CLO test

7

13.2%

Negative CLO test

46

86.8%

 

 

 

 

 

 

 

 

     Only 6 cases out of 53 examined endoscopic biopsies have histological features of EoE. The remaining 47 biopsies feature different histological diagnosis included mild reflux esophagitis in 12 cases, moderate reflux esophagitis in 20 cases, and severe reflux esophagitis in 15 cases (Table 4).

 

 

Table (4):   Distribution of the studied cases according to lesion (histopathological diagnosis)

Lesion

No.

%

Esinophilic esophagitis

6

11.3%

Mild reflux esophagitis

12

22.6%

Moderate reflux esophagitis

20

37.7%

Severe reflux esophagitis

15

28.3%

 

 

DISCUSSION

      Esinophilic esophagitis (EoE) is sometimes referred to as “asthma of the esophagus” given that it shares many clinical and pathophysiologic characteristics with asthma (Dellon, 2014). It is defined as a clinicopathologic disorder characterized by ≥ 15 esinophils per high power field (HPF) in one or more esophageal biopsy specimens and the absence of pathologic gastrointestinal reflux disease (GERD) (as evidenced by a normal pH monitoring study or lack of response to adequate acid-suppression therapy) (Dellon, 2011).

     The aim of this study was to evaluate the prevelance of esinophilic esophagitis in atopic patients. This study was carried out on Egyptian asthmatic patients with esophageal symptoms. It included 120 atopic patients. From those patients, only 53 patients had esophageal symptoms (heartburn, regurgitation, or dysphagia). Upper GIT endoscopy was done to all 53 cases and the findings were recorded. Esophageal biopsy was taken from all cases and examined histopathologically for EoE.

The study was divided into two groups: Group (A) included atopic patients without esophageal symptoms (67 cases) and group (B) that included atopic patients with esophageal symptoms (53 cases). In the current study, asthma as a main atopic respiratory disease was chosen and studied to assess the frequency and incidence of EoE in asthmatic patients. The results showed that about 11% of asthmatic patients who suffered from GERD symptoms had associated EoE confirmed by esophageal biopsy and histologic findings. The incidence of EoE increased in atopic asthmatic patients who had high IgE and this observation was matched with that of Mulder et al. (2012). Bronchial asthma is usually associated with esophageal symptoms specially GERD and is considered one of the extraesophageal syndromes of GERD (Carr et al., 2018).

     Our results showed an increase in the prevalence of EoE in men than women (60% men versus 40% women) which was in agreement with Veerappan et al. (2012) who reported that EoE is more prevalent in men than women younger than 50 years. Another study found that the male: female ratio was 4:1. Also, in this study, the most common presenting symptoms of EoE are heartburn, regurgitation, and dysphagia presenting more than 50% of cases (75, 52, 18%, respectively). These results were similar to previous studies which reported that dysphagia was present in 64.0 and 89% of EoE patient (Veerappan et al., 2012). Endoscopic features of EoE may include mucosal edema, concentric rings, longitudinal furrows, strictures, white exudates or plaques, and pallor or decreased vasculature. One study of histologically confirmed EoE by Sgouros et al. (2010) reported that 8.8% of patients had no detectable endoscopic findings of EoE. Mackenzie et al. (2012) found that 42% EoE patients did not have typical findings on endoscopy and might have been missed unless biopsies were taken.

     In the current study, four esophageal mucosal biopsies were taken from each case and this was matched with Nielsen et al. (2014) who document that the recommended least number of biopsies to establish the morphologic diagnosis of EoE are four biopsies and more. The prevalence of EoE in cohort study was 6.5% which is markedly higher than that of an asymptomatic Swedish community by Ronkainen et al. (2010) study. The prevalence in patients with dysphagia (10%) was similar to the prevalence described in other dysphagia populations (10%–15%) in Prasad et al. (2010) study. The significance of the population studied cannot be overstated because these are the patients whom gastroenterologists evaluate daily.

     Another prospective study by Prasad et al. (2010) studied dysphagia patients, identified age, food impaction greater than 5 minutes, endoscopic features of EoE, and use of PPI for GERD as independent risk factors. In previous reports, the prevalence of gastroesophageal reflux disease among asthmatics was reported to be about 30–80% in Balson et al. (2010) and Vincent et al. (2010) studies, which were much higher than that of general population of 10–17%.

     According to the traditional concept, gastroesophageal reflux can cause airway hypersensitivity by direct effect of acid and indirect effect of neural reflex, and also asthma itself can worsen the reflux through intrathoracic negative pressure made by cough and drug-induced lowering of lower esophageal sphincter pressure.

CONCLUSION

     Atopic patients who suffered from esophagitis symptoms should be assessed for EoE by endoscopic and histopathological examination especially if there was a high IgE level or increased blood esinophils.

REFERENCES

  1. Asher WW and Dellon ES. (2014): Esinophilic esophagitis and proton pump inhibitors: controversies and implications for clinical practice. MPH Gastroenterol Hepatol., 10:427–432.
  2. Balson BM, Kravits EKS and McGeady SJ. (2010): Diagnosis and treatment of gastroesophageal reflux in children and adolescents with severe asthma. Ann Allergy Asthma Immunol., 81: 159-164.
  3. Carr S, Chan ES and Watson W. (2018): Esinophilic esophagitis. Allergy Asthma Clin Immunol., 14(2): 58-65.
  4. Cherian S, Smith NM and Forbes DA. (2010): Rapidly increasing prevalence of eosinophylic oesophagi s in western Australia. Arch Dis Child., 91(12): 1000-1004.
  5. Dellon ES. (2011): Approach to diagnosis of esinophilic esophagitis. MPH Gastroenterol Hepatol., 7: 742–744.
  6. Dellon ES. (2014): Diagnostics of esinophilic esophagitis: clinical, endoscopic, and histologic pitfalls. Dig Dis., 32: 48–53.
  7. Furuta GT, Liacouras CA and Collins MH. (2011): First International Gastrointestinal Eosinophil Research Symposium (FIGERS) Subcommittees. Esinophilic esophagitis in children and adults: a systematic review and consensus recommendations for diagnosis and treatment. Gastroenterology, 133:1342–1363.
  8. Mackenzie SH, Go M and Chadwick B. (2012): Esinophilic esophagitis in patients presenting with dysphagia--a prospective analysis. Aliment Pharmacol Ther., 28: 1140–1146.
  9. Monjur A. (2016): Esinophilic esophagitis in adults: an update. World J Gastrointest Pharmacol Ther., 7: 207-213.
  10. Mulder DJ, Mak N, Hurlbut DJ and Justinich CJ. (2012): Atopic and non-atopic esinophilic esophagitis are distinguished by immunoglobulin E-bearing intraepithelial mast cells. Histopathology, 61: 810–822.
  11. Ndraha S. (2010): Frequency scale for the symptoms of GERD score for gastroesophageal reflux disease in Koja Hospital. Indonesian J Gastroenterol Hepatol Dig Endosc., 11: 2-7.
  12. Nielsen JA, Larger DJ, Lewin M, Rendon G and Robert KA. (2014): The optimal number of biopsy fragments to establisha morphologic diagnosis of esinophilic esophagitis. Am J Gastroenterol., 109: 515-520.
  13. Prasad GA, Alexander JA and Schleck CD. (2011): Epidemiology of eosinophylic esophagitis over three decades in Olmsted Country, Minnesota. Clin Gastro-entrol Hepatol., 7: 1055-61.
  14. Prasad GA, Talley NJ and Romero Y. (2010): Prevalence and predictive factors of esinophilic esophagitis in patients presenting with dysphagia: a prospective study. Am J Gastroenterol., 102: 2627–2632.
  15. Rawy AM and Mansour A. (2015): Fraction of exhaled nitric oxide measurement as a biomarker in asthma and COPD compared with local and systemic inflammatory markers. Egypt J Chest Dis Tuberc., 64:13–20.
  16. Ronkainen J, Talley NJ and Aro P. (2010): Prevalence of oesophageal esinophils and esinophilic esophagitis in adults: the population-based Kalixanda study. Gut, 56: 615-620.
  17. Rosner B and Milton RC. (2010): Significance testing for correlated binary outcome data. Biometrics, 44: 505–512.
  18. Sealock RJ, Rendon G and El-Serag HB. (2010): Systemic review: the epedmiology of eosinophylic esophagitis in adults. Aliment Pharmacol Ther., 32: 712-719.
  19. Sgouros SN, Bergele C and Mantides A. (2010): Esinophilic esophagitis in adults: a systematic review. Eur J Gastroenterol Hepatol., 18: 211–217.
  20. Syed AAN, Andrews CN, Shaffer E, Urbanski SJ, Beck P and Storr M. (2012): The risisng incidence of eosinophylic esophagitis is associated with increasing biopsy rates. Alimentary Pharmacol. Ther., 36(10): 950-958.
  21. Trevisani L, Sartori S, Gaudenzi P, Gilli G, Matarese G and Gullini S. (2010): Upper gastrointestinal endoscopy: are preparatory interventions or conscious sedation effective?. A randomized trial. World J Gastroenterol., 10: 3313–3317.
  22. Veerappan GR, Perry JL, Duncan TJ, Baker TP, Maydonovitch C, Lake JM, Wong RK and Osgard EM. (2012): Prevalence of esinophilic esophagitis in an adult population undergoing upper endoscopy: a prospective study. Clinical Gastroenterology and Hepatology, 7(4): 420-6.
  23. Vincent D, Cohn-Jonathan AM, Leport J, Merrouche M, Geronimi A and Pradalier A. (2010): Gastro-oesophageal reflux prevalence and relationship with bronchial reactivity in asthma. Eur Respir J., 10: 2255–2259.



معدل إنتشار إلتهاب المرئ الإزينوفيلي في مرض التحسس بين المرضي المصريين

أحمد عيد صادق، عاصم محمود الشريف، مجدي الدهشان، محمد سامي الحكيم*

قسمي الباطنة العامة والباثولوجيا الاكلينيكية*، كلية الطب، جامعة الأزهر، مصر

E-mail: dr.ahmed_sadek@gmail.com

خلفية البحث: التهاب المريء العصبي هو مرض التهاب المريء التأتبي الذي أصبح يتزايد بشكل متزايد. عادة ما توجد الحمضات في جميع أنحاء الجهاز الهضمي لأنها تتعرض باستمرار للأطعمة والمواد المسببة للحساسية البيئية والسموم ومسببات الأمراض.

الهدف من البحث: تقييم مدى إنتشار التهاب المريء الازينوفيلى لدى مرضى التأتبي.

المرضى وطرق البحث: شملت هذه الدراسة 120 مريضا بالربو تتراوح أعمارهم بين 18-60 عامًا لهذه الدراسة بأثر رجعي غير معشاة، دراسة قائمة على الملاحظة لمركز واحد بأثر رجعي. وتم تقييمهم لأعراض المريء باستخدام مقياس التردد لأعراض مرض الجزر المعدي المريئي (جيرد). وقد تم إجراؤه في عيادة الأمراض الجلدية والأذن والأنف والحنجرة وطب العيون والحساسية بقسم الطب الباطني بمستشفى الحسين الجامعي خلال الفتراة ما بين يوليو 2017 وسبتمبر 2018.

نتائج البحث: كان متوسط  الهيموجلوبيبن المناعي الكلي للمجموعة الثانية أعلى من المجموعة الأولى مع وجود فروق ذات دلالة إحصائية بين المجموعتين. وفيما يتعلق بمتوسط عدد كريات الدم من المجموعة الثانية أعلى من المجموعة الأولى مع وجود فروق ذات دلالة إحصائية بين المجموعتين. توثق الحموضة المعوية أعلى الأعراض (83٪) يليها قلس (58.5٪) ومجموعة من الأعراض الأخرى لدى المرضى. فقط 6 حالات من أصل 53 خزعة بالمنظار تم فحصها لها سمات نسيجية لالتهاب المريء اليوزيني، والـ 47 خزعة المتبقية تتميز بتشخيص نسيجي مختلف شمل إلتهاب المريء الارتجاعي الخفيف في 12 حالة، والتهاب المريء الارتجاعي المعتدل في 20 حالة، وإلتهاب المريء الارتجاعي الشديد في 15 حالة.

الاستنتاج: مرضى الحساسية الذين عانوا من أعراض التهاب المريء يجب تقييمهم من أجل التهاب المريء الازينوفيلى عن طريق الفحص بالمنظار والفحص التشريحي المرضي خاصة إذا كان هناك إرتفاعاً في مستوى الهيموجلوبيبن المناعي أو زيادة الحمضات في الدم.

الكلمات الدالة: إلتهاب المريء العصبي، التأتبي المصري، إلتهاب المريء الازينوفيلى.

  1. REFERENCES

    1. Asher WW and Dellon ES. (2014): Esinophilic esophagitis and proton pump inhibitors: controversies and implications for clinical practice. MPH Gastroenterol Hepatol., 10:427–432.
    2. Balson BM, Kravits EKS and McGeady SJ. (2010): Diagnosis and treatment of gastroesophageal reflux in children and adolescents with severe asthma. Ann Allergy Asthma Immunol., 81: 159-164.
    3. Carr S, Chan ES and Watson W. (2018): Esinophilic esophagitis. Allergy Asthma Clin Immunol., 14(2): 58-65.
    4. Cherian S, Smith NM and Forbes DA. (2010): Rapidly increasing prevalence of eosinophylic oesophagi s in western Australia. Arch Dis Child., 91(12): 1000-1004.
    5. Dellon ES. (2011): Approach to diagnosis of esinophilic esophagitis. MPH Gastroenterol Hepatol., 7: 742–744.
    6. Dellon ES. (2014): Diagnostics of esinophilic esophagitis: clinical, endoscopic, and histologic pitfalls. Dig Dis., 32: 48–53.
    7. Furuta GT, Liacouras CA and Collins MH. (2011): First International Gastrointestinal Eosinophil Research Symposium (FIGERS) Subcommittees. Esinophilic esophagitis in children and adults: a systematic review and consensus recommendations for diagnosis and treatment. Gastroenterology, 133:1342–1363.
    8. Mackenzie SH, Go M and Chadwick B. (2012): Esinophilic esophagitis in patients presenting with dysphagia--a prospective analysis. Aliment Pharmacol Ther., 28: 1140–1146.
    9. Monjur A. (2016): Esinophilic esophagitis in adults: an update. World J Gastrointest Pharmacol Ther., 7: 207-213.
    10. Mulder DJ, Mak N, Hurlbut DJ and Justinich CJ. (2012): Atopic and non-atopic esinophilic esophagitis are distinguished by immunoglobulin E-bearing intraepithelial mast cells. Histopathology, 61: 810–822.
    11. Ndraha S. (2010): Frequency scale for the symptoms of GERD score for gastroesophageal reflux disease in Koja Hospital. Indonesian J Gastroenterol Hepatol Dig Endosc., 11: 2-7.
    12. Nielsen JA, Larger DJ, Lewin M, Rendon G and Robert KA. (2014): The optimal number of biopsy fragments to establisha morphologic diagnosis of esinophilic esophagitis. Am J Gastroenterol., 109: 515-520.
    13. Prasad GA, Alexander JA and Schleck CD. (2011): Epidemiology of eosinophylic esophagitis over three decades in Olmsted Country, Minnesota. Clin Gastro-entrol Hepatol., 7: 1055-61.
    14. Prasad GA, Talley NJ and Romero Y. (2010): Prevalence and predictive factors of esinophilic esophagitis in patients presenting with dysphagia: a prospective study. Am J Gastroenterol., 102: 2627–2632.
    15. Rawy AM and Mansour A. (2015): Fraction of exhaled nitric oxide measurement as a biomarker in asthma and COPD compared with local and systemic inflammatory markers. Egypt J Chest Dis Tuberc., 64:13–20.
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