Eosinophilic gastroenteritis

A rare benign gastrointestinal disease characterized by the presence of abnormal and nonspecific gastro-intestinal (GI) manifestations, associated with an eosinophilic infiltration of the GI tract, which can affect several segments and involve several layers within the GI wall.



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Narrow down the case reports



Total: 359 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
13
(38.8%)
1631359
[Eosinophilia and ascites as an expression of a subserous form of eosinophilic gastroenteritis].
Sanchez-Fayos MP, Miranda R, Renedo L, Porres JC, Hernandez Guio C.
Rev Clin Esp. 1992;191(1):30-4.
Ascites Eosinophilia Pleural effusion
Ascites Eosinophilia Females Gastroenteritis Homo sapiens Middle Aged Peritonitis
13
(38.8%)
1380204
Interleukin-5 in eosinophilic gastroenteritis.
Takahashi T, Nakamura K, Nishikawa S, Tsuyuoka R, Suzuki A, Murakami M, Amenomori M, Okuno Y, Imura H.
Am J Hematol. 1992;40(4):295-8.
Ascites Eosinophilia Pleural effusion
CSF2 CSF3 IL3 IL5
Adult Antibodies Bone Marrow Bone Marrow Cells Cultured Cells Enzyme-Linked Immunosorbent Assay Eosinophilia Females Gastroenteritis Granulocyte Colony-Stimulating Factor Granulocyte-Macrophage Colony-Stimulating Factor Homo sapiens
13
(38.8%)
1344929
[Eosinophilic ascites. 2 new case reports].
Durieu I, Nove-Josserand R, Cathebras P, Durand DV, Rousset H, Levrat R.
Rev Med Interne. 1992;13(6):446-8.
Pleural effusion Eosinophilic ascites Hypereosinophilia
Age Factors Ascites Eosinophilia Females Gastrointestinal Diseases Homo sapiens Hypersensitivity Male Middle Aged Sex Factors
24
(38.2%)
9715385
[Recurrent angioedema with gastroenteritis in blood and tissue eosinophilia].
Schultz ES, Diepgen TL, Schuler G, von den Driesch P.
Hautarzt. 1998;49(7):566-70.
Eosinophilia Angioedema
Adult Angioedema Biopsy Eosinophilia Gastroenteritis Homo sapiens Intestinal Mucosa Male Skin
25
(38.2%)
27554385
Hemangioma of the rectum - How misleading can hematochezia be?
Vitor S, Oliveira Ferreira A, Lopes J, Velosa J.
Rev Esp Enferm Dig. 2016;108(8):500-1.
Hemangioma Iron deficiency anemia Hematochezia
Gastrointestinal Hemorrhage Hemangioma, Cavernous Homo sapiens Magnetic Resonance Imaging Male Rectal Neoplasms
26
(37.5%)
21160800
Enterolithiasis complicating eosinophilic enteritis: A case report and review of literature.
Shivathirthan N, Maheshwari G, Kamath D, Haldar P.
World J Gastrointest Surg. 2009;1(1):68-70.
Anemia Abdominal pain
26
(37.5%)
456850
Eosinophilic gastroenteritis in extreme allergy. Immunopathological comparison with nonallergic gastrointestinal disease.
Caldwell JH, Sharma HM, Hurtubise PE, Colwell DL.
Gastroenterology. 1979;77(3):560-4.
Eosinophilia Iron deficiency anemia Protein-losing enteropathy
Gastroenteritis Homo sapiens Hypersensitivity Immunocytoadherence Immunoglobulin E Lymphocyte Activation Male
28
(37.4%)
1981780
Eosinophilic gastroenteritis with eosinophilic ascites: report of a case.
Tai YG, Liu JD, Lin KY, Chang JG, Wang CK, Siauw CP, Chen PH.
J Formos Med Assoc. 1990;89(10):901-4.
Urticaria Ascites Eosinophilia
Adult Ascites Eosinophilia Gastroenteritis Homo sapiens Male
29
(37.1%)
29434146
(6064693)
Eosinophilic Gastroenteritis in Which Obstructive Jaundice Developed due to Invagination of the Duodenal Wall.
Hamamoto H, Hashimoto S, Taguchi H, Kojima I, Kasai A, Tsuneyoshi K, Kuwazuru K, Arima S, Kanmura S, Ido A.
Intern Med. 2018;57(13):1841-1847.
Jaundice Eosinophilia
Adult Duodenum Females Gastroenteritis Homo sapiens Jaundice, Obstructive Male Middle Aged Steroids X-Ray Computed Tomography Young Adult
29
(37.1%)
16917405
Eosinophilic gastroenteritis of the pancreas: an unusual cause of obstructive jaundice.
Sheth A, Palmer R, Jordan PA, Manas K, Bhalodia A.
J Clin Gastroenterol. 2006;40(7):623-5.
Jaundice Eosinophilia
Endoscopic Retrograde Cholangiopancreatography Eosinophilia Gastroenteritis Homo sapiens Jaundice, Obstructive Male Middle Aged Pancreatic Diseases Pancreatic Pseudocyst Pathological Dilatation X-Ray Computed Tomography
        

Phenotype(s) retrieved from Orphanet

    Total: 22

HPO ID Term Frequency
HP:0001880 Eosinophilia Very frequent (99-80%)
HP:0001903 Anemia Frequent (79-30%)
HP:0001974 Leukocytosis Frequent (79-30%)
HP:0002013 Vomiting Frequent (79-30%)
HP:0002014 Diarrhea Frequent (79-30%)
HP:0002015 Dysphagia Frequent (79-30%)
HP:0002024 Malabsorption Frequent (79-30%)
HP:0002027 Abdominal pain Frequent (79-30%)
HP:0002570 Steatorrhea Frequent (79-30%)
HP:0003073 Hypoalbuminemia Frequent (79-30%)
HP:0003193 Allergic rhinitis Frequent (79-30%)
HP:0011024 Abnormality of the gastrointestinal tract Frequent (79-30%)
HP:0011227 Elevated C-reactive protein level Frequent (79-30%)
HP:0500014 obsolete Abnormal test result Frequent (79-30%)
HP:0000969 Edema Occasional (29-5%)
HP:0001047 Atopic dermatitis Occasional (29-5%)
HP:0001541 Ascites Occasional (29-5%)
HP:0001824 Weight loss Occasional (29-5%)
HP:0002099 Asthma Occasional (29-5%)
HP:0002243 Protein-losing enteropathy Occasional (29-5%)
HP:0002573 Hematochezia Occasional (29-5%)
HP:0003565 Elevated erythrocyte sedimentation rate Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 88

HPO ID Term # of case reports
HP:0001880 Eosinophilia 57
HP:0001541 Ascites 35
HP:0002027 Abdominal pain 18
HP:0002014 Diarrhea 13
HP:0012393 Allergy 13
HP:0002099 Asthma 11
HP:0031780 Eosinophilic ascites 9
HP:0005214 Intestinal obstruction 8
HP:0500093 Food allergy 8
HP:0002013 Vomiting 7
HP:0002024 Malabsorption 5
HP:0001733 Pancreatitis 4
HP:0001891 Iron deficiency anemia 4
HP:0002243 Protein-losing enteropathy 4
HP:0002588 Duodenal ulcer 4
HP:0002595 Ileus 4
HP:0001082 Cholecystitis 3
HP:0001735 Acute pancreatitis 3
HP:0001824 Weight loss 3
HP:0002018 Nausea 3
HP:0002021 Pyloric stenosis 3
HP:0002202 Pleural effusion 3
HP:0002576 Intussusception 3
HP:0004387 Enterocolitis 3
HP:0005263 Gastritis 3
HP:0410281 Dyspepsia 3
HP:0000969 Edema 2
HP:0001903 Anemia 2
HP:0001945 Fever 2
HP:0002028 Chronic diarrhea 2
HP:0002090 Pneumonia 2
HP:0002248 Hematemesis 2
HP:0002583 Colitis 2
HP:0002586 Peritonitis 2
HP:0002592 Gastric ulcer 2
HP:0011458 Abdominal symptom 2
HP:0031368 Intestinal perforation 2
HP:0031370 Small intestinal perforation 2
HP:0032061 Hypereosinophilia 2
HP:0100665 Angioedema 2
HP:0000099 Glomerulonephritis 1
HP:0000819 Diabetes mellitus 1
HP:0000952 Jaundice 1
HP:0000964 Eczema 1
HP:0001025 Urticaria 1
HP:0001081 Cholelithiasis 1
HP:0001271 Polyneuropathy 1
HP:0001279 Syncope 1
HP:0001324 Muscle weakness 1
HP:0001370 Rheumatoid arthritis 1
HP:0001433 Hepatosplenomegaly 1
HP:0001508 Failure to thrive 1
HP:0001744 Splenomegaly 1
HP:0001907 Thromboembolism 1
HP:0002019 Constipation 1
HP:0002043 Esophageal stricture 1
HP:0002254 Intermittent diarrhea 1
HP:0002571 Achalasia 1
HP:0002573 Hematochezia 1
HP:0002664 Neoplasm 1
HP:0002716 Lymphadenopathy 1
HP:0002721 Immunodeficiency 1
HP:0002835 Aspiration 1
HP:0003073 Hypoalbuminemia 1
HP:0003124 Hypercholesterolemia 1
HP:0003193 Allergic rhinitis 1
HP:0005202 Helicobacter pylori infection 1
HP:0006515 Interstitial pneumonitis 1
HP:0006560 Biliary hyperplasia 1
HP:0008751 Laryngeal cleft 1
HP:0009831 Mononeuropathy 1
HP:0012819 Myocarditis 1
HP:0025289 Cervical lymphadenopathy 1
HP:0025428 Bronchospasm 1
HP:0030151 Cholangitis 1
HP:0030731 Carcinoma 1
HP:0031274 Hypovolemic shock 1
HP:0032155 Abdominal cramps 1
HP:0032252 Granuloma 1
HP:0100021 Cerebral palsy 1
HP:0100279 Ulcerative colitis 1
HP:0100537 Fasciitis 1
HP:0100614 Myositis 1
HP:0100633 Esophagitis 1
HP:0100827 Lymphocytosis 1
HP:0200123 Chronic hepatitis 1
HP:0410019 Epigastric pain 1
HP:0410151 Eosinophilic infiltration of the esophagus 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID