3.Recurrent abdominal pain, peritoneal effusion, and eosinophilia in a boy aged 17 years.
Kun YANG ; Rong-Hua LUO ; Yi-Lai SUN
Chinese Journal of Contemporary Pediatrics 2021;23(11):1169-1173
A boy, aged 17 years, was admitted again due to abdominal pain, diarrhea, and eosinophilia for 3 years, which worsened for 3 days. Three years ago, the boy suffered from abdominal pain and diarrhea after eating yogurt; color Doppler ultrasound showed a large amount of peritoneal effusion, and routine blood test, bone marrow cell morphology, and ascites histological examination showed a large number of eosinophils. Three days ago, he was admitted again due to abdominal pain and diarrhea. The gastrointestinal endoscopy showed eosinophil infiltration in the angle of stomach. The boy was diagnosed with eosinophilic gastrointestinal disease (eosinophilic gastroenteritis). He was improved after the treatment with glucocorticoids and dietary avoidance, and no recurrence was observed during the one-year follow-up. It is concluded that for children who attend the hospital due to gastrointestinal symptoms such as abdominal pain and diarrhea, if there is an increase in peripheral blood eosinophils, it is necessary to consider the possibility of eosinophilic gastrointestinal disease, and eosinophil infiltration and abnormal eosinophil count in gastrointestinal tissue based on endoscopic biopsy may be the key to diagnosis.
Abdominal Pain/etiology*
;
Ascitic Fluid
;
Enteritis
;
Eosinophilia/etiology*
;
Gastritis
;
Humans
;
Male
4.Foodborne Eosinophilia due to Visceral Larva Migrans: A Disease Abandoned.
Journal of Korean Medical Science 2012;27(1):1-2
No abstract available.
Animals
;
Eosinophilia/*etiology
;
Humans
;
Larva Migrans, Visceral/*complications/diagnosis/epidemiology
;
Prevalence
;
Toxocara canis/isolation & purification
5.Cigarette Smoking-Induced Acute Eosinophilic Pneumonia: A Case Report Including a Provocation Test.
Gene Hyun BOK ; Yang Ki KIM ; Young Mok LEE ; Ki Up KIM ; Soo Taek UH ; Jung Hwa HWANG ; Dong Won KIM
Journal of Korean Medical Science 2008;23(1):134-137
The mechanism and cause of acute eosinophilic pneumonia are largely unknown. Many factors including the smoking of cigarettes have been suggested, but none have been proven to directly cause acute eosinophilic pneumonia. The authors report a case of acute eosinophilic pneumonia in a young Asian male who recently started smoking. The diagnosis was made based on his clinical course and results of chest radiography, lung spirometry, bronchoalveolar lavage, and transbronchial lung biopsies. After administration of methylprednisolone, his clinical course rapidly improved. A provocation test was designed to establish a connection between cigarette smoking and the development of acute eosinophilic pneumonia. After the provocation test, the patient showed identical symptoms, increase in sputum eosinophils, and worsening of pulmonary function. The results of the provocation test suggest that smoking may directly cause acute eosinophilic pneumonia, and support previous reports of cigarette smoking-induced acute eosinophilic pneumonia.
Acute Disease
;
Adolescent
;
*Bronchial Provocation Tests
;
Humans
;
Male
;
Pulmonary Eosinophilia/*etiology/physiopathology
;
Smoking/*adverse effects
6.Eosinophilia due to osteomyelitis in a dog.
Seifollah N DEHGHANI ; Shahin HAJIGHAHRAMANI
Journal of Veterinary Science 2005;6(3):255-257
A dog with a lesion in the left elbow area and presence of purulent materials was referred to hospital;history, clinical examination, laboratory test and radiological evaluation of the dog proved the presence of osteomyelitis. Eosinophilia was evident by haematologic test. Intensive antibiotic, anti-inflammatory medication, local wound management and restricted physical activity, improved osteomelitis condition and reduced eosinophil number. Therefore it seemed that osteomyelitis was the cause of eosinophilia in this dog.
Animals
;
Dog Diseases/*blood/therapy
;
Dogs
;
Eosinophilia/etiology/*veterinary
;
Male
;
Osteomyelitis/complications/*veterinary
7.Recurrent ascites as a presenting manifestation of eosinophilic gastroenteritis: a case report.
Mei CHEN ; Li-Li LU ; Zhi-Chun FENG
Chinese Journal of Contemporary Pediatrics 2011;13(3):265-266
Ascites
;
etiology
;
Child, Preschool
;
Enteritis
;
complications
;
Eosinophilia
;
complications
;
Female
;
Gastritis
;
complications
;
Humans
;
Recurrence
8.A Patient with Eosinophilic Gastroenteritis Presenting with Acute Pancreatitis and Ascites.
Moon Seong BAEK ; Young Mi MOK ; Weon Cheol HAN ; Yong Sung KIM
Gut and Liver 2014;8(2):224-227
Eosinophilic gastroenteritis (EGE) is a rare disease characterized by focal or diffuse eosinophilic infiltration of the gastrointestinal tract, especially the stomach and duodenum. EGE has vague, nonspecific symptoms, including nausea, vomiting, abdominal pain, diarrhea, weight loss, ascites, and malabsorption. Here, we report a patient with EGE presenting with concurrent acute pancreatitis and ascites. A 68-year-old woman was admitted with abdominal pain, nausea, vomiting, and watery diarrhea. Laboratory findings revealed elevated serum titers of amylase, lipase, and peripheral blood eosinophil count. An abdominopelvic computed tomography scan showed a normal pancreas, moderate amount of ascites, and duodenal thickening. A esophagogastroduodenoscopy showed patchy erythematous mucosal lesions in the 2nd portion of the duodenum. Biopsies from the duodenum indicated eosinophilic infiltration in the lamina propria. The patient was successfully treated with prednisolone and montelukast. Despite its unusual occurrence, EGE may be considered in the differential diagnosis of unexplained acute pancreatitis, especially in a patient with duodenal edema on imaging or peripheral eosinophilia.
Acute Disease
;
Aged
;
Ascites/*etiology
;
Enteritis/*complications
;
Eosinophilia/*complications
;
Female
;
Gastritis/*complications
;
Humans
;
Pancreatitis/*etiology
;
Tomography, X-Ray Computed
9.A global perspective in asthma: from phenotype to endotype.
Chinese Medical Journal 2013;126(1):166-174
Asthma
;
drug therapy
;
epidemiology
;
etiology
;
China
;
epidemiology
;
Cluster Analysis
;
Humans
;
Phenotype
;
Pulmonary Eosinophilia
;
etiology
;
Smoking
;
adverse effects
;
Th2 Cells
;
immunology
10.Recurrent fever, hepatosplenomegaly and eosinophilia in a boy.
Dan LIU ; Li-Li ZHONG ; Yun LI ; Min CHEN
Chinese Journal of Contemporary Pediatrics 2016;18(11):1145-1149
A 2-year-old boy was admitted into the hospital because of cough and fever. Lymph node tuberculosis was noted when he was 2 months old and he was subsequently hospitalized several times because of cough and fever. After hospitalization the laboratory examination showed an increased eosinophia level in blood. The immune function tests shows decreased levels of IgG, IgA, and IgM. The patient had no response to anti-tuberculosis, anti-bacterial, and anti-fungal treatment, resulting in recurrent fever and progressive enlargement of the liver and spleen. Jam-like stools were noted 35 days after admission. B ultrasonography showed suspected intussusception. Laparotomy, reduction of intussusception and ileocecum angioplasty, biopsies of intestinal wall nodules and lymphoglandulae mesentericae, and hepatic biopsy were then performed under general anesthesia. The patient eventually died because of postoperative severe liver damage, disseminated intravascular coagulation and electrolyte disorder. Both the blood culture and hepatic biopsy tests showed Penicillium marneffei infecton. Immunodeficiency gene test was performed on the patient, his bother and their parents. T→G base substitution mutation (IVS1-3 T→G) in the CD40L gene was found in the patient. X-linked hyper-IgM syndrome was thus diagnosed in the patient. His mother was a carrier of the mutated CD40L gene, but his father was normal in the gene test. Hemizygous mutation in the CD40L gene was found in both the patient and his bother.
CD40 Ligand
;
genetics
;
Child, Preschool
;
Eosinophilia
;
etiology
;
Fever
;
etiology
;
Hepatomegaly
;
etiology
;
Humans
;
Hyper-IgM Immunodeficiency Syndrome
;
diagnosis
;
genetics
;
Male
;
Mutation
;
Recurrence
;
Splenomegaly
;
etiology