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Biomedical subjects

G Oderda

Publications and source records attributed to G Oderda.

62 records · Page 4Linked to original sources
PubMedDate not supplied

[Yersinia and infantile gastroenteritis].

Fecal samples and intestinal mucosal biopsies of 16 patients in paediatric age, with protracted diarrhoea with blood and mucus, were examined for intestinal pathogens including Yersinia. Yersinia enterocolitica 1/5/XZ and Yersinia intermedia 1/18/XZ were isolated from fecal samples of two patients. In another child, Yersinia enterocolitica, 1/5/XZ was isolated from fecal sample, while Yersinia enterocolitica 1/self-agglutinable/XZ from colon biopsy. The other intestinal pathogens were absent; Aeromonas hydrophila however was isolated from two fecal samples. The Yersinia strains isolated are not frequently found in human infections.

Adolescent↗
PubMedDate not supplied

[Campylobacter pylori and gastroduodenal pathology in children].

Since Warren and Marshall rediscovered in 1983 the presence of a spiral microorganism on the gastric mucosa, and named it Campylobacter Pylori (CP), its significance and characteristics have been largely studied. CP has fulfilled Koch's postulates, which need to proven before a microorganism can be said to cause a disease. The natural source of infection is unknown, but in human volunteer studies, ingestion of a suspension of CP was followed by the development of severe dyspepsia associated with colonization of gastric antrum and histologically proven gastritis B. CP is found overying the gastric epithelium, in the gastric crypts and in the mucus gel layer that protects it from gastric acid. There it causes infiltration of the mucosa by polymorphonuclear leucocytes and mononuclear cells, and mucin depletion. It is found in 60-70% of children with chronic active antral gastritis and can cause various lesions of upper intestinal tract, like esophagitis, duodenitis and gastric or duodenal ulcers. Several tests have been proposed to detect serum antibody against CP, but they are not yet commercially available. Breath test with C 13 or C 14-urea are promising, but up to now the diagnosis can be made only by upper G.I. endoscopy and antral biopsy. A pseudopolypoid antral gastritis seems to be the peculiar lesion caused by CP, but in children it is present only in 40% of cases. CP is easily seen in antral biopsies by Giemsa or Hematoxylin-Eosin staining, or can be cultured in Skirrow's agar under microaerophilic conditions.(ABSTRACT TRUNCATED AT 250 WORDS)

Anti-Bacterial Agents↗
PubMedDate not supplied

[Clinico-histological behavior of celiac patients after gluten load following the definitive diagnosis].

In the last 18 years we have followed 330 children with Coeliac Disease (CD), diagnosed according to the ESPGAN criteria (with 3 jejunal biopsies: during the acute phase, after a gluten-free diet and after a gluten challenge). One to fifteen years after the diagnosis, 61 of them asked to be exposed to a second gluten challenge to see if their intolerance was persistent. Ten percent of them had already started the challenge by themselves, the others were on Gluten Free Diet (GFD). To all 61 serial clinical controls, one-hour-blood-xylose absorption test every three months and a jejunal biopsy was suggested. The jejunal biopsy was performed when symptoms recurred, or when xylose-test showed an impaired absorption, or after 2 years. If the first jejunal biopsy showed a villous atrophy the GFD was restarted, while if a normal mucosa was found the gluten challenge was continued and the jejunal biopsy repeated every year. 52 children (85%) showed a villous atrophy after 1.5 to 72 months. 6 (10%) did not show a clinical or histological relapse, 2 refused the jejunal biopsy because symptomless, and 1 had to restart the GFD because she developed a dermatitis herpetiformis. One-hour-blood-xylose test was performed in 29 children and 20 (69%) showed a low absorbtion, the majority of them in the first year of challenge, and the remaining refused it. 36 of the relapsed children presented with mild clinical symptoms while 16 were symptomless.(ABSTRACT TRUNCATED AT 250 WORDS)

Adolescent↗
PubMedDate not supplied

[Irritable bowel syndrome in children].

The irritable bowel syndrome (IBS) is the most common chronic functional gastroenterological disorder both in adults and in children. In this study we evaluate the different aspects of this syndrome, comparing our observations on 332 children with other studies. Epidemiological data (frequency, sex, age) are examined so as the family histories of gastroenterological disorders. We take in account several pathogenic hypotheses, especially with reference to the alterations of gastrointestinal motility, which could be caused by several factors (psychological, prostaglandins, bile acids, etc.). The clinical picture is very variable, variations depending on the age of children and on the time of onset of IBS. The colic of neonate, caused by retention of air, is the main symptom in the first months of life, followed by chronic diarrhoea, also defined as toddler's diarrhoea, sometime alternating with constipation. In later childhood, recurrent abdominal pain represents a common complaint, in association with diarrhoea or constipation. The principal steps for a proper diagnosis so as the main differential diagnosis are defined. We explain the most important features of management (reassuring parents, free diet), excluding prescription of drugs, that produce only a transitory and symptomatic relief, so as elimination diets, that cause only a failure to thrive without any improvement of symptoms.

Child, Preschool↗
PubMedDate not supplied

[Behavior of pepsin in childhood and its correlation with gastric acid secretion].

Little attention has been given to the gastric secretion of pepsin in children. The purpose of this paper is to define the behaviour of peptic concentration (UI/ml) and Basal (BPO) and Stimulated (SPO) Peptic Outputs in children with normal and altered gastric acid secretion. 54 children, aged 15 months to 12 years, were studied: 20 of them were normal, 20 had gastric hypersecretion and 14 were hyposecretors. In the normal subjects the BPO is inversely correlated with age, while the SPO increases with the body weight, but this increment diminishes after the age of 6 years. From these data one can assume that the gastric principal cells reach their functional maturity around the age of 6 years. In the hypersecretors peptic and acid secretions are not correlated in basal conditions, while after pentagrastrin stimulation peptic secretion is greater than in normal subjects but not as the acid one. The SPO is correlated with body weight and height. The different behaviour of hydrochloric acid and pepsin is probably due to the use of pentagrastrin, which is a specific stimulant of oxyntic but not of principal cells. In the hyposecretors both BPO and SPO are lower than in normal children and no correlation was found with age, body weight and acid secretion.

Age Factors↗
PubMedDate not supplied

[Advantages and limits of rigid rectosigmoidoscope and flexible colonoscope in childhood].

During the past ten years 220 pediatric proctosigmoidoscopies with the rigid instrument in 182 infants and children, and 71 colonoscopies in 62, were performed. Advantages and limits of these two instruments are discussed. The indications and results of the different procedures are presented. Positive diagnoses were obtained in 81% with both techniques while the histological examination was positive in 85% of specimens obtained by colonoscopy and only in 51% of the proctosigmoidoscopical ones. Colonoscopy has increasingly became a complementary method for colonic pathology in children, in comparison with adult medicine, however, pediatric indications have been handled mostly with the shorter instrument for two main reasons: 1) Pediatric colonic pathology affects predominantely the lower tract; 2) Neoplastic lesions, in which total colonoscopy with biopies at different levels is mandatory, are extremely rare in children.

Adolescent↗