Observations on the Chloride Metabolism in Congenital Pyloric Stenosis.
نویسندگان
چکیده
A fall in the chloriine content of the blood in cases of high intestiiial obstruction is a well-recognized biochemical finding. The opinion is genierally held that the diminution in the level of the blood chlorine is due primarily to the loss of chlorine by the vomitus. Accompanying this decrease in chlorine there is ani increase in the CO2 content, resulting in a non-gaseouis alkalosis ww ith a diminution in the respiratory exchange. This increase in CO2 Mould appear to be the result of the body's effort to maintain the ionic concentration of the blood at the normal level, and simultaneously, to compensate the deficienicy in the acid radicle. Very strong experimental proof has been brought forward by Gamblel and others in favour of the truth of this hypothesis. In a previous communication2 we have shown that the blood chlorine tends to be low in congenital pyloric stenosis, the diminution being roughly related to the severity of the vomiting. But we have seen cases in which there was present a typical picture of alkalosis, as indicated by the raised blood CO2 content and the depressed breathing, either duiring a period in which no vomiiitinig occurred or, as in one instance, when there u-as a complete absenlce of vomiting. In Table 1 examples are given in which the depressed breathing was a feature despite the comparatively normal valuie for the blood chlorine. lIncidenitally, it shows that there is iiot necessarily a correlation betweeni the
منابع مشابه
Congenital Hypertrophic Pyloric Stenosis: A Case Report
Background Hypertrophic pyloric stenosis (HPS) is a common surgical condition in infancy, and typically presents at 2-4 weeks of age. Case Presentation A full term male neonate in Zeinabieh hospital, Shiraz, Iran was presented with oral feeding intolerance from birth, bile-stained...
متن کاملFirst Report of A Unique Presentation of Hypertrophic Pyloric Stenosis Following Type I Esophageal Atresia; A Case Report
Combination of congenital esophageal atresia and subsequent hypertrophic pyloric stenosis is a rare condition which occurs in early infancy. The underlying etiology and pathophysiology of this association still remains unclear. In this paper we report a unique case of hypertrophic pyloric stenosis, for the first time, which occurred in an infant who underwent surgery for type I esophag...
متن کاملHypertrophic pyloric stenosis in infants: is it a congenital or acquired disorder? Reflections on 2 cases
Based on evidence from two collected and treated clinical observations of hypertrophic pyloric stenosis in children of 5 and 12 months of age, the authors give their point of view on the unresolved issue of the etiology of hypertrophic pyloric stenosis. They emphasize that there are more and more factors to prove this is an acquired condition.
متن کاملEpidermolysis Bullosa associated with pyloric stenosis: A case report
Epidermolysis bullosa are a group of hereditary skin diseases manifested as blisters on the sites of trauma to the skin. According to the level of blister development, epidermolysis bullosa are divided into the following groups: epidermolysis bullosa simplex, junctional epidermolysis bullosa and dystrophic epidermolysis bullosa. The latter two groups are associated with poorer prognosis and hig...
متن کاملPyloric stenosis: congenital or acquired?
Pyloric muscle dimensions were measured in 1400 consecutive newborn infants. Nine of these subsequently developed pyloric stenosis. Their pyloric measurements at birth were all within the normal range. Congenital preformed muscular hypertrophy does not appear to be present in babies who later develop pyloric stenosis.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Archives of disease in childhood
دوره 6 31 شماره
صفحات -
تاریخ انتشار 2007