[Hypertrophic pyloric stenosis].
نویسندگان
چکیده
Sir, I should like to report a case of hypertrophic pyloric stenosis presenting at the age of 2 years 6 months. This male, only child was admitted with a 5-day history of fever and vomiting, which was not bile stained. His past history was normal and he had not vomited in infancy. The vomiting settled within two days and he was discharged to be readmitted 8 days later with a recurrence of his symptoms. The vomiting had become projectile. An abdominal radiograph again showed a gas-distended stomach with residue, suggesting gastric outlet obstruction. Barium meal revealed a narrow pyloric canal which was confirmed by endoscopy. Surgery showed a thick-walled stomach and a pyloric tumour typical ofhypertrophic pyloric stenosis. A coincidental finding was a thick band from the junction of the first and second parts of the duodenum kinking the duodenum at this point and holding up the first part onto the under surface of the liver. There was no evidence of duodenal obstruction or of malrotation. A Ramstedt pyloromyotomy was performed and the band divided. 'Congenital' or 'infantile' hypertrophic pyloric stenosis usually presents in the first weeks of life, symptoms beginning at an average age of 3.5 weeks.' Although the literature contains reports of several older infants presenting with this condition,2'3 it is extremely rare for it to present in children. Hypertrophic pyloric stenosis presenting after thoracic surgery in a boy aged 3 years 6 months has been described.3 These authors2'3 have also found difficulties with diagnosing late onset pyloric stenosis, including reluctance to consider the diagnosis in an older infant or child and episodic presentation with periods of remission. The duodenal band was considered to be a coincidental congenital anomaly and unrelated to the pyloric stenosis. Late presentation of pyloric stenosis is rare but should be considered in the differential diagnosis for older children presenting with recurrent vomiting and weight loss, even if the history is of relatively short duration.
منابع مشابه
First 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 کاملCongenital 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 کاملIdiopathic hypertrophic pyloric stenosis combined with left paraduodenal hernia in an adult.
OBJECTIVE We report a case of primary hypertrophic pyloric stenosis combined with a paraduodenal hernia in a 35-year-old woman. CLINICAL PRESENTATION AND INTERVENTION The patient presented with signs of obstructive ileus. CT of the abdomen revealed a marked dilatation of the stomach and the proximal jejunum as well as a circumferential thickening of the antral-pyloric region with characterist...
متن کاملمقایسه نتایج درمان با آتروپین سولفات و پیلورومیوتومی در شیرخواران مبتلا به استنوز هیپرتروفیک پیلور
Background & Aims: In hypertrophic pyloric stenosis (HPS) the hypertrophied muscles of pylorus cause partial gastric outlet obstruction. The standard management of HPS is pyloromyotomy. However, successful treatment of HPS with atropine sulfate also has been reported. We aim to compare the outcomes of medical and surgical treatment for HPS. Materials & Methods: In this comparative clinical tri...
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ورودعنوان ژورنال:
- Surgery, gynecology & obstetrics
دوره 86 1 شماره
صفحات -
تاریخ انتشار 1948