摘要:

AbstractThe case of a 13 year old boy with an inflammatory esophagogastric polyp and ulcerative colitis is described. Endoscopy revealed a typical polyp and gastric fold complex at the esophagogastric junction and a hiatal hernia. Histology of a biopsy specimen confirmed an inflammatory polyp covered by hyperplastic squamous and gastric foveolar epithelium. Continuous 24 hour esophageal manometry suggested gastroesophageal reflux, which may be related to the pathogenesis of the lesion. Follow‐up endoscopy showed marked regression of the polyp with medication for reflux eosphagitis. This clinical entity is rare in childhood and adolescence, and the manifestations may not be readily recognized. Therefore, endoscopic biopsy is important in children with esophageal polyps. However, polypectomy is unnecessary except when malignancy is suspected or when symptoms persis

ISSN:1328-8067    

DOI:10.1111/j.1442-200X.1993.tb03006.x

出版商:Blackwell Publishing Ltd    

年代:1993

数据来源: WILEY

摘要:

AbstractWe describe a unique case of a 10 year old girl with dilated cardiomyopathy who has been receiving continuous ambulatory peritoneal dialysis. She responded to treatment with a β1‐agonist. We note that electrocardiography and echocardiography are effective for early recognition of the onset of dilated cardiomyopathy and that a thallium scan should be performed to assess the severity of dilated cardiomyopathy in patients with chronic renal insufficien

ISSN:1328-8067    

DOI:10.1111/j.1442-200X.1993.tb03007.x

出版商:Blackwell Publishing Ltd    

年代:1993

数据来源: WILEY

摘要:

AbstractAn 8 year old girl was admitted to hospital complaining of arthralgia in a few large joints. According to the clinical course and serological tests, a diagnosis of a polyarticular type of juvenile rheumatoid arthritis was made. About 6 weeks after the onset, scoliosis was observed. The curvature regressed spontaneously over the following 6 months.Generally, scoliosis associated with juvenile rheumatoid arthritis has been noted a few years after the onset. A transient scoliosis in the early phase of this disease is rare.

ISSN:1328-8067    

DOI:10.1111/j.1442-200X.1993.tb03008.x

出版商:Blackwell Publishing Ltd    

年代:1993

数据来源: WILEY

摘要:

AbstractAn 18 year old girl with typical clinical features of Williams syndrome suddenly died of intracerebral hemorrhage due to moyamoya disease. Autopsy revealed vascular abnormalities, such as supravalvular aortic stenosis (SAS) and an abnormal complicated cerebrovascular network in the cerebral arteries. The arterial wall of the SAS lesion consisted of thickened medial tissue showing elastic disorganization with prominence of the smooth muscle cells. The narrowed vessels of the circle of Willis showed intimal thickening with an extremely wavy internal elastic lamina and marked thinning of the media. To our knowledge, this is the first report of moyamoya disease associated with Williams syndrome.

ISSN:1328-8067    

DOI:10.1111/j.1442-200X.1993.tb03009.x

出版商:Blackwell Publishing Ltd    

年代:1993

数据来源: WILEY

ISSN:1328-8067    

DOI:10.1111/j.1442-200X.1993.tb03010.x

出版商:Blackwell Publishing Ltd    

年代:1993

数据来源: WILEY

ISSN:1328-8067    

DOI:10.1111/j.1442-200X.1993.tb03011.x

出版商:Blackwell Publishing Ltd    

年代:1993

数据来源: WILEY

ISSN:1328-8067    

DOI:10.1111/j.1442-200X.1993.tb03012.x

出版商:Blackwell Publishing Ltd    

年代:1993

数据来源: WILEY

ISSN:1328-8067    

DOI:10.1111/j.1442-200X.1993.tb03013.x

出版商:Blackwell Publishing Ltd    

年代:1993

数据来源: WILEY