Pankreaserkrankungen im Säuglingsalter

Burghard, Erich

doi:10.1007/bf01721401

Cited by 8 publications

(2 citation statements)

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“…The cases reported by Clarke and Hadfield (1924), by Burghard (1925), Passini (1919, and Gross (1926) are all similar to those reported here. Julius Hess and Saphir (1935) have recently reported three cases which they call ' coeliac disease.'…”

Section: Post-mortem Lesions Of the Pancreas Aresupporting

confidence: 88%

“…Burghard (1925) points out the difference between the histological appearances in those cases which occur in adults caused by obstruction to the excretory ducts and the dilatation and distortion of the ducts which were present in his case and in some of those reported here. He considers that this condition is a congenital one due to failure of normal development of the pancreas.…”

Section: Post-mortem Lesions Of the Pancreas Arementioning

confidence: 51%

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Congenital steatorrhoea due to pancreatic defect

Harper¹

1938

Archives of Disease in Childhood

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Section: Post-mortem Lesions Of the Pancreas Aresupporting

confidence: 88%

Section: Post-mortem Lesions Of the Pancreas Arementioning

confidence: 51%

Congenital steatorrhoea due to pancreatic defect

Harper¹

1938

Archives of Disease in Childhood

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Cystic Fibrosis of the Pancreas and Its Relation to Celiac Disease

Andersen¹

1938

Am J Dis Child

1,054

392

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The pathology and pathologic physiology of celiac disease remain obscure in spite of the many attempts that have been made to understand them. It has become clearer in recent years that celiac disease is a clinical picture "characterized by arrest of growth, a distended abdomen, and attacks of diarrhoea with large, pale, foul-smelling stools" 1 rather than a disease entity and that the underlying pathologic condition may differ in different cases.2 A tradition exists that pancreatic steatorrhea can be readily differentiated from idiopathic steatorrhea by the low percentage of split fat in the stools associated with the former and the normal percentage characterizing the latter. A careful survey of the literature, however, reveals few cases of either disease in which careful clinical observations have been followed by adequate postmortem examination. The present study was initiated because of the findings in case 44 (XX), in which a patient with celiac disease who had a high percentage of split fat in the stools and who had responded favorably to treatment for celiac disease was found at autopsy to have cystic fibrosis of the pancreas. This demonstrated that the recognized criteria of differentiation between the steatorrhea due to pancreatic insufficiency and that due to other causes are unreliable.To establish more reliable criteria it is necessary to study cases in which normal acinar tissue has been proved by postmortem examination to be absent or inadequate and to compare them with cases of celiac disease associated with a normal pancreas. The plan of the present investigation has been to collect the cases in which pancreatic insuffi¬ ciency has been proved by microscopic examination of the pancreas, to

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Pathologie der Bauchspeicheldrüse (Mit Ausnahme der Langerhansschen Inseln und der Diabetesfrage.)

Gruber¹

1929

Verdauungsdrüsen

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Pankreaserkrankungen im Säuglingsalter

Cited by 8 publications

References 1 publication

Congenital steatorrhoea due to pancreatic defect

Congenital steatorrhoea due to pancreatic defect

Cystic Fibrosis of the Pancreas and Its Relation to Celiac Disease

Pathologie der Bauchspeicheldrüse (Mit Ausnahme der Langerhansschen Inseln und der Diabetesfrage.)

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