Results 171 to 180 of about 1,752 (196)
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Surgical treatment of nesidioblastosis

Pediatric Surgery International, 1986
This report comprises ten children with hyperinsulinaemic hypoglycaemia who did not respond to medical management and required surgical treatment. Eight were infants under the age of 1 year while two were children aged 3.5 and 5 years, respectively.
L. Spitz   +4 more
openaire   +1 more source

Nesidioblastosis with necrotising enterocolitis: an enigma

Pediatric Surgery International, 2000
Necrotising enterocolitis with nesidioblastosis is a rare, lethal coexistence during the newborn period. We report this unusual combination leading to surgery: a partial pancreatectomy and resection with primary anastomosis, and discuss the dilemma of the procedure of choice during therapy.
M S, Kulkarni, V A, Upadhyay
openaire   +2 more sources

[Experiences with nesidioblastosis].

Zentralblatt fur Chirurgie, 1991
Highly differentiated processes relating to insulin-generating cells of the endocrine pancreas are covered by the term of nesidioblastosis. The disease is primarily characterised by persistent hypoglycaemia, and it affects newborns and young infants. Diffuse nesidioblastosis is predominant, as compared to focal processes.
E, Gottschalk   +3 more
openaire   +1 more source

Nesidioblastosis in Adults Without Insular Hyperfunction

American Journal of Clinical Pathology, 1982
Examination of pancreases from a series of 207 autopsies of adults without either clinical or autopsy evidence of insular hyperfunction showed minimal nesidioblastosis in 36.7%. Ductulo-insular complexes, together with insular cells among the acini, were found in 10.6% of the biopsy specimens.
openaire   +2 more sources

Nesidioblastosis in adults.

Israel journal of medical sciences, 1989
A 75-year-old woman with hyperinsulinemic hypoglycemia who died of acute myocardial infarction with ventricular rupture is reported. The microscopic examination of the pancreas revealed that the cause of hyperinsulinemic hypoglycemia was nesidioblastosis characterized by the presence of enlarged, irregular islets of Langerhans and clusters of islet ...
A, Chines   +3 more
openaire   +1 more source

Surgical Treatment of Nesidioblastosis in Childhood

1991
A review of the literature on the surgical treatment of nesidioblastosis in childhood was made to answer the following questions: age at operation, surgical procedure, pathohistological findings, incidence of recurrence and its treatment, as well as mortality. Primary subtotal pancreatectomy appears to be the method of choice. It should be performed as
J, Dobroschke, R, Linder, A, Otten
openaire   +2 more sources

[Nesidioblastosis and persistent neonatal hyperinsulinism].

Journees annuelles de diabetologie de l'Hotel-Dieu, 1995
Neonatal hyperinsulinism is characterized by severe hypoglycaemia which can cause serious neurologic effects. Pancreatic morphological abnormalities involve either focal or diffuse lesions. The former can be cured by resection, whereas the latter, of uncertain pathogenesis, often require subtotal pancreatectomy. We investigated various hypotheses in an
C, Sempoux   +5 more
openaire   +2 more sources

[Surgical therapy of nesidioblastosis].

Zeitschrift fur Kinderchirurgie : organ der Deutschen, der Schweizerischen und der Osterreichischen Gesellschaft fur Kinderchirurgie = Surgery in infancy and childhood, 1984
Whereas today intensive-paediatric management of the acute, life-threatening situation in organically conditioned hypoglycaemias is quite successful, conservative long-term treatment of nesidioblastosis is still unsatisfactory with regard to the prevention of subsequent cerebral damage.
W, Saul, B, Willberg, H J, Bremer
openaire   +1 more source

[Familial nesidioblastosis].

Monatsschrift fur Kinderheilkunde, 1980
F K, Trefz   +4 more
openaire   +3 more sources

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