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Nesidioblastosis with necrotising enterocolitis: an enigma
Pediatric Surgery International, 2000Necrotising 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
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Nesidioblastosis in Sickle Cell Disease
Fetal and Pediatric Pathology, 2001Although the endocrine pancreas appears to play an important role in the pathophysiology of sickle cell disease, very little is known about the morphologic changes in this tissue. Our study was initiated to delineate the microscopic features of the endocrine pancreas in a large autopsy series of sickle cell hemoglobinopathies.
D E, Culberson +6 more
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Surgical Treatment of Nesidioblastosis in Childhood
1991A 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
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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
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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
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Nesidioblastosis of the Pancreas
American Journal of Clinical Pathology, 1990D, Kumar, N E, Warner, T L, Fong
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[Experiences with nesidioblastosis].
Zentralblatt fur Chirurgie, 1991Highly 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
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[Nesidioblastosis and persistent neonatal hyperinsulinism].
Journees annuelles de diabetologie de l'Hotel-Dieu, 1995Neonatal 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
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