Nesidioblastosis in Sickle Cell Disease

References

• Kumar A, Posner G, Marsh F, Bellevue R, Dosik H. Acute pancreatitis in sickle cell crisis. J Natl Med Assoc 1989; 81: 91–92
   PubMed Web of Science ®Google Scholar
• Pasquier J M, Bertrand Y, Tran Minh V A, et al. Iconographic rubric. Acute lithiasic pancreatitis, exceptional cause of abdominal pain crisis in sickle cell anemia patient. Arch Fr Prediatr 1991; 48: 353–354
   Google Scholar
• Shehan A G, Machida H, Butzner J D. Acute pancreatitis in a child with sickle cell anemia. J Natl Med Assoc 1993; 85: 70–72
   Google Scholar
• Ziegler D W, Long J A, Philippart A I, Klein M D. Pancreatitis in childhood. Experience with 49 patients. Ann Surg 1988; 207: 257–261
   Google Scholar
• Prinz R A. Mechanisms of acute pancreatitis. Vascular etiology. Int J Pancreatol 1991; 9: 31–38
   PubMedGoogle Scholar
• Pikaranta P, Kivisaari L, Nordling S, Nuutinen P, Schroder T. Vascular changes of pancreatic ducts and vessels in acute necrotizing, and in chronic pancreatitis in humans. Int J Pancreatol 1991; 8: 13–22
   Google Scholar
• Ohri S K, Hashemi M, Keogh B E, Taylor K M. Pancreatic injury after cardiopulmonary bypass. N Engl J Med 1992; 326: 573–574
   Google Scholar
• Addae S K, Odonkor P O. A review of some aspects of endocrine function in sickle cell disease. West Afr J Med 1984; 3: 63–70
   Google Scholar
• Adekile A D, Olusi S O, Oyebola D DO. Oral glucose tolerance test in children with sickle cell anemia. East Afr Med J 1985; 62(3)213–217
   Google Scholar
• Adekile A D, Jegende A O. Juvenile-onset diabetes mellitus in a sickle cell anemia patient. East Afr Med J 1990; 67: 591–593
   Google Scholar
• Okafor L A, Osamo N O. Pancreatic endocrine function in sickle cell anemia. West Afr J Med 1982; 1: 9–12
   Google Scholar
• Saad S T, Braga G S, Saad M J. Decreased C-peptide secretion in sickle cell anemia. Acta Haematol 1989; 82: 81–84
   Google Scholar
• Saad M JA, Saad S TD, Braga G S. Decreased insulin response to glucose in sickle cell trait. Diabetes Metab (Paris) 1991; 17: 69–72
   PubMed Web of Science ®Google Scholar
• Gray N T, Bartlett J M, Kolasa K M, Marcuard S P, Holbrook C T, Horner R D. Nutritional status and dietary intake of children with sickle cell disease. Am J Pediatr Hematol Oncol 1992; 14: 57–61
   PubMedGoogle Scholar
• Odonkor P O. Metabolic and endocrine basis of the growth retardation in sickle cell disease. Bull Eur Physiopathol Respir 1983; 19: 357–359
   Google Scholar
• Singhal A, Davies P, Sahota A, Thomas P W, Serjeant G R. Resting metabolic rate in homozygous sickle cell disease. Am J Clin Nutr 1993; 57: 32–34
   PubMed Web of Science ®Google Scholar
• Bhisitkul D M, Vinik A I, Morrow A L, et al. Prediabetic markers in children with stress hyperglycemia. Arch Pediatr Adolesc Med 1996; 150(9)936–941
   Google Scholar
• Morrison J C, Schneider J M, Kraus A P, Kitabchi A E. The prevalence of diabetes mellitus in sickle cell hemoglobinopathies. J Clin Endocrinol Metab 1979; 48(2)192–195
   Google Scholar
• Reid H L, Photiades D P, Oli J M, et al. Concurrent sickle cell disease and diabetes mellitus. Trop Geogr Med 1988; 40(3)201–4
   Google Scholar
• Boyd Growth E. including reproduction and morphological development. Biological Handbooks, P L Altman, K D Dittmer. Federation of American Societies for Experimental Biology, Washington 1962; 346–348
   Google Scholar
• Oertel J E, Heffess C S, Oertel Y C. Pancreas. Histology for Pathologists, S S Sternberg. Raven Press, New York 1992; 657–663
   Google Scholar
• Albers N, Lohr M, Bogner U, Loy V, Kloppel G. Nesidioblastosis of the pancreas in an adult with persistent hyperinsulinemic hypoglycemia. Am J Clin Pathol 1989; 91: 336–340
   Google Scholar
• Amendt P, Kohnert K D, Kunz J. The hyperinsulinaemic hypoglycaemias in infancy: a study of six cases. Eur J Pediatr 1988; 148: 107–112
   Google Scholar
• Andrews R, Balsitis M, Shurock K, Jeffcoate W J. Nesidioblastosis in adults. Postgrad Med J 1992; 68: 389–390
   Google Scholar
• Arico M, Bianchi E, Zaninetti P, et al. Unusual association of glycogen storage disease type I, nesidioblastosis and possible congenital hypopituitarism. J Inherit Metab Dis 1987; 10: 267–268
   Google Scholar
• Goudswaard W B, Houthoff H J, Koudstaal J, Zwierstra R P. Nesidioblastosis and endocrine hyperplasia of the pancreas: a secondary phenomenon. Hum Pathol 1986; 17: 46–54
   Google Scholar
• Taguchi T, Suita S, Hirose R. Histological classification of nesidioblastosis: efficacy of immunohistochemical study of neuron-specific enolase. J Pediatr Surg 1991; 26: 770–774
   Google Scholar
• Ariel I, Kerem E, Schwartz-Arad D, et al. Nesidiodysplasia—a histologic entity?. Hum Pathol 1988; 19: 1215–1218
   PubMedGoogle Scholar
• Lebo R V, Chakravarti A, Buetow K H, et al. Recombination within and between the human insulin and globin gene loci. Pro Natl Acad of Sci USA 1983; 80: 4808–1412
   Google Scholar
• Nakashima M, Sakamoto N, Umeda F, et al. Point mutation in a family with hyperproinsulinemia detected by single stranded conformational polymorphism. J Clin Endocrinol Metab 1993; 76(3)633–636
   Google Scholar
• Oohashi H, Ohgawara H, Nanjo K, et al. Familial hyperproinsulinemia associated with NIDDM. Diabetes Care 1993; 16(10)1340–1346
   PubMed Web of Science ®Google Scholar
• Faller D V. Vascular modulation. Sickle Cell Disease: Basic Principles and Clinical Practice, S H Embury, R P Hebbel, N Mohandas, M H Steinberg. Raven Press, New York 1994; 235–246
   Google Scholar
• Van Asshe F A. The fetal endocrine pancreas. Carbohydrate Metabolism in Pregnancy and the Newborn, H W Sutterland, J M Stowers. Churchill-Livingstone, Edinburgh 1975; 68
   Google Scholar
• Mostoufi-Zadeh M, Weiss L M, Driscoll S G. Nonimmune hydrops fetalis: a challenge in perinatal pathology. Hum Pathol 1985; 16: 785
   PubMed Web of Science ®Google Scholar
• Jaffe R. The Pancreas. Pediatric Pathology, J T Stocker, L P Dehner. J.B. Lippincott, Philadelphia 1992; vol 2: 791–823
   Google Scholar
• Wellman K F, Volk B W. The islets of infants of diabetic mothers. The Diabetic Pancreas, B W Volk, K F Wellman. Plenum Press, New York 1977; 365
   Google Scholar
• Hultquist G T, Olding L B. Endocrine pathology of infants of diabetic mothers. A quantitative morphological analysis including comparison with infants of isoimmuized and non-diabetic mothers. Acta Endocrinol 1981; 97(suppl 244)1
   Google Scholar
• Kolesnik I UM, Seredenko M M, Abramov A V. Hypoxic training stimulates new growth of pancreatic beta cells and slows development of diabetes mellitus in rats. Doklady Akademii Nauk 1995; 343: 127–129
   Google Scholar