Ultrastructural aspects of enterocyte defects in infancy and childhood

Ultrastructural Pathology

Volumn 34, Issue 3, 2010, Pages 117-125

  Iancu, Theodore C ^a   Manov, Irena ^a  

^a TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

Author keywords

Celiac disease; Congenital defects of glycosylation; Electron microscopy; Enterocyte defects; Lymphangectasia; Malabsorption syndromes; Microvillus inclusion disease; Steatorrhea

Indexed keywords

CELIAC DISEASE; CELL INCLUSION; CHILD; CONFERENCE PAPER; CYTOMEGALOVIRUS INFECTION; ENTEROPATHY; HUMAN; INFANT; INFANTILE DIARRHEA; INTESTINE CELL; INTESTINE LYMPHANGIECTASIA; INTESTINE MUCOSA; METHODOLOGY; MICROVILLUS; NEWBORN; PATHOLOGY; PRESCHOOL CHILD; SMALL INTESTINE; STEATORRHEA; TRANSMISSION ELECTRON MICROSCOPY; ULTRASTRUCTURE;

CELIAC DISEASE; CHILD; CHILD, PRESCHOOL; CYTOMEGALOVIRUS INFECTIONS; DIARRHEA, INFANTILE; ENTEROCYTES; HUMANS; INCLUSION BODIES; INFANT; INFANT, NEWBORN; INTESTINAL DISEASES; INTESTINAL MUCOSA; INTESTINE, SMALL; LYMPHANGIECTASIS, INTESTINAL; MICROSCOPY, ELECTRON, TRANSMISSION; MICROVILLI; STEATORRHEA;

EID: 77952245485     PISSN: 01913123     EISSN: 15210758     Source Type: Journal    
DOI: 10.3109/01913121003648410     Document Type: Conference Paper

References (33)

1. Phillips AD. Intractable diarrhoea due to congenital enterocyte defects. Ann Nestlé. 2006;64:15-23.
2. Cuenod B, Brousse N, Goulet O, et al. Clasification of intractable diarrhea in infancy using clinical and immunohistological criteria. Gastroenterology. 1990;99:1037-1043.
3. Bar A, Riskin A, Iancu T, Manov I, Arad A, Shaoul R. A newborn infant with protracted diarrhea and metabolic acidosis. J Pediatr. 2006;150:198-201.
4. Phillips AD, Szafranski M, Man LY, Wall WJ. Periodic acid-Schiff staining abnormality in microvillous atrophy: photometric and ultrastructural studies. J Pediatr Gastroenterol Nutr. 2000;30:34-42.
5. Groisman MM, Amar M, Livne E. CD10: a valuable tool for the light microscopic diagnosis of microvillous inclusion disease (familial microvillous atrophy). Am J Surg Pathol. 2002;26:902-907.
6. Davidson GP, Cutz E, Hamilton MD,Gall DG. Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypolastic villous atrophy. Gastroenterology. 1978;75:783-790.
7. Cutz E, Rhoads JM, Drumm B, Sherman PM, Durie PR, Forstner GG. Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation. N Engl J Med. 1989;320:646-651.
8. Mierau GW, Wills EJ, Wyatt-Ashmead J, Hoffenberg EJ, Cutz E. Microvillous inclusion disease: report of a case with atypical features. Ultrastruct Pathol. 2001;25:517-521.
9. Iancu TC, Mahajnah M, Manov I. Microvillous inclusion disease: ultrastructural variability. Ultrastruct Pathol. 2007;31:173-188.
10. Erickson RP, Larson-Thomé K, Valenzuela RK, Whitaker SE, Shub MD. Navajo microvillous inclusion disease is due to a mutation in MYO5B. Am J Med Genet A. 2008;15:146A:3117-3119.
11. Müller T, Hess MW, Schiefermeier N, et al. MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity Nat Genet. 2008;40:1163-1165.
12. Raafat F, Green NJ, Nathavintharana KA, Booth IW. Intestinal microvillous dystrophy: a variant of microvillous inclusion disease or a new entity? Hum Pathol. 1994;25:1243-1248
13. Refine RM, Cuts E, Griffiths AM, Nag BY, Sherman PM. Tufting naturopathy: a newly recognized clinic pathological entity associated with refractory diarrhea in infants. J Pediatr Gastroenterol Nutr. 1994;18:379-385.
14. Goblet O, Salomon J, Rumple F, Patey-Mariaud de Serres N, Brousse N. Intestinal epithelial dysplasia (tufting enteropathy). Orphanet J Rare Dis. 2007;20:1-6.
15. Eklund EA, Liangwu S, Westphal V, Northrop JL, Freeze HH, Scagua FJ. Congenital disorder of glycosylation (CDG)-Ih patient with a severe hepatogastrointestinal phenotype and evolving central nervous system pathology. J Pediatr. 2005;147:847-850.
16. Mandato C, Brive L, Miura Y, et al. Cryptogenic liver disease in four children: a novel congenital disorder of glycosylation. Pediatr Res. 2006;59:293-298.
17. Collins AE, Ferriero DM. The expanding spectrum of congenital disorders of glycosylation. J Pediatr. 2005;147:728-730.
18. Iancu TC, Mahajnah M, Manov I. The liver in congenital disorders of glycosylation: ultrastructural features. Ultrastruct Pathol. 2007;31:189-197.
19. Wisse E, van't Noordende JM, van der Meulen J, Daems W Th. The pit cell: description of a new type of cell occurring in rat liver sinusoids and peripheral blood. Cell Tissue Res. 1976;173:423-425.
20. Green PHR, Christophe Cellier C. Celiac disease. N Engl J Med. 2007;357:1731-1743
21. Iancu TC, Marsh NM. Mucosal pathology in celiac disease: electron microscopy. Front Gastrointest Res. [Basel, Karger], 1892;19:64-84.
22. Niazi NM, Leight R, Crowe P, Marsh MN. Morphometric analysis of small intestinal mucosa. Virchows Arch [Pathol Anat]. 1984;404:49-60.
23. Hayat M, Cairns A, Dixon MF, O'Mahony S. Quantitation of intraepithelial lymphocytes in human duodenum: what is normal? J Clin Pathol. 2002;55:393-394.
24. Hill DJ, Davidson GP, Cameron DS, Barnes GI. The spectrum of cow's milk allergy in childhood. Acta Paediatr Scand. 1979;68:847-852.
25. Iancu T, Elian E. The intestinal microvillus. Acta Paediatr Scand. 1976;65:65-73. Figure 4 reproduced with the publisher's permission (presently Wiley-Interscience).
26. Crossley JR, Elliott RB. A simple method for diagnosing proteinlosing enteropathies. Br Med J. 1977;12(1 [6058]): 428-429.
27. DobbinsWO III. Electron microscopic study of the intestinal mucosa in intestinal lymphangectasia. Gastroenterology. 1966;51:1004-1017.
28. Bujanover Y, Liebman WM, Goodman JR, Thaler MM. Primary intestinal lymphangectasia. Digestion. 1981;21:107-114.
29. Mirkin DL, Mezoff A, Pysher TJ. Intestinal lymphangectasia in a 33-month-old girl. Ann Diagn Paediatr Pathol. 1998;2:31-35.
30. Bronspiegel N, Zelnick N, Rabinowitz H, Iancu TC. Aplasia cutis congenita and intestinal lymphangectasia. AJDC. 1985;139:509-513.
31. Berriot-Varoqueaux N, Aggerbeck LP, Samson-Bouma M-E, Wetterau LR. The role of the microsomal triglygeride transfer protein in abetalipoproteinemia. Annu Rev Nutr. 2000;20:663-697.
32. Dannoura HA, Berriot-Varoqueaux N, Amati P, et al. Anderson's disease: exclusion of apolipoprotein and intracellular lipid transport genes. Arterioscler Thromb Vasc Biol. 1999;19:2494-2508.
33. Boldrini R, Biselli R, Bosman C. Chylomicron retention disease: the role of ultrastructural examination in differential diagnosis. Pathol Res Pract. 2001;197:753-757.