Microvillous Inclusion Disease with Abundant Vermiform, Electron-Lucent Vesicles

Ultrastructural Pathology

Volumn 27, Issue 5, 2003, Pages 337-340

  Weeks, Douglas A ^a   Zuppan, Craig W ^b   Malott, Richelle L ^a   Mierau, Gary W ^b,c  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b LOMA LINDA UNIVERSITY   (United States)

^c CHILDREN S HOSPITAL   (United States)

Author keywords

Congenital secretory diarrhea; Electron microscopy; Microvillous inclusion disease

Indexed keywords

ARTICLE; CASE REPORT; CELL ULTRASTRUCTURE; CLINICAL FEATURE; CYTOPLASM; DIARRHEA; DUODENUM BIOPSY; ELECTRON MICROSCOPY; ENTEROPATHY; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INFANT; INTESTINE CELL; MICROVILLOUS INCLUSION DISEASE; PRIORITY JOURNAL;

EID: 0242407566     PISSN: 01913123     EISSN: None     Source Type: Journal    
DOI: 10.1080/01913120390239953     Document Type: Article

References (4)

1. Mierau GW, Wills EJ, Wyatt-Ashmead J, Hoffenberg EJ, Cutz E. Microvillous inclusion disease: report of a case with atypical features. Ultrastruct Pathol. 2001;25:275-279.
2. Phillips AD, Schmitz J. Familial microvillous atrophy: a clinicopathological survey of 23 cases. J Pediatr Gastroenterol Nutr. 1992;14:380-396.
3. Phillips AD, Szafranski M, Man L-Y, Wall WJ. Periodic acid-Schiff staining abnormality in microvillous atrophy: photometric and ultrastructural studies. J Pediatr Gastroenterol Nutr. 2000; 30:34-42.
4. Raafat F, Green NJ, Nathavitharana KA, Booth IW. Intestinal microvillous dystrophy: a variant of microvillous inclusion disease or a new entity? Hum Pathol. 1994;25:1243-1248.