Acrodermatitis enteropathica, zinc, and the Paneth cell. A case report with family studies

• Published in: Gastroenterology (New York, N.Y. 1943) Vol. 73; no. 3; p. 587
• Main Authors: Bohane, T D, Cutz, E, Hamilton, J R, Gall, D G
• Format: Journal Article
• Language: English
• Published: United States 01-09-1977
• Subjects: Acrodermatitis - drug therapy; Acrodermatitis - enzymology; Acrodermatitis - genetics; Acrodermatitis - metabolism; Acrodermatitis - pathology; Alkaline Phosphatase - blood; Cytoplasmic Granules - ultrastructure; Epithelial Cells; Epithelium - ultrastructure; Female; Humans; Inclusion Bodies - ultrastructure; Infant; Intestines - pathology; Zinc - blood; Zinc - deficiency; Zinc - therapeutic use
• ISSN: 0016-5085
• DOI: 10.1016/S0016-5085(19)32147-X

An infant with acrodermatitis enteropathica was studied before and after starting zinc therapy. Clinical recovery was rapid, and the plasma zinc, serum and mucosal alkaline phosphatase activities returned to normal. Light microscopy of small intestinal biopsies showed normal mucosa. Electron microscopy of the Paneth cells initially revealed abnormal inclusion bodies which disappeared during therapy, suggesting that the abnormality is secondary to zinc deficiency, and not a primary defect. These abnormal inclusions may represent altered secretory granules and a proliferation of lysosomes. We were unable to define the heterozygous state biochemically or histologically.