Case Report
Copyright ©The Author(s) 2015.
World J Gastroenterol. Sep 28, 2015; 21(36): 10461-10467
Published online Sep 28, 2015. doi: 10.3748/wjg.v21.i36.10461
Figure 1
Figure 1 Histopathologic diagnosis of chronic malabsorption syndrome associated with exudative enteropathy as a result of prolonged intestinal primary lymphangectasia and chronic jejunitis of undefined etiology. A: The jejunum showed slight architectural deviations with flat mucosa due to partial villous atrophy; B: T cell lymphatic infiltrates were normal as seen in CD3 staining, which ruled out celiac disease and lymphoma; The amounts of C: Eosinophilic granulocytes; and D: Mast cells were normal, thus excluding mastocytosis and eosinophilic gastroenteritis. The histological sections were prepared with hematoxylin-eosin staining (magnification × 40) and additional immunohistochemistry was performed.
Figure 2
Figure 2 Disease progression. A: Push enteroscopy and high-pressure balloon dilatation of the stenosis were performed; Histology indicated the development of an B: Adenoma; and D: Carcinoma. Thus, 20 years of persistent inflammation led to malignancy according to an enteritis-dysplasia-adenocarcinoma sequence; C: Unaffected crypts showed strong nuclear MLH1 expression, while neoplastic tissue failed to express MLH1. Histological sections A-D were prepared with hematoxylin-eosin staining (magnification × 40) and additional immunohistochemistry was performed.
Figure 3
Figure 3 Postmortem confirmation of brown bowel syndrome associated with multifocal MLH1-positive small bowel adenocarcinoma.