Abstract

Collagenous sprue (CS) is a distinct clinicopathological disorder histologically defined by a thickened subepithelial band (Freeman, 2011). It is a rare condition which has been recently observed in a significant proportion of sprue-like enteropathy associated with olmesartan, a novel entity described by Rubio-Tapia et al. in 2012. CS is historically associated with a poor prognosis (Marthey et al., 2014). However, histological and clinical improvements have been described in most studies with concomitant usage of corticosteroids and/or gluten-free diet (Marthey et al., 2014). We report a unique case of olmesartan-induced collagenous sprue in a 79-year-old man that showed complete histological and clinical remission with the sole withdrawal of the incriminating drug. The literature on this topic is briefly reviewed.

Highlights

  • Claudine Desruisseaux,1 Michaël Bensoussan,1 Etienne Désilets,1 Hanh-Khiem Tran,1 Robert Arcand,2 Germain Poirier,3 Andrew Wisniewski,1 and Thibaut Manière1

  • We report a unique case of olmesartan-induced collagenous sprue in a 79-year-old man that showed complete histological and clinical remission with the sole withdrawal of the incriminating drug

  • Collagenous sprue (CS) is a rare form of enteropathy that has been classically regarded as a complication of refractory celiac disease, an association that remains controversial [1]

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Summary

Introduction

Claudine Desruisseaux,1 Michaël Bensoussan,1 Etienne Désilets,1 Hanh-Khiem Tran,1 Robert Arcand,2 Germain Poirier,3 Andrew Wisniewski,1 and Thibaut Manière1. Collagenous sprue (CS) is a distinct clinicopathological disorder histologically defined by a thickened subepithelial band (Freeman, 2011). It is a rare condition which has been recently observed in a significant proportion of sprue-like enteropathy associated with olmesartan, a novel entity described by Rubio-Tapia et al in 2012.

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