Grover disease and bullous pemphigoid: a clinicopathological study of six cases

8Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Grover disease (GD) is an idiopathic dermatosis that typically manifests as itchy papules over the trunk in middle-aged men. Bullous pemphigoid (BP) is an autoimmune bullous disease that affects older people. Not only are the two diseases easily distinguishable on clinical grounds, they are also characterized by differences in histopathology, pathogenesis and response to treatment Thus, the co-occurrence of these two conditions in the same patient is usually considered coincidental. In this report, we present a multicentre retrospective analysis of six patients who developed both GD and BP over a short period of time, and in all cases but one, GD preceded BP. We discuss the clinical and histopathological features of these patients, and the suggested mechanisms of the diseases. We conclude that GD might predispose to the development of BP.

Cite

CITATION STYLE

APA

Ellenbogen, E., Geller, S., Azrielant, S., Zeeli, T., Goldberg, I., Schmidt, E., … Sprecher, E. (2019). Grover disease and bullous pemphigoid: a clinicopathological study of six cases. Clinical and Experimental Dermatology, 44(5), 524–527. https://doi.org/10.1111/ced.13789

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free