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RFP Journal of Dermatology

Volume  5, Issue 2, July-December 2020, Pages 55-58
 

Case Report

Pyoderma Gangrenosum and Behcet’s Disease Overlap –A Case Report

Dhruv Patel1, Jinal Tandel2, Pragya A Nair3

13rd Year Resident, 22nd Year Resident, 3Professor and Head, Department of Dermatology, Venereology and Leprosy, Shree Krishna Hospital Pramukhswami Medical College Karamsad, Anand, Gujarat 388325, India.

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Abstract

Pyoderma gangrenosum is a rare, chronic, sterile,pustular and progressive ulcerative disease with 4 clinical and histological variants named as ulcerative, pustular, bullous and vegetative. Behcet’s disease is a complex of multisystem disease characterized by orogenital ulceration and eye disease as a classic triad with involvement of other systems . BD and PG , both are neutrophilic dermatoses with oral and genital ulcerations having different frequency. The clinical features of mucosal ulcers are different to some degree between the two diseases, but there is a histopathological distinction between PG and BD . Association of BD and PG are rare but do occur . We report here a case of BD who subsequently developed genital ulcerative PG.

Keywords: Pyoderma gangrenosum; Behcet’s disease; Neutrophilic dermatosis; Orogenital ulcers.


Corresponding Author : Pragya Nair