2020
DOI: 10.1080/09273948.2020.1739718
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Characterization and Management of Inflammatory Eye Disease in Patients with Hidradenitis Suppurativa

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Cited by 7 publications
(9 citation statements)
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“…Both her ocular symptoms and signs, and her dermatological condition, improved on immunosuppression, though episodic ocular inflammation did not cease entirely. Previously, remission of inflammatory eye disease associated with HS has been reported with adalimumab treatment, in 40%–50% of treated patients in two case series 6 19…”
Section: Discussionmentioning
confidence: 93%
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“…Both her ocular symptoms and signs, and her dermatological condition, improved on immunosuppression, though episodic ocular inflammation did not cease entirely. Previously, remission of inflammatory eye disease associated with HS has been reported with adalimumab treatment, in 40%–50% of treated patients in two case series 6 19…”
Section: Discussionmentioning
confidence: 93%
“…A common dermatological problem with estimated prevalence of 1%,1 2 hidradenitis suppurativa (HS) has been observed to be associated with inflammatory eye disease, in particular peripheral ulcerative keratitis,3–7 but also interstitial keratitis,8 9 scleritis and uveitis 6 7. In one severe HS case, a middle-aged African American man developed Mooren’s type ulceration, which led to corneal perforation in one eye 5.…”
Section: Introductionmentioning
confidence: 99%
“…Hidradenitis suppurativa is a chronic follicular inflammatory skin disorder characterized by recurrent nodules, sinus tracts, abscesses, and scarring within primarily intertriginous regions. 1 , 2 , 3 Its pathogenesis is believed to be initial occlusion of the folliculopilosebaceous units of apocrine gland-bearing skin that subsequently rupture, prompting both an innate and adaptive immune response to the release of antigens and pro-inflammatory stimuli. 1 , 2 , 3 Coexistence of inflammatory eye disease and HS is rare.…”
Section: Discussionmentioning
confidence: 99%
“… 1 , 2 , 3 Its pathogenesis is believed to be initial occlusion of the folliculopilosebaceous units of apocrine gland-bearing skin that subsequently rupture, prompting both an innate and adaptive immune response to the release of antigens and pro-inflammatory stimuli. 1 , 2 , 3 Coexistence of inflammatory eye disease and HS is rare. In prior studies, the most common manifestation was anterior uveitis, followed by episcleritis/scleritis.…”
Section: Discussionmentioning
confidence: 99%
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