Subcorneal Pustular Dermatosis Associated with Palmo-Plantar Pustular Psoriasis: Response to Colchicine Therapy

2004 ◽  
Vol 31 (11) ◽  
pp. 946-948 ◽  
Author(s):  
Christina Stefanaki ◽  
George Kontochristopoulos ◽  
Simeon Kedikoglou ◽  
Eutychia Hatziolou ◽  
Niki Zakopoulou
2021 ◽  
pp. 662-666
Author(s):  
Mitra Barahimi ◽  
Scott Lee ◽  
Kindra Clark-Snustad

We report the case of a 51-year-old male with Crohn’s disease (CD) who developed a reproducible pustular rash after ustekinumab (UST) administration. The patient first presented with a pustular rash on his hands, body, extremities, and scalp starting 5 weeks after his initial weight-based UST induction. The rash resolved spontaneously, then recurred 4 weeks after his first subcutaneous maintenance dose of UST 90 mg. Biopsy of the affected area demonstrated subcorneal pustular dermatosis (SPD). UST was discontinued and the rash resolved. Unfortunately, the patient experienced clinical recurrence of CD, and given prior failure of multiple CD medications, UST was restarted with premedication. Two weeks after UST re-induction, the rash recurred, though less severe. Given improvement in CD symptoms, UST was continued and the rash managed with topical corticosteroids. This is the first case of drug-induced SPD associated with UST. One case report has previously described de novo pustular psoriasis associated with UST in a patient with CD and enteropathic arthritis. Notably, SPD and pustular psoriasis can be histologically indistinguishable. The development of a paradoxical psoriasiform rash is thought to be one of the few dose and duration dependent side effects of TNF-antagonist therapy but has not previously been established as a side effect of UST. This case demonstrates a new potential side effect of UST.


2018 ◽  
Vol 21 (1) ◽  
pp. 28-30
Author(s):  
Yu. V Karacheva ◽  
Anastasia Nikolaevna Smykova

A review of the etiology, pathogenesis, clinical manifestations and histological characteristics of a rare skin pathology -- dermatosis of the subcorneal pustular Sneddon-Wilkinson, is presented. The difficulties of differential diagnosis of this disease with pustular psoriasis, dermatitis herpetiformis Duhring, pyoderma and others are shown. A description of the clinical case of subcorneal pustular dermatosis Sneddon-Wilkinson in a man of 54 years is presented.


2019 ◽  
Vol 7 ◽  
pp. 2050313X1985739
Author(s):  
Touraj Khosravi-Hafshejani ◽  
Jan P Dutz

Generalized pustular psoriasis and subcorneal pustular dermatosis are generalized pustular dermatoses that are characterized by the subcorneal accumulation of neutrophils. Careful examination is important in distinguishing these diseases for appropriate management. Patients with acute generalized pustular psoriasis are systemically unwell with discrete pustules as opposed to the chronicity and associated hypopyon lesions in subcorneal pustular dermatosis. Generalized pustular psoriasis lesions demonstrate psoriasiform changes on histology and the increased expression of Th17 cytokines. We describe a middle-aged woman presenting with chronic annular generalized pustular psoriasis, initially mistaken for subcorneal pustular dermatosis due to their clinical and histological semblance. The patient had recurrent skin disease for 6 years despite conventional therapy of oral retinoid, immunosuppressant and biologic therapy. Complete and persistent clearance of her skin lesions was achieved with secukinumab, an interleukin 17A inhibitor.


Sign in / Sign up

Export Citation Format

Share Document