Subcorneal pustular dermatosis associated with Mycoplasma pneumoniae infection

Lombart, F.; Dhaille, F.; Lok, C.; Dadban, A.

doi:10.1016/j.jaad.2014.02.038

Cited by 18 publications

(19 citation statements)

References 5 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…Cases of urinary tract infections, upper and/or lower respiratory tract infections, and a primary pulmonary coccidioidomycosis have been reported immediately prior to presentation of SPD [15,50]. Reports of Mycoplasma pneumoniae infection of acutely ill patients, confirmed with serology or [48] polymerase chain reaction on throat swabs, had an associated SPD-type cutaneous eruption [15,[51][52][53][54]. Lombart et al [51] suggest including M. pneumoniae in the work-up for SPD, especially with children.…”

Section: Infectionsmentioning

confidence: 99%

“…A third case of seropositive arthritis and SPD was effectively controlled with etanercept alone [28]. A few reports of mild M. pneumoniae upper respiratory infections associated with SPD have responded to oral dapsone without recurrence [51]. One patient discontinued dapsone therapy because of nausea, and the skin lesions were successfully treated with topical corticosteroids alone [51].…”

Section: Treatment Of Spd With Other Disease Associationsmentioning

confidence: 99%

“…A few reports of mild M. pneumoniae upper respiratory infections associated with SPD have responded to oral dapsone without recurrence [51]. One patient discontinued dapsone therapy because of nausea, and the skin lesions were successfully treated with topical corticosteroids alone [51]. Table 4 lists successful treatment reported in literature, with dosages, patient type, and clinical course.…”

Section: Treatment Of Spd With Other Disease Associationsmentioning

confidence: 99%

See 2 more Smart Citations

Subcorneal Pustular Dermatosis: A Review of 30 Years of Progress

2016

View full text Add to dashboard Cite

Subcorneal pustular dermatosis (SPD), also known as Sneddon-Wilkinson disease, is a rare, benign yet relapsing pustular dermatosis. Its incidence and prevalence have not been well studied. It characteristically presents as hypopyon pustules on the trunk and intertriginous areas of the body. SPD is similar to two other disease entities. Both SPD-type immunoglobulin (Ig)-A pemphigus and annular pustular psoriasis clinically and histologically present similarly to SPD. Immunologic studies separate SPD-type IgA pemphigus from SPD and pustular psoriasis. However, there is still an unclear designation as to whether SPD is its own entity distinct from pustular psoriasis, as the once thought characteristic histologic picture of psoriasis does not hold true for pustular psoriasis. SPD has been reported to occur in association with several neoplastic, immunologic, and inflammatory conditions. Dapsone remains the first-line treatment for SPD, although dapsone-resistant cases have been increasingly reported. Other therapies have been used singly or as adjunctive therapy with success, such as corticosteroids, immunosuppressive agents, tumor necrosis factor inhibitors, and ultraviolet light therapy. This article provides a review of the last 30 years of available literature, with a focus on successful treatment options and a suggestion for reappraisal of the classification of SPD.

show abstract

Section: Infectionsmentioning

confidence: 99%

Section: Treatment Of Spd With Other Disease Associationsmentioning

confidence: 99%

Section: Treatment Of Spd With Other Disease Associationsmentioning

confidence: 99%

See 1 more Smart Citation

Subcorneal Pustular Dermatosis: A Review of 30 Years of Progress

2016

View full text Add to dashboard Cite

show abstract

“…Имеются описания СП в ассоциации с так называемыми IgA моноклональными гаммапатиями [9], множественной миеломой [10] и аутоиммунными заболеваниями, такими как ревматоидный артрит [11] [17], цистозными поражениями печени при некоторых гельминтозах [18], гипертиреозом [19] и тимомой [20].…”

unclassified

“…Содержимое гнойничков считается стерильным, хотя казуистически может быть вторично инфицировано золотистым стафилококком или некоторыми видами стрептококков. В одном из исследований в содержимом пустул была высеяна Micoplasma pneumonie, но, по данным этого же исследования, пациент получал 3-месячное лечение дапсоном и рецидива заболевания зарегистрировано не было, несмотря на отсутствие антибиотикотерапии [17].…”

unclassified

Sneddon — Wilkinson disease: Review of the modern literature

Drozhdina

Кошкин

2019

Vestnik dermatologii i venerologii

View full text Add to dashboard Cite

The article provides a current overview of the correlation between a rare dermatosis — subcorneal pustulosis (Sneddon — Wilkinson disease) — and various diseases of internal organs; features of immunological changes; the role of desmocollin 1, chemoatractants, interleukin-1β, interleukin-6, interleukin-8, interleukin-10, leukotriene B4, tumour necrosis factor-alpha and K5a complement fraction in the pathogenesis of the disease. In this work, the authors describe the features of the clinical picture of the disease, as well as diagnostic criteria, including the use of serum protein electrophoresis. Histological features of the disease are discussed in detail. In addition, modern methods for treating this disease, including the use of dapsone, acitretin, infliximab, PUVA therapy are presented.

show abstract

Multiple Circinate, Sterile, Flaccid, Relapsing Pustules

Kundak

Ergin

2019

Pediatric Autoimmunity and Transplantation

View full text Add to dashboard Cite

Subcorneal pustular dermatosis associated with Mycoplasma pneumoniae infection

Cited by 18 publications

References 5 publications

Subcorneal Pustular Dermatosis: A Review of 30 Years of Progress

Subcorneal Pustular Dermatosis: A Review of 30 Years of Progress

Sneddon — Wilkinson disease: Review of the modern literature

Multiple Circinate, Sterile, Flaccid, Relapsing Pustules

Contact Info

Product

Resources

About