Neutrophilic dermatoses as systemic diseases

Prat, L.; Bouaziz, Jean‐David; Wallach, D.; Vignon‐Pennamen, Marie‐Dominique; Bagot, Martine

doi:10.1016/j.clindermatol.2013.11.004

Cited by 88 publications

(76 citation statements)

References 125 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…Other reported extracutaneous involvement includes amicrobial lymph node suppuration with an aseptic splenic abscess, aseptic leukocyte infiltration of the lung, and hepatic parenchymal infiltration [15]. Internal organ involvement suggests SPD is an inflammatory response to internal disease.…”

Section: Inflammatory and Connective Tissue Diseasesmentioning

confidence: 98%

“…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].…”

Section: Infectionsmentioning

confidence: 98%

“…Usually, SPD is localized to the skin, with mild pruritus and irritation and without constitutional symptoms [13,14]. However, cases presenting with systemic symptoms-such as malaise, fever, arthralgias, abnormalities of hepatic enzymes, aseptic neutrophilic abscesses, or sclerosing glomerulonephritis-have been reported [10,14,15]. See Fig.…”

Section: Clinical Presentationmentioning

confidence: 98%

“…These include connective tissue diseases, inflammatory bowel disease, hypothyroidism, hyperthyroidism, SAPHO (synovitis, acne, pustulosis, hyperostosis, osteitis) syndrome, and multiple sclerosis [5,14,15,[23][24][25][26].…”

Section: Inflammatory and Connective Tissue Diseasesmentioning

confidence: 99%

See 3 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: Inflammatory and Connective Tissue Diseasesmentioning

confidence: 98%

Section: Infectionsmentioning

confidence: 98%

Section: Clinical Presentationmentioning

confidence: 98%

Section: Inflammatory and Connective Tissue Diseasesmentioning

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

show abstract

“…Th e bullous form of SS tends to present with fl accid hemorrhagic bullae that may have undermining, purpuric borders simulating early PG. When it appears localized to the dorsum hands, this form is more commonly associated with underlying malignancy (5). In addition, our patient suff ered from debilitating RA, and although SS is associated with RA, RND is much more strongly associated with severe RA (6,7).…”

Section: Discussionmentioning

confidence: 90%

Acral Vesicles and Bullae in a Patient with Severe Rheumatoid Arthritis

Soza

Griffin

2015

Baylor University Medical Center Proceedings

View full text Add to dashboard Cite

The Skin and Disorders of the Musculoskeletal System

Lovell

2016

Rook's Textbook of Dermatology, Ninth Edition

View full text Add to dashboard Cite

Rheumatological conditions such as tophaceous gout may present initially to the dermatologist; combined clinics with rheumatology are of great value. In addition to autoimmune connective diseases such as systemic lupus and dermatomyositis, several infections and inflammatory conditions present with both skin and joint involvement. Several antirheumatic therapies are associated with cutaneous adverse effects.

show abstract

Neutrophilic dermatoses as systemic diseases

Cited by 88 publications

References 125 publications

Subcorneal Pustular Dermatosis: A Review of 30 Years of Progress

Subcorneal Pustular Dermatosis: A Review of 30 Years of Progress

Acral Vesicles and Bullae in a Patient with Severe Rheumatoid Arthritis

The Skin and Disorders of the Musculoskeletal System

Contact Info

Product

Resources

About