scholarly journals Concurrent pyoderma gangrenosum and subcorneal pustular dermatosis in a patient with monoclonal IgA/λ gammopathy

2011 ◽  
Vol 29 (4) ◽  
pp. 134-136 ◽  
Author(s):  
Ya-Wen Hsiao ◽  
Hua-En Lee ◽  
Tseng-Tong Kuo
2020 ◽  
Vol 111 (10) ◽  
pp. 887-889
Author(s):  
M.C. García del Pozo-Martín de Hijas ◽  
J.L. Agudo-Mena ◽  
M.E. Gómez-Sánchez ◽  
E. Escario-Travesedo

2018 ◽  
Vol 6 (7) ◽  
pp. 1271-1274 ◽  
Author(s):  
Maria Ferrillo ◽  
Alessia Villani ◽  
Gabriella Fabbrocini ◽  
Massimo Mascolo ◽  
Matteo Megna ◽  
...  

BACKGROUND: Subcorneal pustular dermatosis, also known as Sneddon-Wilkinson disease, can be classified as one of the neutrophilic dermatoses together with pyoderma gangrenosum. The development of both SPD and PG in the same patient has rarely been reported and may be a strong indicator of IgA dysglobulinemiaCASE REPORT: We report the case of a 34-year-old woman with a 2-year history of relapsing pustular eruptions mainly affecting the abdomen, gluteus region, elbows, and the extremities. Four years after the onset of subcorneal pustular dermatosis (SPD), she developed pyoderma gangrenosum (PG) on her right hand. In literature, the coexistence of SPD and PG in the same patient has already been described. This co-occurrence might indicate a certain predisposition for immune dysregulation.CONCLUSION: Although the two NDs are often associated with systemic diseases, these patients should be followed up for any malignancy because of the strong association between these disorders.


1991 ◽  
Vol 24 (2) ◽  
pp. 325-328 ◽  
Author(s):  
Peter K. Kohl ◽  
Wolfgang Hartschuh ◽  
Wolfgang Tilgen ◽  
Peter J. Frosch

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