PR06 NECROTISING FASCIITIS OR PYODERMA GANGRENOSUM ? AN INTERESTING CASE

2007 ◽  
Vol 77 (s1) ◽  
pp. A63-A63
Author(s):  
D. Y. W. Luo ◽  
R. Love
Author(s):  
P. Cirotteau ◽  
D. Heron‐Mermin ◽  
S. Dimicoli‐Salazar ◽  
E. Gérard ◽  
H. Leroy ◽  
...  

2021 ◽  
Vol 12 (2) ◽  
pp. 153-155
Author(s):  
Kritika Pandeyy ◽  
Mansak Shishak ◽  
Neeraj Yadav

Pyoderma gangrenosum (PG) is an uncommon entity based on a diagnosis of exclusion. It can manifest itself mimicking various ulcerative cutaneous conditions and nonhealing wounds. With its less known etiology and presentation, there is a danger of mistreatment. Herein, we present an interesting case of pyoderma gangrenosum in a young woman, developing around the area of a lower segment Cesarean scar, but not involving the scar tissue. The PG was not associated with any underlying systemic ailments and responded well to a tapering dose of oral corticosteroids. Prompt diagnosis and initiation of therapy lead to a good response and favorable prognosis. Recognizing the atypical clinical presentations of PG is pertinent. Treatment with immunosuppressive agents and a multidisciplinary approach are recommended.


2019 ◽  
Vol 16 (6) ◽  
pp. 1347-1353 ◽  
Author(s):  
Cenk Demirdover ◽  
Alper Geyik ◽  
Haluk Vayvada

2017 ◽  
Vol 103 (4) ◽  
pp. 615-617 ◽  
Author(s):  
M. Vaysse-Vic ◽  
P.-A. Mathieu ◽  
A. Charissoux ◽  
J.-L. Charissoux ◽  
P.-S. Marcheix

2021 ◽  
Vol 14 (5) ◽  
pp. e237534
Author(s):  
Cheryl Chong ◽  
Prasad Palanisamy ◽  
Eugene Shen-Ann Yeo

Peristomal pyoderma gangrenosum (PPG) is a rare clinical entity, which can masquerade as the more common and lethal necrotising fasciitis. The authors present a case of PPG in a 65-year-old woman who underwent robotic abdominoperineal resection for low rectal carcinoma and returned 8 days postoperation for peristomal skin ulcerations and pain, accompanied by leucocytosis; thus, she was treated as per necrotising fasciitis and underwent surgical debridement. Thereafter, her wound continued to worsen despite conventional wound care with vacuum-assisted closure and demonstrated signs of pathergy. The case was referred to dermatology where a diagnosis of PPG was made. This case report presents a cautionary tale for fellow clinicians, highlights the diagnostic challenge, and presents an updated literature review on diagnosis and management of this unique condition.


2017 ◽  
Vol 45 (1) ◽  
pp. 63-66 ◽  
Author(s):  
Catherine Besner Morin ◽  
Benoit Côté ◽  
Annie Belisle

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