2015
DOI: 10.11604/pamj.2015.21.151.6364
|View full text |Cite
|
Sign up to set email alerts
|

Coexistence of pyoderma gangrenosum and sweet’s syndrome in a patient with ulcerative colitis

Abstract: Pyoderma gangrenosum (PG) and Sweet's Syndrome (SS) are inflammatory skin diseases caused by the accumulation of neutrophils in the skin and, rarely, in internal organs. These neutrophilic dermatosis (NDs) are distinguished by the existence of forms of transition or overlap. They are frequently associated to systemic diseases especially hematologic and gastrointestinal ones. We report a case of a patient with ulcerative colitis (UC) who successively developed two types of NDs: PG then SS. A 66 years old patien… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

1
2
0

Year Published

2018
2018
2023
2023

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 8 publications
(3 citation statements)
references
References 9 publications
1
2
0
Order By: Relevance
“…Some authors believe that PG and Sweet's syndrome represent a continuum of spectrum of disease. [ 7 8 ] Our finding of Sweet's-like lesion also supports this hypothesis. PG and Sweet's syndrome share many features including response to immunosuppressive therapy.…”
supporting
confidence: 83%
“…Some authors believe that PG and Sweet's syndrome represent a continuum of spectrum of disease. [ 7 8 ] Our finding of Sweet's-like lesion also supports this hypothesis. PG and Sweet's syndrome share many features including response to immunosuppressive therapy.…”
supporting
confidence: 83%
“…This review found that Crohn’s disease is the most common reported underlying condition in SS. The association of PG and IBD is well recognized; however, the association of SS and IBD should not be overlooked [14]. Appropriate review of systems and workup should be considered.…”
Section: Discussionmentioning
confidence: 99%
“…Clinical assessment should include timing of disease onset as well as a thorough review of systems to initially evaluate for conditions such as recent infection, malignancy, pregnancy, and autoimmune disease, due to their known associations with ND. Surveillance of the entire skin should be performed as the distribution of lesions of the same disease can vary between patients (e.g., cases of both proximal and distal distributions of neutrophilic eccrine hidradenitis have been described), as well as the overlap between lesions of different NDs have also been reported [ 16 ]. While the appropriate description of eruption morphology is crucial to initial differential diagnoses, clinico-pathologic correlation is essential for diagnosis and is often a major diagnostic criterion for NDs [ 4 ].…”
Section: General Work-upmentioning
confidence: 99%