Clinical Experience of Pyoderma Gangrenosum with Extensive Soft Tissue Necrosis.
- Author:
Sung Yoon LIM
1
;
Dong Ha PARK
;
Nam Suk PAE
;
Myong Chul PARK
Author Information
1. Department of Plastic and Reconstructive Surgery, School of Medicine, Ajou University, Suwon, Korea. mpark@ajou.ac.kr
- Publication Type:Case Report
- Keywords:
Pyoderma gangrenosum;
Necrotizing fasciitis;
Deep ulceration
- MeSH:
Adult;
Debridement;
Dexamethasone;
Drainage;
Fasciitis, Necrotizing;
Fever;
Humans;
Lower Extremity;
Male;
Mass Screening;
Mucous Membrane;
Necrosis;
Negotiating;
Physical Examination;
Polyenes;
Pyoderma;
Pyoderma Gangrenosum;
Skin;
Skin Transplantation;
Transplants;
Ulcer
- From:Journal of the Korean Society of Plastic and Reconstructive Surgeons
2008;35(5):615-618
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Pyoderma gangrenosum is a rare cutaneous ulcerative disease. First described in 1930, the condition is characterized by progressive ulceration with deeply undermined purple-red edge.(1) The lower extremities are most commonly affected but other parts of the skin and mucous membranes may also be involved. Although medical treatments with topical wound therapy are commonly used, surgical intervention is still controversial. In this paper, we report an atypical case of pyoderma gangrenosum which was characterized by extensive soft tissue breakdown. METHODS: A 27-year-old male patient was referred to our institution with a 7 x 8 cm sized deeply undermined ulceration with pus-like discharge and fever. Incision and drainage was performed at another clinic 3 days prior to admission to our institution. After a thorough physical examination and the MRI review, a diagnosis of necrotizing faciitis was made. Accordingly, fasciotomy and debridement was performed. However, the wound enlarged progressively and the patient remained highly febrile for 9 days after the treatment. Septic screening did not reveal any occult infection. After a secondary review of the case, the initial diagnosis of necrotizing fasciitis was rejected and changed to pyoderma gangrenosum. With the use of dexamethasone intravenously, the wound improved dramatically and the fever was eliminated. Steroid mediation was tapered with duration of 1 month. The wound was stabilized and subsequently covered with split-thickness skin graft. RESULTS: Split-thickness skin grafting with 1:1.5 mesh was successfully taken. CONCLUSION: Initial clinical features of pyoderma gangrenosum are very similar to that of necrotizing fasciitis. High fever and progressive ulceration with severe pain could invite earlier surgical approach. The advancing wound margins (the well defined violaceous, undermined border and necrotic ulcer base) and lack of isolation of pathogenic organism was used to make the correct diagnosis of pyoderma gangrenosum. We achieved a good result with proper medication and split-thickness skin graft.
