Management of Postsurgical Pyoderma Gangrenosum Following Deep Inferior Epigastric Perforator Flap Breast Reconstruction: A Role for a Dermal Regeneration Template

2021 ◽  
Vol 33 (11) ◽  
pp. E67-E74
Author(s):  
Aishu Ramamurthi ◽  
Karri Adamson ◽  
Kai Yang ◽  
James Sanger ◽  
Justin Ling-LeBlanc ◽  
...  

Introduction. Pyoderma gangrenosum (PG) is a relatively uncommon necrotizing and ulcerative cutaneous disorder. It is often associated with a systemic inflammatory disease but may also present following trauma to the skin due to pathergy. Given its rare occurrence and nonspecific histology, PG is primarily a diagnosis of exclusion, which often results in delayed treatment. Very few cases of PG following autologous breast reconstruction have been reported in the literature, particularly in the absence of systemic disease. Case Report. Presented is the case of a 62-year-old female with a history of ductal carcinoma in situ who underwent a left breast mastectomy with immediate deep inferior epigastric perforator flap breast reconstruction complicated by fever and leukocytosis as well as erythema, edema, and bullae involving the mastectomy flaps. Initially, necrotizing soft-tissue infection was suspected, and 2 debridements were performed. A diagnosis of PG was made on postoperative day 7, and the patient responded favorably to high-dose prednisone. Reconstruction was performed with a bilayer wound matrix and delayed skin grafting. Despite significant loss of mastectomy skin flap, the free flap was preserved. Conclusions. Although PG is a rare complication, it should be considered in the differential diagnosis for patients with atypical presentation of infection following breast reconstruction, even in the absence of systemic inflammatory disease. Early diagnosis and multidisciplinary management may prevent unnecessary surgical intervention and enable flap preservation. Furthermore, bilayer wound matrix placement may be useful as an intermediate reconstruction to determine if it is safe to proceed with skin grafting to avoid further pathergy. The findings in this case suggest that final reconstruction may be safely performed sooner than noted in the literature.

2010 ◽  
Vol 26 (07) ◽  
pp. 475-479 ◽  
Author(s):  
Stephanie Caterson ◽  
Theodore Nyame ◽  
Thuy Phung ◽  
Bernard Lee ◽  
Adam Tobias

2020 ◽  
Vol 6 ◽  
pp. 2513826X1989880
Author(s):  
Nicholas Stone ◽  
Victoria E. McKinnon ◽  
Judy Wismer ◽  
Mark H. McRae

Pyoderma gangrenosum (PG) is a rare dermatologic condition manifesting as sterile, rapidly progressing painful skin ulcerations. It is commonly associated with autoimmune disorders such as inflammatory bowel disease. This case report illustrates a severe case of post-surgical pyoderma gangrenosum (PSPG) following bilateral deep inferior epigastric perforator flap breast reconstruction in a 56-year-old Caucasian woman. Factors delaying diagnosis included negative personal/family history of inflammatory disorders and a clinical presentation more suggestive of breast cellulitis. Refractory antibiotic therapy, subsequent ulceration at multiple breast and abdominal incisions, and pathergic response to tissue biopsy supported an eventual clinical diagnosis of PSPG, 12 days postoperatively, despite equivocal histopathologic findings. Initiation of intravenous immunoglobulin, prednisone therapy, local wound care, and avoidance of debridement led to a full resolution by 5 months postoperatively. This study raises awareness for PSPG and highlights the importance of early recognition and urgent dermatology consultation to expedite optimal treatment and minimize subsequent fat necrosis.


2003 ◽  
Vol 30 (3) ◽  
pp. 359-369 ◽  
Author(s):  
James E Craigie ◽  
Robert J Allen ◽  
Frank J DellaCroce ◽  
Scott K Sullivan

2014 ◽  
Vol 41 (1) ◽  
pp. 63 ◽  
Author(s):  
Ritwik Grover ◽  
Jonas A Nelson ◽  
John P Fischer ◽  
Stephen J Kovach ◽  
Joseph M Serletti ◽  
...  

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