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[Pyoderma gangrenosum with lung involvement treated with infliximab]
D Deregnaucourt1, S Buche, S Coopman
1Service de dermatologie, université de Lille-2, hôpital Claude-Huriez, CHRU de Lille, rue Michel-Polonovski, 59037 Lille cedex, France. delphine.deregnaucourt@gmail.com
Pyoderma gangrenosum (PG) is a rare skin condition linked to inflammatory bowel disease. This case highlights successful treatment of severe PG with lung involvement using infliximab when corticosteroids failed.
Area of Science:
- Dermatology
- Pulmonology
- Gastroenterology
Background:
- Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis.
- It is frequently associated with systemic conditions, notably chronic inflammatory bowel diseases (IBD).
- Extracutaneous manifestations are common, with pulmonary involvement being the most frequent.
Observation:
- A case of PG with concurrent skin and lung involvement is presented.
- The patient had severe ulcerative colitis (UC) and was treated with high-dose corticosteroids.
- Lung involvement was identified before initiating anti-TNFα therapy.
Findings:
- Infliximab treatment led to rapid improvement in both pulmonary and cutaneous lesions.
- The patient's condition worsened under corticosteroid therapy, indicating a need for alternative treatment.
- Simultaneous skin and lung lesions suggestive of abscesses warrant suspicion of visceral involvement.
Implications:
- This case underscores the importance of considering visceral involvement in patients with simultaneous cutaneous and pulmonary PG lesions.
- While corticosteroids are a first-line treatment, anti-TNFα therapy, such as infliximab, can be effective in refractory cases or those with significant systemic disease.
- Early diagnosis and appropriate management are crucial for improving outcomes in complex PG cases.
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The first classification is based on the development of the disease, and it includes the following categories:
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