坏疽性脓皮病
溃疡性结肠炎
皮肤病科
医学
结肠炎
内科学
疾病
作者
Yudai Ogata,Atsuko Soeda,Isao Saura,Emi Nemoto,Yoshitaka Tange,Chiaki Enami,Daisuke Ochi,Yuichi Dai,Shintaro Akiyama,Kazuto Ikezawa
出处
期刊:PubMed
[National Institutes of Health]
日期:2024-01-01
卷期号:121 (6): 481-488
标识
DOI:10.11405/nisshoshi.121.481
摘要
Pyoderma gangrenosum (PG) is a sterile inflammatory skin condition that is frequently associated with immune-related diseases, including inflammatory bowel disease (IBD). PG causes noninfectious ulcers. Facial PG is uncommon while PG usually occurs on the trunk and lower limbs. Herein, we report a case of a male teenager with fever, pustules, ulcers, and necrosis on both cheeks. He was initially diagnosed with complicated acne with bacterial infection, but the condition progressed to subcutaneous ulcers despite treatment. Biopsy revealed inflammatory lesions in dermal and subcutaneous tissue with neutrophil infiltration, consistent with PG. Although lacking typical IBD symptoms, blood tests revealed anemia and positive fecal occult blood. Sigmoidoscopy revealed inflammation, ulcers, and pseudopolyps in the colon and rectum, thereby diagnosing ulcerative colitis (UC). After treating PG and UC with prednisolone and skin grafts, golimumab was prescribed. The patient is now in remission. Necrotic tissue buildup can complicate closure in PG cases;this emphasizes the need for effective IBD treatment to facilitate procedures such as skin grafts.
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