{Reference Type}: Journal Article
{Title}: [Ulcerative colitis diagnosed with facial pyoderma gangrenosum: a case report].
{Author}: Ogata Y;Soeda A;Saura I;Nemoto E;Tange Y;Enami C;Ochi D;Dai Y;Akiyama S;Ikezawa K;
{Journal}: Nihon Shokakibyo Gakkai Zasshi
{Volume}: 121
{Issue}: 6
{Year}: 2024
暂无{DOI}: 10.11405/nisshoshi.121.481
{Abstract}: 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.