Kwon Chang-Il, Lee Gyeong-Won, Kim Chi-Yeon
Department of Dermatology, Gyeongsang National University School of Medicine, Jinju, Korea.
Division of Hematology-Oncology, Department of Internal Medicine, Gyeongsang Institute of Health Science, Gyeongsang National University Hospital, Gyeongsang National University School of Medicine, Jinju, Korea.
Ann Dermatol. 2022 Jun;34(3):212-215. doi: 10.5021/ad.2022.34.3.212. Epub 2022 May 20.
Unlike classic pyoderma gangrenosum (PG), the bullous variant of PG is typically represented by a painful erythematous papule, plaque, and superficial bulla that progress into the ulceration with bullous margin. Generally, bullous PG is most commonly associated with myeloproliferative disorders, such as acute myeloid leukemia (AML). Bullous PG in AML patients rarely occurs, but once it does, it suggests a poor clinical prognosis. Although many cases of classic PG in AML patients have been reported, bullous PG is relatively rare. Therefore, we present a case of bullous PG that developed in a patient with AML and was successfully treated with high-dose systemic steroids.
与经典坏疽性脓皮病(PG)不同,PG的大疱型通常表现为疼痛性红斑丘疹、斑块和浅表大疱,随后发展为具有大疱边缘的溃疡。一般来说,大疱型PG最常与骨髓增殖性疾病相关,如急性髓系白血病(AML)。AML患者中很少发生大疱型PG,但一旦发生,则提示临床预后不良。虽然已有许多AML患者发生经典PG的病例报道,但大疱型PG相对少见。因此,我们报告1例AML患者发生的大疱型PG,并通过大剂量全身性类固醇成功治疗。