Bromeo Albert John, Suller Armida
Department of Ophthalmology and Visual Sciences, Philippine General Hospital, University of the Philippines, Manila, Philippines.
BMJ Case Rep. 2019 Jul 8;12(7):e230645. doi: 10.1136/bcr-2019-230645.
A 3-year-old woman presented with a large ulcerated lesion involving the left upper eyelid and left earlobe with erythematous, swollen, undermined and advancing borders. Culture of the ulcer showed no growth of organisms. Treatment with empiric intravenous and topical antibiotics showed no improvement. Workup revealed an elevated white blood cell count with elevated neutrophil count, elevated erythrocyte sedimentation rate and C reactive protein and positive antinuclear antibody. A skin biopsy showed a neutrophilic dermatitis with vasculitis. The patient was started on oral prednisone, which resulted in halting of the progression of ulceration and clinically decreased skin inflammation. The skin biopsy and positive response to corticosteroids confirmed the diagnosis of pyoderma gangrenosum. Pyoderma gangrenosum is a rare inflammatory skin condition and rarely presents as lesions of the eyelid. Early initiation of immunosuppressive therapy prevents disfigurement. Eyelid reconstruction in these cases may prove to be difficult.
一名3岁女性患者,左上眼睑和左耳垂下出现一个大的溃疡性病变,边界呈红斑状、肿胀、潜行性且不断进展。溃疡培养未发现微生物生长。经验性静脉和局部使用抗生素治疗无效。检查发现白细胞计数升高,中性粒细胞计数升高,红细胞沉降率和C反应蛋白升高,抗核抗体阳性。皮肤活检显示为伴有血管炎的嗜中性皮炎。患者开始口服泼尼松,这使得溃疡进展停止,临床皮肤炎症减轻。皮肤活检及对皮质类固醇的阳性反应确诊为坏疽性脓皮病。坏疽性脓皮病是一种罕见的炎症性皮肤病,很少表现为眼睑病变。早期开始免疫抑制治疗可防止毁容。这些病例的眼睑重建可能会很困难。