Jha P K, Rana A, Kapoor S, Kher V
Department of Nephrology, Medanta Institute of Kidney and Urology, Haryana, India.
Department of Pathology and Lab Medicine, Medanta - The Medicity, Gurgaon, Haryana, India.
Indian J Nephrol. 2015 Sep-Oct;25(5):297-9. doi: 10.4103/0971-4065.156900.
Pyoderma gangrenosum (PG) is a rare disorder of unknown etiology characterized by multiple cutaneous ulcers with mucopurulent or hemorrhagic exudate. This sterile neutrophilic dermatosis is known to occur in association with malignancy, infection, autoimmune disorders and drugs. Occurrence of PG in a renal transplant recipient, who is already on immunosuppressants, is rare. We hereby report a renal transplant recipient who developed PG 1-month after transplant and responded well to treatment with escalated dose of oral steroid.
坏疽性脓皮病（PG）是一种病因不明的罕见疾病，其特征为出现多个伴有黏液脓性或血性渗出物的皮肤溃疡。这种无菌性嗜中性皮病已知与恶性肿瘤、感染、自身免疫性疾病及药物有关。在已接受免疫抑制剂治疗的肾移植受者中发生PG的情况较为罕见。我们在此报告一名肾移植受者，该患者在移植后1个月发生了PG，对递增剂量的口服类固醇治疗反应良好。
