Department of Dermatology and Venereology, All India Institute of Medical Sciences, New Delhi, India.
Department of Dermatology and Venereology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.
Indian J Dermatol Venereol Leprol. 2017 Nov-Dec;83(6):667-672. doi: 10.4103/ijdvl.IJDVL_625_16.
Cyclophosphamide therapy is associated with several urological complications including urinary bladder malignancy. Data on urologic complications of chronic cyclophosphamide therapy for dermatologic conditions is not available.
To study the urocytological profile of pemphigus patients on long-term cyclophosphamide therapy.
In a cross-sectional study, consecutive patients who had received cyclophosphamide therapy for pemphigus for more than 12 months were included. All patients were subjected to urinalysis including microscopy, culture, and urine cytology. Immunocytochemical staining for cytokeratin 20 (CK-20) on urine sediments and ELISA (enzyme-linked immunosorbent assay) for nuclear membrane protein-22 (NMP-22) were performed in all cases. In patients with urinary symptoms, microscopic hematuria, or those detected with abnormal urine sediment cytology, NMP-22, and CK-20 positivity, cystoscopy, and other relevant investigations were also done.
A total of 44 patients (43 of pemphigus vulgaris and one of pemphigus foliaceus) were recruited. Mean duration of cyclophosphamide intake was 2.9 ± 1.7 years (range 1-8 years) with a mean cumulative dose of 53 ± 28.4 g (range 6.5-141 g). Twenty-one cases (47.7%) each were asymptomatic and symptomatic with episodic urinary symptoms [of which two had urinary tract infection (UTI)] and two patients had gross hematuria. Urine cytology revealed mild urothelial nucleomegaly with hyperchromasia in four patients. However, CK-20 and NMP-22 were negative in all samples. Cystoscopy was performed in 21 cases and did not reveal any sign of bladder malignancy.
A relatively small sample size and lack of long-term follow-up were limitations.
In our study, no serious urologic complications were found in pemphigus cases on chronic cyclophosphamide therapy.
环磷酰胺治疗与多种泌尿系统并发症相关,包括膀胱癌。关于皮肤科疾病慢性环磷酰胺治疗的泌尿系统并发症的数据尚不清楚。
研究长期接受环磷酰胺治疗的天疱疮患者的尿细胞学特征。
在一项横断面研究中,纳入了接受环磷酰胺治疗天疱疮超过 12 个月的连续患者。所有患者均接受尿分析,包括显微镜检查、培养和尿细胞学检查。对所有病例进行尿液沉淀物细胞角蛋白 20(CK-20)免疫细胞化学染色和核膜蛋白-22(NMP-22)酶联免疫吸附试验(ELISA)。在有尿路症状、镜下血尿或尿液沉淀物细胞学异常、NMP-22 和 CK-20 阳性的患者中,还进行了膀胱镜检查和其他相关检查。
共纳入 44 例患者(43 例寻常型天疱疮,1 例落叶型天疱疮)。环磷酰胺摄入的平均时间为 2.9±1.7 年(范围 1-8 年),累积剂量平均为 53±28.4g(范围 6.5-141g)。无症状和有症状的患者各 21 例(47.7%),其中有 2 例有间歇性尿路症状(其中 2 例有尿路感染(UTI)),2 例有肉眼血尿。尿液细胞学检查显示 4 例患者轻度尿路上皮核增大伴嗜碱性。然而,所有样本的 CK-20 和 NMP-22 均为阴性。对 21 例患者进行了膀胱镜检查,未发现膀胱恶性肿瘤的迹象。
样本量较小且缺乏长期随访是研究的局限性。
在我们的研究中,慢性环磷酰胺治疗的天疱疮患者未发现严重的泌尿系统并发症。