尿细胞学诊断的老年妇女原发性尿道恶性黑色素瘤

K. Niwa, T. Ishihara, S. Mori, Keigo Kuwabara, S. Murase, M. Takenaka, Y. Yamaguchi, Takuji Tanaka
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引用次数: 0

摘要

原发性尿道恶性黑色素瘤是一种极为罕见的恶性肿瘤,早期转移,常延误诊断,预后差。关于这个实体的文献,特别是关于泌尿细胞学的文献是有限的。我们在此报告一例极其罕见的原发性尿道恶性黑色素瘤(MM),发生于一名95岁的日本女性。尿液分析显示巨噬细胞含有棕色颗粒色素,尿细胞学检查显示含有棕色色素的非典型细胞阳性,提示MM。肿瘤活检标本病理检查显示尿道MM。免疫组化结果显示,肿瘤细胞对抗体、HMB-45和Malan-A表现出较强的细胞质反应性。黑色素瘤细胞细胞质和细胞膜c-Kit免疫组化阳性,但未检测到BRAF V600E和N/K-RAS突变。泌尿细胞学和免疫组化检查有助于快速准确诊断尿道MM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Urethral Malignant Melanoma in an Elder Woman Diagnosed by Urine Cytology
Primary urethral malignant melanoma is an extremely rare malignancy with early metastasis and often delayed diagnosis, resulted in poor prognosis. Literature on this entity, especially with regard to urinary cytology is limited. We report here an extremely rare case of primary urethral malignant melanoma (MM) developed in a 95-year-old Japanese woman. A urinalysis showed macrophages containing brown granular pigments, and the urinary cytology was positive for atypical cells containing brown pigments suggestive of MM. Pathological examination of the biopsy specimen from the tumor revealed MM of the urethra. Immunohistochemically, the tumor cells showed strong cytoplasmic reactivities against antibodies, HMB-45 and Malan-A. Melanoma cells were immunohistochemically positive for c-Kit in their cytoplasm and cell membrane, although mutations in BRAF V600E and N/K-RAS were not detected. The urinary cytology and immunohistochemistry were useful for the rapid and accurate diagnosis for the urethral MM.
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