Primary melanoma of the bladder: a case report and review of the literature

被引:3
|
作者
Quaquarini, E. [1 ]
Saltalamacchia, G. [1 ,2 ]
Tresoldi, M. M. [3 ]
Schmid, M. [4 ]
Villani, L. [5 ]
Bernardo, A. [1 ]
Guarneri, C. [6 ]
Camerota, T. C. [7 ]
机构
[1] ICS Maugeri IRCCS SpA SB, Med Oncol Unit, Pavia, Italy
[2] Univ Pavia, Dept Internal Med & Therapeut, Pavia, Italy
[3] ICS Maugeri IRCCS SpA SB, Dept Surg, Pavia, Italy
[4] ICS Maugeri IRCCS SpA SB, Visual Rehabil Unit, Pavia, Italy
[5] ICS Maugeri IRCCS SpA SB, Pathol Unit, Pavia, Italy
[6] Univ Messina, Dept Biomed & Dent Sci & Morpho Funct Imaging, Sect Dermatol, Messina, Italy
[7] ICS Maugeri IRCCS SpA SB, Urol, Pavia, Italy
关键词
Bladder cancer; KRAS mutation; Melanoma; Molecular status; Prognosis; PRIMARY MALIGNANT-MELANOMA; MUCOSAL MELANOMAS; CELL MELANOMA;
D O I
10.26355/eurrev_202108_26523
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: Primary bladder melanomas are rare and aggressive neoplasms. We herein described a new case and performed a review of the literature. PATIENTS AND METHODS: We present the case of a 81-year-old woman with a primary mucosal melanoma of the bladder after a history of acral melanoma (KRAS mutated) and lentigo maligna of the forehead. Using PubMed, we found that in literature 38 cases were described. RESULTS: In our patients, during a transurethral resection (TURBT), two bladder lesions were detected. The histologic exam revealed a malignant melanoma, Mib1/ki67: 10-12%, PDL1 <1%. No BRAF, NRAS or KRAS mutations were detected. She subsequently underwent a transurethral revision of the trigone and a partial cystectomy of the dome with bilateral pelvic lymph node dissection. Microscopical findings showed a residual 5 mm non-muscle-invasive melanoma of the bladder, with negativity of the surgical margins and of the 17 pelvic lymph nodes. No adjuvant treatment was proposed. To date the patient is disease-free. CONCLUSIONS: Primary bladder melanoma carries a poor prognosis and poses a therapeutic challenge to clinicians who manage patients with this rare condition. In our experience the multidisciplinary approach for the diagnosis and management of this rare cancer is mandatory.
引用
收藏
页码:5122 / 5128
页数:7
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