Urology Department, René Dubos Hospital, Pontoise, France.
Nuclear Medicine Department, René Dubos Hospital, Pontoise, France.
J Med Case Rep. 2021 May 7;15(1):254. doi: 10.1186/s13256-021-02830-5.
Primitive neuroendocrine prostate neoplasms are rarely reported. This entity comprises carcinoïd tumors and poorly differentiated neuroendocrine tumors, mainly those of the small-cell type. Large-cell-type primitive tumors are exceptional, and only nine cases are reported in the literature. Similar to neuroendocrine tumors of the prostate, large-cell-type primitive tumors may be observed in the context of conventional adenocarcinoma during androgen deprivation therapy or as prostatic metastasis of a distant neuroendocrine tumor, mainly pulmonary neoplasms.
We report a Caucasian case of a mixed prostatic carcinoma, with the largest component being the large-cell neuroendocine carcinoma, in a patient who underwent a total prostatectomy for a localized cancer. Diagnostic, histological, therapeutic and evolutive aspects are reported and discussed.
Large-cell primitive prostate neuroendocrine carcinoma is a rare but aggressive histological entity, which can be associated or not with an adenocarcinomatous component. Mixed forms have a better outcome, mainly when diagnosed at an early stage.
原始神经内分泌前列腺肿瘤很少见。该实体包括类癌肿瘤和分化不良的神经内分泌肿瘤,主要是小细胞型。大细胞型原始肿瘤较为罕见,文献中仅报道了 9 例。与前列腺的神经内分泌肿瘤类似,大细胞型原始肿瘤可能在雄激素剥夺治疗期间观察到常规腺癌的背景下出现,或作为远处神经内分泌肿瘤的前列腺转移,主要为肺肿瘤。
我们报告了一个白种人病例,为混合性前列腺癌,最大成分为大细胞神经内分泌癌,患者因局限性癌症接受了全前列腺切除术。报告并讨论了诊断、组织学、治疗和演变方面。
大细胞原始前列腺神经内分泌癌是一种罕见但具有侵袭性的组织学实体,可能与腺癌成分相关或不相关。混合形式的预后更好,主要是在早期诊断时。