Baggar Soufiane, Ouahbi Hajar, Azegrar Meryem, El M'rabet Fatima Zahra, Arifi Samia, Mellas Nawfel
Service d'Oncologie Médicale CHU Hassan II, Fès, Maroc.
Pan Afr Med J. 2017 Jun 2;27:82. doi: 10.11604/pamj.2017.27.82.10902. eCollection 2017.
Small cell neuroendocrine carcinomas of the gynecologic tract are unusual, accounting for only 2% of the cervical cancers. Given the rarity of these tumors and the absence of randomized trials, their diagnosis and treatment programmes are difficult and are essentially based on those of neuroendocrine tumors of the lung. As in the case of the neuroendocrine tumors of the lung and despite multimodal treatment they are associated with a poor prognosis. We here report a new case of small cell neuroendocrine carcinoma of the cervix and, throught a literature review, we highlight the various aspects of this rare entity.
妇科小细胞神经内分泌癌较为罕见，仅占宫颈癌的2%。鉴于这些肿瘤的罕见性以及缺乏随机试验，其诊断和治疗方案颇具难度，且基本上是基于肺癌神经内分泌肿瘤的方案。与肺癌神经内分泌肿瘤一样，尽管采用了多模式治疗，它们的预后仍然很差。我们在此报告一例新的宫颈小细胞神经内分泌癌病例，并通过文献综述强调了这一罕见实体的各个方面。
