Shakuntala P N, Uma Devi K, Shobha K, Bafna U D, Geetashree M
Department of Gynaecologic Oncology, Kidwai Memorial Institute of Oncology, Dr. M. H. Mari Gowda Road, Bengaluru 560029, India.
Case Rep Oncol Med. 2012;2012:120727. doi: 10.1155/2012/120727. Epub 2012 Dec 6.
Large cell neuroendocrine carcinoma (LCNEC) of the ovary is a rare tumor and is now included in the World Health Organization tumor classification. Its prognosis is generally very poor even when the diagnosis is made at an early stage. We report a case of pure large cell neuroendocrine tumour of ovary, appearing 9 months following laparoscopic type I hysterectomy, bilateral pelvic lymph node dissection with ovarian preservation of anatomically normal looking ovaries performed for a cervical biopsy diagnosis of cervical intraepithelial neoplasia grade III with foci of invasion. The rarity lies in the rapid onset (9 months) of a large tumor following conservation of an anatomically normal ovaries. Surgical debulking and five cycles of chemotherapy (Etoposide and Cisplatin) were administered to the woman. She is on followup with no clinical or radiological evidence of disease recurrence for 6 months.
卵巢大细胞神经内分泌癌(LCNEC)是一种罕见肿瘤,现已被纳入世界卫生组织肿瘤分类。即使在早期诊断,其预后通常也很差。我们报告一例卵巢纯大细胞神经内分泌肿瘤病例,该病例出现在腹腔镜I型子宫切除、双侧盆腔淋巴结清扫并保留外观解剖结构正常的卵巢9个月后,此次手术是因宫颈活检诊断为宫颈上皮内瘤变III级伴浸润灶而进行的。罕见之处在于在保留解剖结构正常的卵巢后9个月迅速出现大肿瘤。对该女性患者进行了肿瘤减灭术和五个周期的化疗(依托泊苷和顺铂)。她目前正在接受随访,6个月来无疾病复发的临床或影像学证据。