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A case of uterine corpus large cell neuroendocrine carcinoma showing prominent myometrial invasion without any macroscopically clear tumor formation

机译:一例子宫体大细胞神经内分泌癌表现为明显的子宫肌层浸润无肉眼可见的明显肿瘤形成

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摘要

Large cell neuroendocrine carcinoma (LCNEC) arising in the uterine corpus is a very rare. Here, we report our experience with a primary LCNEC in the uterine corpus that showed prominent myometrial invasion without exhibiting any macroscopically distinct tumor formation in the uterine cavity. The patient was a 54-year-old woman. She had a past medical history of right breast cancer and was referred to our department with irregular genital bleeding, elevated serum carcinoembryonic antigen in periodic medical examinations and computed tomography (CT) findings of uterine cavity dilation. Endometrial biopsy suggested a poorly differentiated tumor. Although magnetic resonance imaging (MRI) showed hematometra-like findings in the uterine cavity, it did not indicate any clear endometrial lesion. The myometrium was unequally thickened, and the entire muscle layer showed a high signal intensity on diffusion-weighted images. Fluorine-18-deoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) showed strong FDG accumulation in the whole uterus, and on the bottom of the uterus, there was a ring-shaped accumulation mainly in the muscle layer. The postoperative resected specimen did not show any tumor formation in the uterine cavity, whereas the myometrium was hard and thickened, and colored white overall. Histopathological examination revealed prominent myometrial invasion in most layers, cervical stromal invasion and pelvic lymph node metastasis. The diagnosis was a LCNEC of the uterine corpus, at FIGO stage IIIC1 and pT2N1M0. With these patients, we found that functional metabolic images, such as MRI diffusion-weighted images and FDG-PET/CT, were useful in identifying the lesion. Preoperatively, when a poorly differentiated tumor is estimated and characteristic myometrial invasion is suspected, the possibility of LCNEC should be considered.
机译:子宫体中出现的大细胞神经内分泌癌(LCNEC)非常罕见。在这里,我们报告了我们在子宫体中发生原发性LCNEC的经验,该现象显示出明显的子宫肌层浸润,而在子宫腔中未表现出任何宏观上明显的肿瘤形成。该患者是一名54岁的女性。她曾有右乳腺癌的病史,并因不规则的生殖器出血,血清癌胚抗原升高而被转诊到我们的部门,定期进行体格检查和计算机X线摄影术(CT)检查发现子宫腔扩张。子宫内膜活检提示肿瘤低分化。尽管磁共振成像(MRI)显示子宫腔内有血丝状表现,但并未显示任何清晰的子宫内膜病变。子宫肌层不均匀地增厚,并且整个肌肉层在扩散加权图像上显示出高信号强度。氟-18-脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG-PET / CT)显示,FDG在整个子宫中都有很强的积累,在子宫底部,主要是在肌肉层中有环状积累。术后切除的标本在子宫腔中未显示任何肿瘤形成,而子宫肌层坚硬且增厚,整体呈白色。组织病理学检查显示大多数层存在明显的肌层浸润,宫颈基质浸润和盆腔淋巴结转移。诊断为子宫体的LCNEC,处于FIGO的IIIC1期和pT2N1M0期。对于这些患者,我们发现功能性代谢图像(如MRI弥散加权图像和FDG-PET / CT)可用于识别病变。术前,当估计低分化的肿瘤并怀疑特征性肌层浸润时,应考虑LCNEC的可能性。

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