Wang Yun, Song Xin, Guo Chao, Ma Yaqi, Li Yali, Li Weiping, Liu Aijun
Department of Pathology, General Hospital of People's Liberation Army, Beijing 100853, China.
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Zhonghua Fu Chan Ke Za Zhi. 2014 Sep;49(9):659-63.
To analyze the clinicopathologic characteristics of atypical polypoid adenomyoma (APA) of endometrium, and investigate the special characteristics of cancerous transformation from APA.
Fourteen cases of APA were collected in General Hospital of People's Liberation Army from January 2007 to March 2013. The clinical data, morphologic features, immunohistochemistry and the related literature were reviewed.
The median age of the 14 patients was 38 years (ranged from 23 to 72 years), only 1 patient was postmenopausal. The most common symptom was irregular vaginal bleeding (4/14), and 4 patients were identified during routine physical examination for infertility. Among 14 cases, 4 cases were diagnosed as well differentiated endometrioid adenocarcinoma originating from APA, and their median age was 35 years (ranged from 28 to 41 years); color Doppler flow imaging (CDFI) of ultrasound showed rich blood flow signal. The tumors with cancerous components were obviously larger than the usual APA (mean diameter: 4.7 versus 1.8 cm). Histologically, irregular and branched glands were embedded in fibromuscular stroma and the glandular epithelium were atypical hyperplasia in varying degrees. While carcinoma developed in the APA, the sieve, solid and papillary structures were noticeable, and necrosis were common.
APA is a rare lesion of the uterus. Although the clinical behavior is benign in most cases, there may be possible for some cases developing carcinomas. If the APA mass is more than 4 cm in diameter, and microscopically demonstrates prominent sieve, solid, papillary structures and necrosis, the diagnosis of carcinoma developed from APA can be made. Thorough analysis should be done before the most proper therapeutic regimen is drawn up.
分析子宫内膜非典型息肉样腺肌瘤(APA)的临床病理特征,探讨APA癌变的特点。
收集2007年1月至2013年3月解放军总医院收治的14例APA病例,复习其临床资料、形态学特征、免疫组化结果及相关文献。
14例患者的中位年龄为38岁(23~72岁),仅1例为绝经后患者。最常见的症状是不规则阴道出血(4/14),4例患者在不孕症常规体检时被发现。14例中,4例被诊断为起源于APA的高分化子宫内膜样腺癌,其中位年龄为35岁(28~41岁);超声彩色多普勒血流成像(CDFI)显示丰富血流信号。伴有癌变成分的肿瘤明显大于普通APA(平均直径:4.7 cm对1.8 cm)。组织学上,不规则且分支的腺体嵌入纤维肌性间质,腺上皮有不同程度的非典型增生。当APA发生癌变时,筛状、实性和乳头状结构明显,坏死常见。
APA是一种罕见的子宫病变。虽然大多数情况下临床行为为良性,但部分病例可能发生癌变。如果APA肿块直径大于4 cm,且显微镜下显示有明显的筛状、实性、乳头状结构及坏死,则可诊断为APA癌变。在制定最恰当的治疗方案前应进行全面分析。