Zheng Jinfeng, Geng Ming, Li Peifeng, Li Yi, Cao Yongcheng
Department of Pathology, General Hospital of Jinan Military Command, Jinan, Shandong Province, China.
Int J Clin Exp Pathol. 2013 Jul 15;6(8):1688-92. Print 2013.
A 48-year-old woman presented with left abdominal pain and fullness. Computed tomography scan revealed a multicystic mass with multifocal mural nodules. Histologic examination showed a mucinous cystic tumor with cystadenoma, borderline malignant cystadenoma and cystadenocarcinoma, which were associated with sarcoma-like mural nodules (SLMNs) and multifocal anaplastic carcinoma. Mural nodules showed a positive reaction for CD56 and vimentin, but were negative for cytokeratin 7 and SMA. She underwent postoperative chemotherapy and is currently under follow-up; no recurrence or metastases were found in the first year of follow-up. Ovarian mucinous cystic tumor with SLMNs and foci of anaplastic carcinoma is extremely rare. To our knowledge, this case reports the most complex neoplastic and reactive components. Our findings shed some light on the pathogenesis of this rather rare carcinoma. We think that the formation of SLMNs may be the result of the reactive proliferation of undifferentiated mesenchymal cells, while the anaplastic carcinoma may be derived from mucinous epithelium. Moreover, because of difficulties encountered in their differential diagnosis, we think that the existence of foci of anaplastic carcinoma along with SLMNs necessitates careful histologic and immunohistochemical analysis of mural nodules for the determination of treatment and prognosis.
一名48岁女性因左上腹疼痛和饱胀感就诊。计算机断层扫描显示一个多房性肿块,伴有多灶性壁结节。组织学检查显示为黏液性囊性肿瘤,包含囊腺瘤、交界性恶性囊腺瘤和囊腺癌,这些与肉瘤样壁结节(SLMNs)和多灶性间变性癌相关。壁结节对CD56和波形蛋白呈阳性反应,但细胞角蛋白7和平滑肌肌动蛋白呈阴性。她接受了术后化疗,目前正在随访中;随访的第一年未发现复发或转移。伴有SLMNs和间变性癌灶的卵巢黏液性囊性肿瘤极为罕见。据我们所知,本病例报告了最复杂的肿瘤性和反应性成分。我们的发现为这种相当罕见的癌症的发病机制提供了一些线索。我们认为SLMNs的形成可能是未分化间充质细胞反应性增殖的结果,而间变性癌可能起源于黏液上皮。此外,由于在鉴别诊断中遇到困难,我们认为伴有SLMNs的间变性癌灶的存在需要对壁结节进行仔细的组织学和免疫组化分析,以确定治疗方案和预后。