Clear cell carcinoma of Müllerian origin

Gallardo Navarro Elias, Mancera Steiner Carlos, Francisco García Rodríguez
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Abstract

Clear cell carcinoma is structures of Mullerian origin, they are associated with mutations in TP53 as they are a high-grade neoplasm, however there is no immunophenotypic pattern that guides us if the origin is from the ovary, uterus, endocervix or endometrium. A 71-year-old female patient who underwent surgery for a right parauterine tumor with a pathological report that corresponded to a clear cell tumor. Subsequently, a staging and cytoreductive laparotomy was performed, performing abdominal cavity lavage, salpingo-oophorectomy of the remaining ovary (left), and pelvic and paraortic lymphadenectomy. , omentectomy and biopsies of the parietal peritoneum, all the material was negative for metastatic disease, 18 months later there was a relapse in the vaginal vault, with the presence of an ovoid tumor measuring 10 cm in diameter, treated with colpectomy, with a report of clear cell carcinoma with CK7+ / Napsin A+ / p53+ protein immunophenotype, with a satisfactory disease-free postoperative period.
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缪勒氏清细胞癌
透明细胞癌是一种起源于穆勒瘤的肿瘤,与 TP53 基因突变有关,因为它们是一种高级别肿瘤,但没有免疫表型模式可以指导我们判断其起源于卵巢、子宫、宫颈内口还是子宫内膜。一位 71 岁的女性患者因右侧子宫旁肿瘤接受了手术,病理报告显示为透明细胞瘤。随后,患者接受了分期和细胞切除腹腔手术,进行了腹腔灌洗、剩余卵巢(左侧)输卵管切除术、盆腔和主动脉旁淋巴结切除术。18 个月后,阴道穹隆复发,出现直径 10 厘米的卵圆形肿瘤,行结肠切除术治疗,报告为透明细胞癌,免疫表型为 CK7+ / Napsin A+ / p53+,术后无病生存期令人满意。
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