双侧原发性输卵管浆液性乳头状癌——罕见病例

Satish Arakeri
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摘要

双侧原发性输卵管癌是一种非常罕见的情况。其发病率约占所有妇科恶性肿瘤的0.02%。一名40岁的女性患者因下腹疼痛就诊3个月。骨盆超声显示复杂的双侧附件病变,ORADS评分为4-中等风险。血清CA-125升高。临时诊断为双侧输卵管积脓。切除了带有双侧卵巢和输卵管的子宫。因此,在组织病理学上,最终诊断为原发性双侧输卵管浆液性乳头状癌。双侧原发性输卵管癌是一种非常罕见的情况。术中冷冻研究是为了诊断这个实体。诊断双侧输卵管癌需要高度怀疑,因为这是一种非常罕见的病例,通常与输卵管积脓相混淆。
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Bilateral primary papillary serous carcinoma of the fallopian tube – A rare case scenario
Bilateral primary fallopian tube carcinoma is a very rare case scenario. Approximately, its incidence is 0.02% of all the gynecological malignancy. A 40-year-old female patient visited the hospital with complaints of lower abdominal pain for 3 months. Ultrasound of the pelvis shows complex bilateral adnexal lesions with ORADS score 4 – intermediate risk. The serum CA-125 is elevated. The provisional diagnosis of bilateral pyosalpinx was made. The uterus with bilateral ovaries and fallopian tubes was removed. On histopathology, thus, the final diagnosis of primary bilateral papillary serous carcinoma of the fallopian tube was made. Bilateral primary fallopian tube carcinoma is a very rare case scenario. Intraoperative frozen study is to be done to diagnose this entity. The high degree of suspicion is required to diagnose a case of bilateral fallopian tube carcinoma as it is a very rare case scenario and usually confused for pyosalpinx.
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