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首页> 外文期刊>American Journal of Medical Case Reports >Primary Peritoneal Carcinoma: A Case Report of Primary Peritoneal Papilary Serous Adenocarcinoma in a 59 Year Old Postmenopausal Woman
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Primary Peritoneal Carcinoma: A Case Report of Primary Peritoneal Papilary Serous Adenocarcinoma in a 59 Year Old Postmenopausal Woman

机译:原发性腹膜癌:一名59岁绝经后妇女原发性腹膜乳头浆液性腺癌的病例报告

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Primary peritoneal carcinoma is rare and may present with symptoms similar to epithelial ovarian carcinoma which has some histological similarities. This is a case report of a 59 year old woman Para 2 who presented with massive ascites, abdominal pain, difficulty in breathing, abdominal mass and weight loss of three months duration. No conclusive diagnosis could be made after an ultrasound scan and CT-scan investigations showed the ovaries were of normal size but serum CA125 level was markedly elevated. No organ including the ovaries was identified as primary source of the tumour at an initial laparatomy. Specimens were however taken from multiple areas including the peritoneum and the omentum for histopathology. Reports of cytology and histology specimens indicated papillary serous adenocarcinoma with likely primary source being the ovary. Two cycles of neo-adjuvant chemotherapy was administered followed by re-laparatomy where total abdominal hysterectomy plus bilateral salpingoophorectomy, omectomy and surgical reduction of tumour seedlings. Final histopathology ruled out papillary serous adenocarcinoma of the ovary which has similar histological features with papillary serous adenocarcinoma of the peritoneum. Four cycles of adjuvant platinum plus paclitaxel based chemotherapy was then administered and serum CA 125 declined from 214u/ml to 49.5u/ml with no clinical signs of residual disease on completion of chemotherapy. The patient is now on followed-up. Conclusion: Primary peritoneal carcinoma though rare, should be suspected if the peritoneum is involved in a malignancy of an unknown primary source. Management of primary peritoneal carcinoma should involve surgical debulking and appropriate chemotherapy as in ovarian carcinoma.
机译:原发性腹膜癌很少见,可能出现类似于上皮性卵巢癌的症状,并具有一些组织学相似性。这是一例59岁女性Para 2的病例报告,该妇女出现大量腹水,腹痛,呼吸困难,腹部肿块和三个月的体重减轻。超声波扫描和CT扫描显示卵巢大小正常,但血清CA125水平明显升高后,无法做出确凿的诊断。在最初的剖腹手术中,没有包括卵巢在内的器官被确定为肿瘤的主要来源。但是,标本取自多个区域,包括腹膜和网膜,以进行组织病理学检查。细胞学和组织学标本的报告表明乳头状浆液性腺癌可能是卵巢的主要来源。进行了两个周期的新辅助化疗,然后进行再次剖腹手术,其中全腹子宫切除术加双侧输卵管切除术,子宫全切术和手术切除肿瘤苗。最终的组织病理学排除了卵巢的乳头状浆液性腺癌,其组织学特征与腹膜的乳头状浆液性腺癌相似。然后进行四轮辅助性铂加紫杉醇辅助化疗,血清CA 125从214u / ml降至49.5u / ml,完成化疗后无残留疾病的临床征象。该患者正在接受随访。结论:原发性腹膜癌虽然很少见,但如果腹膜参与了未知的原发性恶性肿瘤,则应予以怀疑。如在卵巢癌中一样,原发性腹膜癌的治疗应包括手术切除和适当的化疗。

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