模仿腹膜癌肿的腺瘤样肿瘤:病例报告

IF 1.6 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Uiree Jo
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引用次数: 0

摘要

腺瘤(AT)是一种良性病变,常见于男女生殖道。我们介绍了一例 66 岁女性的病例,她的腺瘤具有模仿腹膜癌的不寻常特征。该肿瘤是在超声检查中偶然发现的,随后的影像学检查让人怀疑是卵巢癌伴腹膜癌转移。冰冻标本的病理诊断结果显示为透明细胞癌,患者随后接受了细胞切除手术。在子宫浆膜上发现了一个 8.5 厘米大小的肿块,并延伸至子宫肌层。此外,还在网膜、阑尾和小肠浆膜以及腹膜上发现了多囊结节病变。经过组织学和大量免疫组化检查,最终诊断为腹腔积液。认识到腹膜癌的多种表现形式对于准确诊断和适当治疗至关重要,因为这些肿瘤可累及多个部位并可模仿腹膜癌,从而可能导致恶性肿瘤的误诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adenomatoid Tumor Mimicking Peritoneal Carcinomatosis: A Case Report.

An adenomatoid tumor (AT) is a benign lesion, which is commonly located in the genital tract of both sexes. We present a case of a 66-yr-old woman with the unusual characteristics of an AT mimicking peritoneal carcinomatosis. The tumor was detected incidentally by ultrasound examination, and an ensuing imaging study raised suspicion of ovarian cancer with peritoneal carcinomatosis. From the pathologic diagnosis of frozen specimens, clear cell carcinoma was noted and the patient subsequently underwent cytoreductive surgery. An 8.5-cm-sized mass was observed on the uterine serosa, extending into the myometrium. In addition, multi-cystic nodular lesions were identified in the omentum, appendiceal and small bowel serosa, and the peritoneum. After histologic and extensive immunohistochemical examinations, the final diagnosis was AT. Recognition of the diverse presentations of AT is crucial for accurate diagnosis and appropriate treatment, as these tumors can involve multiple sites and mimic peritoneal carcinomatosis, potentially leading to a misdiagnosis of malignancy.

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来源期刊
CiteScore
3.90
自引率
12.50%
发文量
154
审稿时长
6-12 weeks
期刊介绍: International Journal of Gynecological Pathology is the official journal of the International Society of Gynecological Pathologists (ISGyP), and provides complete and timely coverage of advances in the understanding and management of gynecological disease. Emphasis is placed on investigations in the field of anatomic pathology. Articles devoted to experimental or animal pathology clearly relevant to an understanding of human disease are published, as are pathological and clinicopathological studies and individual case reports that offer new insights.
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