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Coincidence of Intra-Abdominal Splenosis in a Patient with Advanced Ovarian Cancer: Case Report and Review of the Literature

机译:腹腔内脾脏患者患有晚期卵巢癌的患者的巧合:案例报告和对文献的审查

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摘要

Splenosis is a rare disease, which is often discovered incidentally years after surgical procedures on the spleen or traumatic splenic lesions. Through injury of the splenic capsule, splenic cells are able to spread and autoimplant in a fashion similar to the process of metastatic cancer. Here we present the case of a 62-year-old female patient with a palpable tumor of the lower abdomen. Her medical history was unremarkable, except for splenectomy after traumatic splenic lesion in her childhood. Clinical examination and diagnostic imaging raised the suspicion of advanced ovarian cancer, which was further substantiated by the typical presentation of adnexal masses and disseminated peritoneal metastases during the following staging laparotomy. Surprisingly, we also found peritoneal implants macroscopically similar to splenic tissue. Microscopic examination of tissue specimens by intrasurgical frozen section confirmed the diagnosis of intra-abdominal splenosis. The patient then underwent cytoreductive surgery with complete resection of all cancer manifestations, sparing the remaining foci of splenosis to avoid further morbidity. This case demonstrates the rare coincidence of intra-abdominal carcinoma and splenosis, which could lead to intraoperative difficulties by misinterpreting benign splenic tissue. Therefore, splenosis should be considered in patients with medical history of splenic lesions and further diagnostic imaging like Tc-99m-tagged heat-damaged RBC scan could be used for presurgical distinguishing between tumor spread in the abdominal cavity and disseminated splenosis. The presented case report should not only raise awareness for the rare disease splenosis, but also emphasize the need to consider the possibility of simultaneous incidence of benign and malignant intra-abdominal lesions, as to our knowledge this is the first published case of simultaneous peritoneal carcinomatosis and splenosis.
机译:脾脏病是一种罕见的疾病,其通常在脾脏或创伤性脾脏病变上的手术手术后偶然发现。通过脾胶囊的损伤,脾细胞能够以类似于转移性癌症的方法的方式传播和自身制胶。在这里,我们展示了一个62岁女性患者,患有下腹部可触及的肿瘤。她的病史是不起眼的,除了在她童年时期的创伤脾脏病变后脾切除术。临床检查和诊断成像提高了晚期卵巢癌的怀疑,该癌症进一步证实了在下列分期剖腹术期间的附带群和弥散腹膜转移的典型呈递。令人惊讶的是,我们也发现腹膜植入物宏观类似于脾组织。通过胶外冻结部分对组织标本的显微镜检查证实了腹部内脾脏病的诊断。患者随后接受了细胞导致手术,完全切除了所有癌症表现,抑制了脾脏病剩余的焦点,以避免进一步的发病率。本例证明腹部癌细胞和脾脏的罕见吻合,这可能导致误解良性脾组织的术中困难。因此,应考虑脾脏病史的脾脏病史和进一步诊断成像,如TC-99M标记的热损伤RBC扫描等患者可用于肿瘤在腹腔中的肿瘤蔓延和散发脾脏中的诊断成像。本案报告不仅应提高对罕见疾病脾脏病的意识,还要强调需要考虑同时发病良性和腹腔内病变的可能性,至于我们的知识,这是第一个出版的同时腹膜癌案例和脾脏病。

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