Department of Radiology (Drs. Shah, Menias, Nguyen, and Martinez).
Department of Radiology (Drs. Shah, Menias, Nguyen, and Martinez).
J Minim Invasive Gynecol. 2024 Feb;31(2):155-160. doi: 10.1016/j.jmig.2023.11.012. Epub 2023 Nov 19.
Epithelial ovarian and fallopian cancers are aggressive lesions that rarely metastasize to the central nervous system. Brain metastases usually occur in the setting of known primary disease or widespread metastatic disease. However, in extremely rare cases, an isolated intracranial neoplasm may be the first presentation of fallopian cancer. To the best of our knowledge, only one such case has been reported previously. We present an illustrative case with multimodality imaging and histopathologic correlation of a fallopian tube carcinoma first presenting with altered mental status secondary to an isolated brain metastasis. A 64-year-old female with no pertinent medical history presented with altered mentation. Initial workup identified a 1.6 cm avidly enhancing, solitary brain lesion at the gray-white junction with associated vasogenic edema concerning for either central nervous system lymphoma or metastatic disease. Additional imaging identified a 7.5 × 3 cm left adnexal lesion, initially thought to be a hydrosalpinx with hemorrhage, but magnetic resonance imaging suggested gynecologic malignancy. No lesions elsewhere in the body were identified. Given the lack of locoregional or systemic disease, the intracranial and pelvic lesions were assumed to represent synchronous but distinct processes. The intracranial lesion was biopsied. Preliminary results were suggestive of lymphoma, but further analysis was consistent with high-grade serous carcinoma of müllerian origin. Positron emission tomography/computed tomography was performed to evaluate for other neoplastic lesions, only highlighting the intracranial and pelvic lesions. At this point, a diagnosis of metastatic fallopian cancer was made. The patient was taken for robot-assisted laparoscopy with surgical debulking of the pelvic neoplasm, pathology demonstrating high-grade serous carcinoma of the fallopian tube, matching that of the intracranial lesion. Even though rare, metastatic fallopian cancer should be considered in patients with isolated brain lesions and adnexal lesions, even in the absence of locoregional or systemic disease.
上皮性卵巢癌和输卵管癌是侵袭性病变,很少转移至中枢神经系统。脑转移通常发生在已知原发性疾病或广泛转移疾病的背景下。然而,在极少数情况下,孤立性颅内肿瘤可能是输卵管癌的首发表现。据我们所知,此前仅报道过一例此类病例。我们报告了一例说明性病例,该病例通过多模态成像和组织病理学相关性,展示了一种首次表现为精神状态改变的输卵管癌,继发于孤立性脑转移。一名 64 岁女性,无相关病史,表现为精神状态改变。初步检查发现灰白色交界处有一个 1.6 厘米大小的活性增强、孤立性脑病变,伴有血管源性水肿,考虑中枢神经系统淋巴瘤或转移性疾病。进一步的影像学检查发现左侧附件有一个 7.5×3 厘米的病变,最初认为是伴有出血的输卵管积水,但磁共振成像提示为妇科恶性肿瘤。未在身体其他部位发现病变。由于缺乏局部或全身疾病,颅内和盆腔病变被认为代表同步但不同的过程。颅内病变进行了活检。初步结果提示为淋巴瘤,但进一步分析结果与源自 Müllerian 的高级别浆液性癌一致。进行正电子发射断层扫描/计算机断层扫描以评估其他肿瘤性病变,仅突出显示颅内和盆腔病变。此时,诊断为转移性输卵管癌。患者接受了机器人辅助腹腔镜检查,以进行盆腔肿瘤的减瘤手术,病理显示为输卵管高级别浆液性癌,与颅内病变相匹配。即使罕见,对于孤立性脑病变和附件病变的患者,即使没有局部或全身疾病,也应考虑转移性输卵管癌的可能性。