Stopa Brittany M, Cuoco Joshua A, Adhikari Srijan, Grider Douglas J, Rogers Cara M, Marvin Eric A
Virginia Tech Carilion School of Medicine, Roanoke, VA, United States.
Section of Neurosurgery, Carilion Clinic, Roanoke, VA, United States.
Front Surg. 2022 Apr 25;9:850050. doi: 10.3389/fsurg.2022.850050. eCollection 2022.
Metastasis of ovarian carcinoma to the central nervous system occurs in <2% of cases and classically localizes within the brain parenchyma. Moreover, leptomeningeal spread of these tumors is an exceedingly rare phenomenon. Here, we conduct a systematic review of the current literature on the natural history, treatment options, and proposed pathogenic mechanisms of leptomeningeal carcinomatosis in ovarian carcinoma. We also report a case of a 67-year-old female with stage IV metastatic ovarian serous carcinoma initially confined to the peritoneal cavity with a stable disease burden over the course of three years. Follow-up imaging demonstrated an intracranial lesion, which was resected via craniotomy, and pathology was consistent with the original diagnosis. Three months after surgery, she developed rapidly progressive dizziness, generalized weakness, fatigue, and ataxia. Repeat MRI demonstrated interval development of extensive and diffusely enhancing dural nodularity, numerous avidly enhancing supratentorial and infratentorial lesions, enhancement of the bilateral trigeminal nerves, internal auditory canals, and exit wound from the surgical site into the posterior aspect of the right-sided neck musculature consistent with diffuse leptomeningeal dissemination. The present case highlights that leptomeningeal dissemination of ovarian carcinoma is a potential yet rare consequence following surgical resection of an ovarian parenchymal metastasis. Progressive clinical symptomatology that develops postoperatively in this patient population should prompt urgent workup to rule out leptomeningeal disease and an expedited radiation oncology consultation if identified.
卵巢癌转移至中枢神经系统的情况在不到2%的病例中出现,经典地定位于脑实质内。此外,这些肿瘤的软脑膜播散是一种极其罕见的现象。在此,我们对当前关于卵巢癌软脑膜癌病的自然史、治疗选择及提出的致病机制的文献进行系统综述。我们还报告了一例67岁女性,患有IV期转移性卵巢浆液性癌,最初局限于腹腔,在三年病程中疾病负担稳定。随访影像学显示颅内有一病变,通过开颅手术切除,病理与原诊断一致。术后三个月,她出现快速进展的头晕、全身无力、疲劳和共济失调。重复MRI显示在间隔期出现广泛且弥漫性强化的硬脑膜结节、许多明显强化的幕上和幕下病变、双侧三叉神经、内耳道强化,以及从手术部位至右侧颈部肌肉组织后方的出口处强化,符合弥漫性软脑膜播散。本病例强调,卵巢癌的软脑膜播散是卵巢实质转移瘤手术切除后一种潜在但罕见的后果。该患者群体术后出现的进行性临床症状应促使紧急检查以排除软脑膜疾病,若确诊则应加快放疗科会诊。