Garber Sarah T, Khoury Laith, Bell Diana, Schomer Donald F, Janku Filip, McCutcheon Ian E
Department of Neurosurgery, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.
Department of Pathology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.
World Neurosurg. 2016 Nov;95:621.e13-621.e19. doi: 10.1016/j.wneu.2016.07.111. Epub 2016 Aug 10.
Intracranial spread of an adenoid cystic carcinoma (ACC) of the parotid gland is rare, and metastatic ACC to the splenium of the corpus callosum mimicking butterfly glioblastoma (GBM) has not been reported previously. We report a rare case of metastasis to the splenium of the corpus callosum from ACC of the parotid gland.
The tumor occupied the splenium and mimicked the presentation of a butterfly glioma. The patient had undergone parotidectomy 5 years before presentation with this intracranial lesion. On magnetic resonance imaging, the lesion was separate from the pineal gland and displaced the internal cerebral veins downward. Ventricular obstruction and increased cellularity were also suggested, and multiple fluid-filled cystic spaces were observed. The tumor was partially resected, because the extreme lateral boundary could not be visualized. Histological analysis with anti-c-kit antibody showed strong expression of the epithelial component; immunohistochemistry with anti-p63 antibody revealed nests of positive tumor cells, highlighting the myoepithelial component. The tumor also stained positive for anti-Myb antibody.
The treatment for this lesion is surgical debulking followed by radiation therapy; however, the overall prognosis remains grim because of limited chemotherapy options and a propensity for recurrence in both local and distant fashions. When a tumor with adenoid histological features and a "butterfly" phenotype grows in the corpus callosum in a patient with known parotid ACC, both metastasis and adenoid variant GBM should be considered. Careful clinical and radiological correlation is required to diagnose and treat this rare lesion.
腮腺腺样囊性癌(ACC)的颅内扩散较为罕见,此前尚未有转移性ACC至胼胝体压部并酷似蝶形胶质母细胞瘤(GBM)的报道。我们报告一例罕见的腮腺ACC转移至胼胝体压部的病例。
肿瘤占据胼胝体压部,酷似蝶形胶质瘤的表现。该患者在出现此颅内病变5年前已接受腮腺切除术。在磁共振成像上,病变与松果体分离,并使大脑内静脉向下移位。还提示存在脑室梗阻和细胞增多,且观察到多个充满液体的囊腔。由于无法看清最外侧边界,肿瘤进行了部分切除。用抗c-kit抗体进行组织学分析显示上皮成分强烈表达;用抗p63抗体进行免疫组化显示阳性肿瘤细胞巢,突出了肌上皮成分。肿瘤抗Myb抗体染色也呈阳性。
该病变的治疗是手术减瘤,随后进行放射治疗;然而,由于化疗选择有限以及局部和远处复发倾向,总体预后仍然严峻。当已知患有腮腺ACC的患者胼胝体出现具有腺样组织学特征和“蝶形”表型的肿瘤时,应考虑转移瘤和腺样变异型GBM。需要仔细的临床和影像学相关性分析来诊断和治疗这种罕见病变。