Miyauchi Kyota, Inoue Akihiro, Ono Teruyuki, Suehiro Satoshi, Watanabe Hideaki, Kitazawa Riko, Kunieda Takeharu
Department of Neurosurgery, Ehime University School of Medicine, Toon, Japan.
Division of Diagnostic Pathology, Ehime University Hospital, Toon, Japan.
Surg Neurol Int. 2025 Jun 27;16:265. doi: 10.25259/SNI_330_2025. eCollection 2025.
Epithelioid hemangioendothelioma (EHE) is a rare malignant endothelial tumor of blood and lymph vessels composed of epithelioid cells within a distinctive myxohyaline stroma. Its predilection sites are soft tissues, bone, lung, and liver, and intracranial metastases are extremely rare. We describe a case of EHE in an elderly patient with pineal body metastasis.
An 84-year-old man presented to our hospital with disturbance of consciousness. Neuroimaging showed hydrocephalus and pineal tumor with hemorrhage on computed tomography and gadolinium enhancement on T1-weighted magnetic resonance imaging. Cerebral angiography showed no obvious tumor staining. F-fluorodeoxyglucose (FDG)-positron emission tomography demonstrated accumulations of FDG consistent with the pineal tumor and in the vessel wall and muscle throughout the body. Various tumor markers in the blood and cerebrospinal fluid were negative. Endoscopic biopsy was performed to confirm the diagnosis and to treat the hydrocephalus by endoscopic third ventriculostomy. Histological examination revealed large epithelioid perivascular cells with abundant pale eosinophilic cytoplasm and cytoplasmic vacuolation. Immunohistochemical studies showed positive results for CD34, CD31, cytokeratin AE1/AE3, and calmodulin binding transcription activator 1, and EHE was therefore diagnosed. Because of poor general condition and progressive tumor growth, radiotherapy was administered 7 days after surgery. At 21 days after surgery, endoscopy performed for progressive anemia revealed metastases in the stomach. The lesions continued to grow and the patient died 2 months after surgery.
We present an extremely rare case of EHE presumed metastasis presenting as an isolated pineal region tumor. If a tumor with hemorrhage is found in the pineal body in an elderly patient, EHE should be considered in the differential diagnosis, even if it is a single tumor lesion.
上皮样血管内皮瘤(EHE)是一种罕见的血液和淋巴管恶性内皮肿瘤,由独特的黏液样透明基质内的上皮样细胞组成。其好发部位为软组织、骨、肺和肝脏,颅内转移极为罕见。我们描述了一例老年患者发生松果体转移的EHE病例。
一名84岁男性因意识障碍入住我院。神经影像学检查显示,计算机断层扫描显示脑积水和松果体肿瘤伴出血,T1加权磁共振成像显示钆增强。脑血管造影未显示明显的肿瘤染色。F-氟脱氧葡萄糖(FDG)-正电子发射断层扫描显示FDG在松果体肿瘤以及全身血管壁和肌肉中积聚。血液和脑脊液中的各种肿瘤标志物均为阴性。进行了内镜活检以确诊,并通过内镜下第三脑室造瘘术治疗脑积水。组织学检查显示大的上皮样血管周围细胞,胞质丰富、淡嗜酸性,有胞质空泡形成。免疫组织化学研究显示CD34、CD31、细胞角蛋白AE1/AE3和钙调蛋白结合转录激活因子1呈阳性,因此诊断为EHE。由于全身状况较差且肿瘤进行性生长,术后7天给予放疗。术后21天,因进行性贫血行内镜检查发现胃转移。病变持续生长,患者术后2个月死亡。
我们报告了一例极为罕见的EHE病例,推测为转移瘤,表现为孤立的松果体区肿瘤。如果老年患者的松果体发现有出血性肿瘤,即使是单个肿瘤病灶,鉴别诊断时也应考虑EHE。