由腔内支气管源性肿瘤栓子引起的转移性大脑中动脉动脉瘤

C. Randazzo, A. Sharan
{"title":"由腔内支气管源性肿瘤栓子引起的转移性大脑中动脉动脉瘤","authors":"C. Randazzo, A. Sharan","doi":"10.29046/JHNJ.004.3.006","DOIUrl":null,"url":null,"abstract":"Objective and Importance: To describe the clinical presentation and neuropathological findings of metastatic cerebral aneurysms of bronchogenic origin. Metastatic bronchogenic cerebral aneurysms are exceptionally rare and have only been reported in association with high grade hemorrhage. Clinical Presentation: One patient presenting with a history of headache, speech difficulty, left-sided “numbness”, left seventh nerve palsy and left hemiparesis was found to have intraparenchymal and subarachnoid hemorrhage with an aneurysm of the right distal Sylvian middle cerebral artery. Intervention: Pterional craniotomy with excision of mycotic segment. Surgical specimen sent to pathology for routine histology and immunohistochemistry. Conclusion: Patients with metastatic cerebral aneuryms of bronchogenic origin usually present with subarachnoid hemorrhage, contrary to prior observations that “hemorrhage from neoplasia-induced aneurysms is paradoxically rare.” A tumor embolus should be considered in the differential diagnosis of a mycotic aneurysm. Cerebral aneurysms have been reported as a complication of primary extracranial neoplasms. The preponderance of such cases has been associated with cardiac myxomas and choriocarcinomas. Olmsted and McGee5 report approximately a 45% systemic embolization rate, half of which may be cerebral, in patients with left atrial myxoma. Weir et al.7 described mycotic aneurysms from choriocarcinoma as specifically being distal, lobulated, and fusiform. Pullar et al.6 reported a series of eight cases of metastatic cerebral aneurysms secondary to choriocarcinoma. There have only been four reported cases of metastatic cerebral aneurysm of bronchogenic origin1-4 The first case was described in 1982 by Ho2. Ho described a fatal intracerebral hemorrhage associated with an aneurysm in the medial aspect of the occipital lobe. Histologically, the lumen of the vessel contained collections of neoplastic cells that had invaded the vessel wall and destroyed the native cytoarchitecture. Kochi et al.3 described an intracerebral hematoma from rupture of a metastatic cerebral bronchogenic aneurysm in a cortical branch of the left posterior temporal artery. Murata et al.4 reported intracerebral hematoma from rupture of a metastatic cerebral bronchogenic aneurysm from a cortical branch of the posterior cerebral artery. Gliemroth et al.1 reported recurrent and fatal subarachnoid hemorrhage from rupture of a metastatic cerebral bronchogenic aneurysm of the anterior inferior cerebellar artery. This patient also developed a mycotic neoplastic aneurysm in the contralateral anterior inferior cerebellar artery. Previous reports* of metastatic cerebral aneurysms postulated a low rate of hemorrhage. The four cases reported to date of metastatic cerebral bronchogenic aneurysm and our case, representing the fifth, have all presented with high grade subarachnoid hemorrhage. Case Report A 43-year-old female with a history of hypertension, asthma, intravenous drug abuse, hepatitis, a right apical lung nodule and a significant smoking history acutely presented to the Emergency Department complaining of speech difficulty and left sided “numbness.” Review of systems discovered a transient headache one week and one month prior to presentation. Physical examination demonstrated 4 out of 5 strength in the left upper and lower extremity on the left with hyperreflexia and an ipsilateral Babinski sign. * circa 2000 Figure 1 Metastatic cerebral artery aneurysm. Complete cross section of aneurysm entirely occluded by partially necrotic metastatic bronchogenic carcinoma. Immunohistochemical stain for cytokeratin CK7, original magnification 40X. 1 Randazzo et al.: Metastatic MCA Aneurysm Caused by Tumor Embolus Produced by The Berkeley Electronic Press, 2009 14 JHN JOURNAL CT of the head was significant for Grade IV subarachnoid hemorrhage and a small intracerebral hemorrhage. A transfemoral cerebral angiogram revealed a right distal middle cerebral artery aneurysm. No other aneurysms were discovered. Subsequently, the patient underwent a right pterional craniotomy with excision of a right middle cerebral artery aneurysm. The resected portion of the middle cerebral artery sent to the pathology lab was i.dentified as a highly anaplastic intraluminal neoplasm that was likely metastatic in origin. Immunohistochemical staining was strongly positive for cytokeratins AE1, CK7 (Figure 1) and CAM5.2 (Figure 2). Hematoxylin and eosin staining demonstrated tumor embolus with invasion through the internal elastic membrane of the middle cerebral artery (Figure 3). Based on these results and the patient’s known lung nodule, it was concluded that the specimen represented a metastatic carcinoma most likely from the lung. A multi-disciplinary team was assembled to further investigate and treat the patient for a primary lung carcinoma. The final impression of the oncologist was that the patient’s metastatic anaplastic carcinoma was most likely from her lung. The patient underwent whole brain irradiation and thoracic surgery was consulted for an open lung biopsy. Discussion Cerebral aneurysms due to metastatic tumor emboli are quite rare. In Ho’s2 early 1982 report of metastatic cerebral aneurysm of bronchogenic origin, he notes 23 documented cases of non-bronchogenic cerebral metastatic aneurysms. Approximately 70% of these cases were due to cardiac myxomas and 22% from choriocarcinomas. Since the publication of this article there have been three other cases of metastatic lung cancer causing cerebral aneurysms3-5. The currently reported case represents the fifth individual. The small number of cases which have been reported limit our ability to characterize these metastatic aneurysms (Table 1). The documented cases do not demonstrate gender or age as risk factors for the development of these aneurysms. Additionally, the histologic subtype of bronchogenic carcinoma does not appear to favor neoplastic aneurysms, as both squamous and small-cell lung carcinoma have been identified in tumor emboli. It is not evident that a particular artery or location has a greater chance of developing a neoplastic aneurysm. One observation that is clear is that all of the reported cases have been complicated by hemorrhage. It is unclear whether it is an inherent property of the primary carcinoma that results in hemorrhage or if observation bias results in the discovery of these aneurysms only when they bleed. If these aneurysms were often present without bleeding; however, they would most likely be reported in postmortem studies as have emboli from cardiac myxomas and choriocarcinomas. Conclusion The present case represents a rare, yet docu- mented complication of primary bronchogenic carcinoma. Since the first case was described by Ho in 1982, several other cases have been iden- tified. The limited number of cases prohibits identification of clear patterns. The recognition of neoplastic aneurysm formation as a devastat- ing complication of bronchogenic carcinoma is necessary in the differential diagnosis of mycotic aneurysms. References 1. Gliemroth J, Nowak G, Kehler U, Arnold H, Gaebel C: Neoplastic cerebral aneurysm from metastatic lung adeno- carcinoma associated with cerebral thrombosis and recurrent subarachnoid haemorrhage. J Neurol Neurosurg Psychiatry 66: 246-247, 1999. 2. Ho KL: Neoplastic aneurysm and intracranial hemorrhage. Cancer 50: 2935-2940, 1982. 3. Kochi N, Tani E, Yokota M, Nakaya Y: Neoplastic cerebral aneurysm from lung cancer. Case report. J Neurosurg 60: 640-643, 1984. 4. Murata J, Sawamura Y, Takahashi A, Abe H, Saitoh H: Intracerebral hemorrhage caused by a neoplastic aneurysm from small-cell lung carcinoma: case report. Neurosurgery 32: 124-126, 1993. 5. Olmsted WW, McGee TP: The pathogenesis of peripheral aneurysms of the central nervous system: a subject review from the AFIP. Radiology 123: 661-666, 1977. 6. Pullar M, Blumbergs PC, Phillips GE, Carney PG: Neoplastic cerebral aneurysm from metastatic gestational choriocarci- noma. Case report. J Neurosurg 63: 644-647, 1985. 7. Weir B, MacDonald N, Mielke B: Intracranial vascular compli- cations of choriocarcinoma. Neurosurgery 2: 138-142, 1978. Figure 2 Metastatic cerebral artery aneurysm. Tumor embolus adherent to wall of artery. Immunohistochemical stain for cytokeratin CAM5.2, original magnification 200X. Figure 3 Metastatic cerebral artery aneurysm. Tumor embolus with invasion through internal elastic membrane Table 1. Author Demographics Type of Cancer Location Complications Ho (2) 68, male Bronchogenic Right Posterior Hemorrhage, Cerebral A. Rupture Murata et al (4) 63, male Small Cell (lung) Anomalous Hematoma Artery Kochi et al (3) 56, male Undifferentiated Left Posterior Hematoma, Squamous Cell (lung) Temporal A. Rupture Gliemroth et al (1) 38, female Adenocarcinoma Bilateral Anterior Hematoma (lung) Inferior Cerebellar A. Rupture Current study 43, female Bronchogenic Right Middle Hemorrhage Cerebral A. 2 JHN Journal, Vol. 4 [2009], Iss. 3, Art. 6 http://jdc.jefferson.edu/jhnj/vol4/iss3/6","PeriodicalId":355574,"journal":{"name":"JHN Journal","volume":"17 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"A Metastatic Middle Cerebral Artery Aneurysm Caused by an Intraluminal Bronchogenic Tumor Embolus\",\"authors\":\"C. Randazzo, A. Sharan\",\"doi\":\"10.29046/JHNJ.004.3.006\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective and Importance: To describe the clinical presentation and neuropathological findings of metastatic cerebral aneurysms of bronchogenic origin. Metastatic bronchogenic cerebral aneurysms are exceptionally rare and have only been reported in association with high grade hemorrhage. Clinical Presentation: One patient presenting with a history of headache, speech difficulty, left-sided “numbness”, left seventh nerve palsy and left hemiparesis was found to have intraparenchymal and subarachnoid hemorrhage with an aneurysm of the right distal Sylvian middle cerebral artery. Intervention: Pterional craniotomy with excision of mycotic segment. Surgical specimen sent to pathology for routine histology and immunohistochemistry. Conclusion: Patients with metastatic cerebral aneuryms of bronchogenic origin usually present with subarachnoid hemorrhage, contrary to prior observations that “hemorrhage from neoplasia-induced aneurysms is paradoxically rare.” A tumor embolus should be considered in the differential diagnosis of a mycotic aneurysm. Cerebral aneurysms have been reported as a complication of primary extracranial neoplasms. The preponderance of such cases has been associated with cardiac myxomas and choriocarcinomas. Olmsted and McGee5 report approximately a 45% systemic embolization rate, half of which may be cerebral, in patients with left atrial myxoma. Weir et al.7 described mycotic aneurysms from choriocarcinoma as specifically being distal, lobulated, and fusiform. Pullar et al.6 reported a series of eight cases of metastatic cerebral aneurysms secondary to choriocarcinoma. There have only been four reported cases of metastatic cerebral aneurysm of bronchogenic origin1-4 The first case was described in 1982 by Ho2. Ho described a fatal intracerebral hemorrhage associated with an aneurysm in the medial aspect of the occipital lobe. Histologically, the lumen of the vessel contained collections of neoplastic cells that had invaded the vessel wall and destroyed the native cytoarchitecture. Kochi et al.3 described an intracerebral hematoma from rupture of a metastatic cerebral bronchogenic aneurysm in a cortical branch of the left posterior temporal artery. Murata et al.4 reported intracerebral hematoma from rupture of a metastatic cerebral bronchogenic aneurysm from a cortical branch of the posterior cerebral artery. Gliemroth et al.1 reported recurrent and fatal subarachnoid hemorrhage from rupture of a metastatic cerebral bronchogenic aneurysm of the anterior inferior cerebellar artery. This patient also developed a mycotic neoplastic aneurysm in the contralateral anterior inferior cerebellar artery. Previous reports* of metastatic cerebral aneurysms postulated a low rate of hemorrhage. The four cases reported to date of metastatic cerebral bronchogenic aneurysm and our case, representing the fifth, have all presented with high grade subarachnoid hemorrhage. Case Report A 43-year-old female with a history of hypertension, asthma, intravenous drug abuse, hepatitis, a right apical lung nodule and a significant smoking history acutely presented to the Emergency Department complaining of speech difficulty and left sided “numbness.” Review of systems discovered a transient headache one week and one month prior to presentation. Physical examination demonstrated 4 out of 5 strength in the left upper and lower extremity on the left with hyperreflexia and an ipsilateral Babinski sign. * circa 2000 Figure 1 Metastatic cerebral artery aneurysm. Complete cross section of aneurysm entirely occluded by partially necrotic metastatic bronchogenic carcinoma. Immunohistochemical stain for cytokeratin CK7, original magnification 40X. 1 Randazzo et al.: Metastatic MCA Aneurysm Caused by Tumor Embolus Produced by The Berkeley Electronic Press, 2009 14 JHN JOURNAL CT of the head was significant for Grade IV subarachnoid hemorrhage and a small intracerebral hemorrhage. A transfemoral cerebral angiogram revealed a right distal middle cerebral artery aneurysm. No other aneurysms were discovered. Subsequently, the patient underwent a right pterional craniotomy with excision of a right middle cerebral artery aneurysm. The resected portion of the middle cerebral artery sent to the pathology lab was i.dentified as a highly anaplastic intraluminal neoplasm that was likely metastatic in origin. Immunohistochemical staining was strongly positive for cytokeratins AE1, CK7 (Figure 1) and CAM5.2 (Figure 2). Hematoxylin and eosin staining demonstrated tumor embolus with invasion through the internal elastic membrane of the middle cerebral artery (Figure 3). Based on these results and the patient’s known lung nodule, it was concluded that the specimen represented a metastatic carcinoma most likely from the lung. A multi-disciplinary team was assembled to further investigate and treat the patient for a primary lung carcinoma. The final impression of the oncologist was that the patient’s metastatic anaplastic carcinoma was most likely from her lung. The patient underwent whole brain irradiation and thoracic surgery was consulted for an open lung biopsy. Discussion Cerebral aneurysms due to metastatic tumor emboli are quite rare. In Ho’s2 early 1982 report of metastatic cerebral aneurysm of bronchogenic origin, he notes 23 documented cases of non-bronchogenic cerebral metastatic aneurysms. Approximately 70% of these cases were due to cardiac myxomas and 22% from choriocarcinomas. Since the publication of this article there have been three other cases of metastatic lung cancer causing cerebral aneurysms3-5. The currently reported case represents the fifth individual. The small number of cases which have been reported limit our ability to characterize these metastatic aneurysms (Table 1). The documented cases do not demonstrate gender or age as risk factors for the development of these aneurysms. Additionally, the histologic subtype of bronchogenic carcinoma does not appear to favor neoplastic aneurysms, as both squamous and small-cell lung carcinoma have been identified in tumor emboli. It is not evident that a particular artery or location has a greater chance of developing a neoplastic aneurysm. One observation that is clear is that all of the reported cases have been complicated by hemorrhage. It is unclear whether it is an inherent property of the primary carcinoma that results in hemorrhage or if observation bias results in the discovery of these aneurysms only when they bleed. If these aneurysms were often present without bleeding; however, they would most likely be reported in postmortem studies as have emboli from cardiac myxomas and choriocarcinomas. Conclusion The present case represents a rare, yet docu- mented complication of primary bronchogenic carcinoma. Since the first case was described by Ho in 1982, several other cases have been iden- tified. The limited number of cases prohibits identification of clear patterns. The recognition of neoplastic aneurysm formation as a devastat- ing complication of bronchogenic carcinoma is necessary in the differential diagnosis of mycotic aneurysms. References 1. Gliemroth J, Nowak G, Kehler U, Arnold H, Gaebel C: Neoplastic cerebral aneurysm from metastatic lung adeno- carcinoma associated with cerebral thrombosis and recurrent subarachnoid haemorrhage. J Neurol Neurosurg Psychiatry 66: 246-247, 1999. 2. Ho KL: Neoplastic aneurysm and intracranial hemorrhage. Cancer 50: 2935-2940, 1982. 3. Kochi N, Tani E, Yokota M, Nakaya Y: Neoplastic cerebral aneurysm from lung cancer. Case report. J Neurosurg 60: 640-643, 1984. 4. Murata J, Sawamura Y, Takahashi A, Abe H, Saitoh H: Intracerebral hemorrhage caused by a neoplastic aneurysm from small-cell lung carcinoma: case report. Neurosurgery 32: 124-126, 1993. 5. Olmsted WW, McGee TP: The pathogenesis of peripheral aneurysms of the central nervous system: a subject review from the AFIP. Radiology 123: 661-666, 1977. 6. Pullar M, Blumbergs PC, Phillips GE, Carney PG: Neoplastic cerebral aneurysm from metastatic gestational choriocarci- noma. Case report. J Neurosurg 63: 644-647, 1985. 7. Weir B, MacDonald N, Mielke B: Intracranial vascular compli- cations of choriocarcinoma. Neurosurgery 2: 138-142, 1978. Figure 2 Metastatic cerebral artery aneurysm. Tumor embolus adherent to wall of artery. Immunohistochemical stain for cytokeratin CAM5.2, original magnification 200X. Figure 3 Metastatic cerebral artery aneurysm. Tumor embolus with invasion through internal elastic membrane Table 1. Author Demographics Type of Cancer Location Complications Ho (2) 68, male Bronchogenic Right Posterior Hemorrhage, Cerebral A. Rupture Murata et al (4) 63, male Small Cell (lung) Anomalous Hematoma Artery Kochi et al (3) 56, male Undifferentiated Left Posterior Hematoma, Squamous Cell (lung) Temporal A. Rupture Gliemroth et al (1) 38, female Adenocarcinoma Bilateral Anterior Hematoma (lung) Inferior Cerebellar A. Rupture Current study 43, female Bronchogenic Right Middle Hemorrhage Cerebral A. 2 JHN Journal, Vol. 4 [2009], Iss. 3, Art. 6 http://jdc.jefferson.edu/jhnj/vol4/iss3/6\",\"PeriodicalId\":355574,\"journal\":{\"name\":\"JHN Journal\",\"volume\":\"17 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JHN Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.29046/JHNJ.004.3.006\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JHN Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29046/JHNJ.004.3.006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

目的与重要性:探讨支气管源性转移性脑动脉瘤的临床表现和神经病理学表现。转移性支气管源性脑动脉瘤非常罕见,仅报道与高度出血相关。临床表现:1例患者有头痛、言语困难、左侧“麻木”、左侧第七神经麻痹、左侧偏瘫病史,发现脑实质内及蛛网膜下腔出血伴右侧大脑中远端动脉动脉瘤。干预措施:翼点开颅切除真菌节段。手术标本送病理做常规组织学和免疫组织化学检查。结论:支气管源性转移性脑动脉瘤患者通常表现为蛛网膜下腔出血,这与先前观察到的“肿瘤性动脉瘤出血罕见”相反。在鉴别诊断真菌性动脉瘤时应考虑肿瘤栓子。脑动脉瘤被报道为原发性颅外肿瘤的并发症。这种病例的优势与心脏黏液瘤和绒毛膜癌有关。Olmsted和McGee5报道,左心房黏液瘤患者全身栓塞率约为45%,其中一半可能发生在大脑。Weir等7将绒毛膜癌引起的真菌性动脉瘤具体描述为远端、分叶状和梭状。Pullar等6报道了8例继发于绒毛膜癌的转移性脑动脉瘤。目前仅报道过4例支气管源性转移性脑动脉瘤1-4,第一例由Ho2于1982年报道。何描述了一个致命的脑出血与动脉瘤在内侧方面的枕叶。组织学上,血管腔内含有肿瘤细胞集合,这些肿瘤细胞侵入血管壁,破坏了原有的细胞结构。Kochi等人3报道了左侧颞后动脉皮质分支转移性脑支气管源性动脉瘤破裂引起的脑内血肿。Murata等人4报道了脑后动脉皮质分支转移性脑支气管源性动脉瘤破裂引起的脑内血肿。Gliemroth等报道了小脑前下动脉转移性脑支气管源性动脉瘤破裂引起的复发性和致命的蛛网膜下腔出血。该患者在对侧小脑前下动脉也出现了真菌性肿瘤动脉瘤。先前关于转移性脑动脉瘤的报道认为出血率很低。迄今为止报道的四例转移性脑支气管源性动脉瘤和我们的病例,代表第五例,都表现为高度蛛网膜下腔出血。病例报告一名43岁女性,有高血压、哮喘、静脉药物滥用、肝炎、右肺根尖结节和明显的吸烟史,以言语困难和左侧“麻木”急性就诊于急诊科。在就诊前一周和一个月复查发现短暂性头痛。体格检查显示左上肢和左下肢的5个力量中有4个具有反射性亢进和同侧Babinski征。* 2000年前后图1转移性脑动脉瘤。被部分坏死转移性支气管癌完全闭塞的动脉瘤横切面。细胞角蛋白CK7免疫组化染色,原放大倍数40X。1 Randazzo等人:由肿瘤栓子引起的转移性MCA动脉瘤,伯克利电子出版社,2009 14 JHN JOURNAL头部CT显示蛛网膜下腔出血IV级和小脑出血。经股脑血管造影显示右侧远端大脑中动脉动脉瘤。没有发现其他动脉瘤。随后,患者接受了右侧翼点开颅手术,切除了右侧大脑中动脉瘤。被切除的大脑中动脉送至病理实验室后被鉴定为高度间变性的腔内肿瘤,可能起源于转移性肿瘤。免疫组化染色显示细胞角蛋白AE1、CK7(图1)和CAM5.2(图2)呈强阳性。苏木精和伊红染色显示肿瘤栓子侵入大脑中动脉内弹性膜(图3)。基于这些结果和患者已知的肺结节,我们认为该标本很可能是肺转移癌。一个多学科的团队被召集来进一步调查和治疗原发性肺癌患者。 肿瘤学家最后的结论是病人的转移性间变性癌很可能来自她的肺部。患者接受了全脑照射和胸外科手术,进行了开放式肺活检。由转移性肿瘤栓塞引起的脑动脉瘤是相当罕见的。在Ho 1982年早期关于支气管源性脑转移动脉瘤的报告中,他记录了23例非支气管源性脑转移动脉瘤。这些病例中大约70%是由于心脏黏液瘤,22%是由于绒毛膜癌。自这篇文章发表以来,已经有另外三个转移性肺癌导致脑动脉瘤的病例3-5。目前报告的病例是第五例。已报道的病例数量少,限制了我们对这些转移性动脉瘤进行特征描述的能力(表1)。记录在案的病例并未证明性别或年龄是这些动脉瘤发生的危险因素。此外,支气管源性癌的组织学亚型似乎不倾向于肿瘤性动脉瘤,因为鳞状和小细胞肺癌都已在肿瘤栓塞中被发现。目前尚不清楚某一特定动脉或部位是否更容易发生肿瘤性动脉瘤。有一点很清楚,所有报告的病例都伴有出血。目前尚不清楚是原发性癌的固有特性导致出血,还是观察偏差导致这些动脉瘤只有在出血时才被发现。如果这些动脉瘤经常没有出血;然而,在死后的研究中,他们最有可能被报道为心脏黏液瘤和绒毛膜癌引起的栓塞。结论本病例为罕见的原发性支气管源性癌并发症。自何氏于1982年描述了第一例以来,已经发现了其他几个病例。由于案例数量有限,无法确定明确的模式。在鉴别诊断真菌性动脉瘤时,必须认识到肿瘤性动脉瘤是支气管源性癌的致命并发症。引用1。王晓明,王晓明,王晓明,等。肺腺癌转移性脑动脉瘤与脑血栓形成及蛛网膜下腔出血的相关性研究。中华神经外科杂志,21(3):387 - 398。2. 何克立:肿瘤性动脉瘤与颅内出血。巨蟹座:2935-29403.李建军,李建军,李建军,等:肺癌脑动脉瘤的诊断。病例报告。中华神经外科杂志(英文版),2004。4. Murata J, Sawamura Y, Takahashi A, Abe H, saiitoh H:小细胞肺癌致肿瘤性动脉瘤脑出血1例报告。神经外科32(2):1 - 6,1993。5. Olmsted WW, McGee TP:中枢神经系统外周动脉瘤的发病机制:来自AFIP的主题综述。中华放射学杂志(英文版),1997。6. Pullar M, Blumbergs PC, Phillips GE, Carney PG:转移性妊娠绒毛膜瘤所致的肿瘤性脑动脉瘤。病例报告。中华神经外科杂志(3):644-647,1985。7. 王晓明,王晓明,王晓明,等。绒毛膜癌颅内血管并发症的研究。神经外科杂志2:138-142,1978。图2转移性脑动脉瘤。肿瘤栓子附着在动脉壁上。细胞角蛋白CAM5.2免疫组化染色,原放大倍数200X。图3转移性脑动脉瘤。经内弹性膜浸润的肿瘤栓子癌症部位并发症类型Ho(2) 68,男性支气管源性右后出血,脑A.破裂Murata等(4)63,男性小细胞(肺)异常血肿动脉Kochi等(3)56,男性未分化左后血肿,鳞状细胞(肺)颞A.破裂Gliemroth等(1)38,女性腺癌双侧前血肿(肺)小脑下A.破裂目前研究43,女性支气管源性右脑中出血[j] .中华医学杂志[2009],第4卷第3期,第6期http://jdc.jefferson.edu/jhnj/vol4/iss3/6
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A Metastatic Middle Cerebral Artery Aneurysm Caused by an Intraluminal Bronchogenic Tumor Embolus
Objective and Importance: To describe the clinical presentation and neuropathological findings of metastatic cerebral aneurysms of bronchogenic origin. Metastatic bronchogenic cerebral aneurysms are exceptionally rare and have only been reported in association with high grade hemorrhage. Clinical Presentation: One patient presenting with a history of headache, speech difficulty, left-sided “numbness”, left seventh nerve palsy and left hemiparesis was found to have intraparenchymal and subarachnoid hemorrhage with an aneurysm of the right distal Sylvian middle cerebral artery. Intervention: Pterional craniotomy with excision of mycotic segment. Surgical specimen sent to pathology for routine histology and immunohistochemistry. Conclusion: Patients with metastatic cerebral aneuryms of bronchogenic origin usually present with subarachnoid hemorrhage, contrary to prior observations that “hemorrhage from neoplasia-induced aneurysms is paradoxically rare.” A tumor embolus should be considered in the differential diagnosis of a mycotic aneurysm. Cerebral aneurysms have been reported as a complication of primary extracranial neoplasms. The preponderance of such cases has been associated with cardiac myxomas and choriocarcinomas. Olmsted and McGee5 report approximately a 45% systemic embolization rate, half of which may be cerebral, in patients with left atrial myxoma. Weir et al.7 described mycotic aneurysms from choriocarcinoma as specifically being distal, lobulated, and fusiform. Pullar et al.6 reported a series of eight cases of metastatic cerebral aneurysms secondary to choriocarcinoma. There have only been four reported cases of metastatic cerebral aneurysm of bronchogenic origin1-4 The first case was described in 1982 by Ho2. Ho described a fatal intracerebral hemorrhage associated with an aneurysm in the medial aspect of the occipital lobe. Histologically, the lumen of the vessel contained collections of neoplastic cells that had invaded the vessel wall and destroyed the native cytoarchitecture. Kochi et al.3 described an intracerebral hematoma from rupture of a metastatic cerebral bronchogenic aneurysm in a cortical branch of the left posterior temporal artery. Murata et al.4 reported intracerebral hematoma from rupture of a metastatic cerebral bronchogenic aneurysm from a cortical branch of the posterior cerebral artery. Gliemroth et al.1 reported recurrent and fatal subarachnoid hemorrhage from rupture of a metastatic cerebral bronchogenic aneurysm of the anterior inferior cerebellar artery. This patient also developed a mycotic neoplastic aneurysm in the contralateral anterior inferior cerebellar artery. Previous reports* of metastatic cerebral aneurysms postulated a low rate of hemorrhage. The four cases reported to date of metastatic cerebral bronchogenic aneurysm and our case, representing the fifth, have all presented with high grade subarachnoid hemorrhage. Case Report A 43-year-old female with a history of hypertension, asthma, intravenous drug abuse, hepatitis, a right apical lung nodule and a significant smoking history acutely presented to the Emergency Department complaining of speech difficulty and left sided “numbness.” Review of systems discovered a transient headache one week and one month prior to presentation. Physical examination demonstrated 4 out of 5 strength in the left upper and lower extremity on the left with hyperreflexia and an ipsilateral Babinski sign. * circa 2000 Figure 1 Metastatic cerebral artery aneurysm. Complete cross section of aneurysm entirely occluded by partially necrotic metastatic bronchogenic carcinoma. Immunohistochemical stain for cytokeratin CK7, original magnification 40X. 1 Randazzo et al.: Metastatic MCA Aneurysm Caused by Tumor Embolus Produced by The Berkeley Electronic Press, 2009 14 JHN JOURNAL CT of the head was significant for Grade IV subarachnoid hemorrhage and a small intracerebral hemorrhage. A transfemoral cerebral angiogram revealed a right distal middle cerebral artery aneurysm. No other aneurysms were discovered. Subsequently, the patient underwent a right pterional craniotomy with excision of a right middle cerebral artery aneurysm. The resected portion of the middle cerebral artery sent to the pathology lab was i.dentified as a highly anaplastic intraluminal neoplasm that was likely metastatic in origin. Immunohistochemical staining was strongly positive for cytokeratins AE1, CK7 (Figure 1) and CAM5.2 (Figure 2). Hematoxylin and eosin staining demonstrated tumor embolus with invasion through the internal elastic membrane of the middle cerebral artery (Figure 3). Based on these results and the patient’s known lung nodule, it was concluded that the specimen represented a metastatic carcinoma most likely from the lung. A multi-disciplinary team was assembled to further investigate and treat the patient for a primary lung carcinoma. The final impression of the oncologist was that the patient’s metastatic anaplastic carcinoma was most likely from her lung. The patient underwent whole brain irradiation and thoracic surgery was consulted for an open lung biopsy. Discussion Cerebral aneurysms due to metastatic tumor emboli are quite rare. In Ho’s2 early 1982 report of metastatic cerebral aneurysm of bronchogenic origin, he notes 23 documented cases of non-bronchogenic cerebral metastatic aneurysms. Approximately 70% of these cases were due to cardiac myxomas and 22% from choriocarcinomas. Since the publication of this article there have been three other cases of metastatic lung cancer causing cerebral aneurysms3-5. The currently reported case represents the fifth individual. The small number of cases which have been reported limit our ability to characterize these metastatic aneurysms (Table 1). The documented cases do not demonstrate gender or age as risk factors for the development of these aneurysms. Additionally, the histologic subtype of bronchogenic carcinoma does not appear to favor neoplastic aneurysms, as both squamous and small-cell lung carcinoma have been identified in tumor emboli. It is not evident that a particular artery or location has a greater chance of developing a neoplastic aneurysm. One observation that is clear is that all of the reported cases have been complicated by hemorrhage. It is unclear whether it is an inherent property of the primary carcinoma that results in hemorrhage or if observation bias results in the discovery of these aneurysms only when they bleed. If these aneurysms were often present without bleeding; however, they would most likely be reported in postmortem studies as have emboli from cardiac myxomas and choriocarcinomas. Conclusion The present case represents a rare, yet docu- mented complication of primary bronchogenic carcinoma. Since the first case was described by Ho in 1982, several other cases have been iden- tified. The limited number of cases prohibits identification of clear patterns. The recognition of neoplastic aneurysm formation as a devastat- ing complication of bronchogenic carcinoma is necessary in the differential diagnosis of mycotic aneurysms. References 1. Gliemroth J, Nowak G, Kehler U, Arnold H, Gaebel C: Neoplastic cerebral aneurysm from metastatic lung adeno- carcinoma associated with cerebral thrombosis and recurrent subarachnoid haemorrhage. J Neurol Neurosurg Psychiatry 66: 246-247, 1999. 2. Ho KL: Neoplastic aneurysm and intracranial hemorrhage. Cancer 50: 2935-2940, 1982. 3. Kochi N, Tani E, Yokota M, Nakaya Y: Neoplastic cerebral aneurysm from lung cancer. Case report. J Neurosurg 60: 640-643, 1984. 4. Murata J, Sawamura Y, Takahashi A, Abe H, Saitoh H: Intracerebral hemorrhage caused by a neoplastic aneurysm from small-cell lung carcinoma: case report. Neurosurgery 32: 124-126, 1993. 5. Olmsted WW, McGee TP: The pathogenesis of peripheral aneurysms of the central nervous system: a subject review from the AFIP. Radiology 123: 661-666, 1977. 6. Pullar M, Blumbergs PC, Phillips GE, Carney PG: Neoplastic cerebral aneurysm from metastatic gestational choriocarci- noma. Case report. J Neurosurg 63: 644-647, 1985. 7. Weir B, MacDonald N, Mielke B: Intracranial vascular compli- cations of choriocarcinoma. Neurosurgery 2: 138-142, 1978. Figure 2 Metastatic cerebral artery aneurysm. Tumor embolus adherent to wall of artery. Immunohistochemical stain for cytokeratin CAM5.2, original magnification 200X. Figure 3 Metastatic cerebral artery aneurysm. Tumor embolus with invasion through internal elastic membrane Table 1. Author Demographics Type of Cancer Location Complications Ho (2) 68, male Bronchogenic Right Posterior Hemorrhage, Cerebral A. Rupture Murata et al (4) 63, male Small Cell (lung) Anomalous Hematoma Artery Kochi et al (3) 56, male Undifferentiated Left Posterior Hematoma, Squamous Cell (lung) Temporal A. Rupture Gliemroth et al (1) 38, female Adenocarcinoma Bilateral Anterior Hematoma (lung) Inferior Cerebellar A. Rupture Current study 43, female Bronchogenic Right Middle Hemorrhage Cerebral A. 2 JHN Journal, Vol. 4 [2009], Iss. 3, Art. 6 http://jdc.jefferson.edu/jhnj/vol4/iss3/6
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