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Right hepatectomy for giant cavernous hemangioma with diffuse hemangiomatosis around Glisson's capsule 被引量:2
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作者 Yu Ohkura Masaji Hashimoto +3 位作者 Seigi Lee Kazunari Sasaki Masamichi Matsuda Goro Watanabe 《World Journal of Gastroenterology》 SCIE CAS 2014年第25期8312-8316,共5页
Diffuse liver hemangiomatosis with giant cavernous hemangioma in adult is extremely rare. A 35 year-old woman presented to hospital with main complaint of epigastric pain and abdominal fullness. An enhanced computed t... Diffuse liver hemangiomatosis with giant cavernous hemangioma in adult is extremely rare. A 35 year-old woman presented to hospital with main complaint of epigastric pain and abdominal fullness. An enhanced computed tomography scan revealed a massive liver tumor in right lobe about 150 mm in size. There was contrast enhancement at the periphery of the mass consistent with a cavernous hemangioma. She underwent right hepatectomy. Histologically, it was diagnosed as a cavernous hemangioma. And also, hemangiomatous lesions were scattered around the Glisson&#x02019;s capsule on the back ground liver. These hemangiomatous lesions were not recognized preoperatively. Even if we couldn&#x02019;t diagnose hemangiomatosis around the main giant hemangioma preoperatively, we need to take enough surgical margins because the giant hemangioma has the potential to have small hemangiomatous lesions around the tumor. We reported right hepatectomy for giant cavernous hemangioma with diffuse hepatic hemangiomatosis without an extrahepatic lesion in an adult. 展开更多
关键词 Giant cavernous hemangioma hemangiomatosis Right hepatectomy Around Glisson’ s capsule SURGERY
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Clinical features and imaging findings in pulmonary capillary hemangiomatosis: report of two cases and a pooled analysis 被引量:1
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作者 XIE Wan-mu DAI Hua-ping +4 位作者 JIN Mu-lan WANG Zhen YANG Yuan-hua ZHAI Zhen-guo WANG Chen 《Chinese Medical Journal》 SCIE CAS CSCD 2012年第17期3069-3073,共5页
Background Pulmonary capillary hemangiomatosis (PCH) is a rare disease and no Chinese case has been reported yet. The disease is often misdiagnosed and its clinical characteristics are incompletely described. The ai... Background Pulmonary capillary hemangiomatosis (PCH) is a rare disease and no Chinese case has been reported yet. The disease is often misdiagnosed and its clinical characteristics are incompletely described. The aim of this study was to describe two Chinese cases and to clarify the clinical and radiographic parameters of patients with PCH. Methods Two PCH cases were presented and other cases were searched from the English literature. All available clinical and radiographic data were collected from 62 literature reported PCH cases. A pooled analysis of total 64 cases was made. Results Dyspnea and hemoptysis were the most common clinical symptoms of PCH. Pulmonary hypertension (PH) was found in 78% of the reported cases. PCH typically showed characteristic diffuse or patchy ground-glass opacities (GGOs) and/or multiple ill-defined centrilobular nodules in the computed tomography. Conclusions The diagnosis of PCH requires a high clinical suspicion. However, both clinical presentations and radiographic studies often provide clues to the diagnosis, which may prompt early lung biopsy for a definite diagnosis. 展开更多
关键词 pulmonary capillary hemangiomatosis pulmonary hypertension lung biopsy
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Peritoneal cavernous hemangiomatosis:A case report
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作者 Li-Yuan Fu Hong-Yu Chen +1 位作者 Xiao-Li Diao Zhen-Jun Wang 《World Journal of Clinical Cases》 SCIE 2019年第4期489-493,共5页
BACKGROUND Cavernous hemangiomatosis in the liver and spleen has been reported, but it occurs less commonly in the peritoneum. Here we report a case of peritoneal cavernous hemangiomatosis and share some valuable info... BACKGROUND Cavernous hemangiomatosis in the liver and spleen has been reported, but it occurs less commonly in the peritoneum. Here we report a case of peritoneal cavernous hemangiomatosis and share some valuable information about this disease.CASE SUMMARY A 57-year-old Chinese man had a huge abdominal mass with abdominal distention and a significant reduction of food consumption. An enhanced abdominal and pelvic computed tomography and positron emission tomography–computed tomography revealed multiple cystic masses on the peritoneum, greater omentum, small intestinal mesentery and the surface of the spleen, and a high maximum standardized uptake value of the largest cystic lesion. Exploratory laparotomy was performed, and multiple cystic masses were found on the surface of the peritoneum, greater omentum, mesentery of the small intestine, and surface of the liver and spleen. Dark red bloody cystic fluid was present in the cystic tumor. Pathological examination showed that in the stromal components, the irregular vascular wall was thin. The vessel lumen was interlinked, and the lumen was lined with flat endothelium. According to the intraoperative findings and pathologic results, the patient was diagnosed with peritoneal cavernous hemangiomatosis.CONCLUSION The possibility of peritoneal cavernous hemangiomatosis should be considered when multiple cystic masses are found in the abdominal cavity by preoperative examination. 展开更多
关键词 PERITONEUM hemangiomatosis CAVERNOUS hemangiomatosis CYSTIC LESION Case report
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磁共振磁敏感加权序列对儿童脑内海绵状血管瘤的诊断价值 被引量:1
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作者 董世杰 李欣 +1 位作者 时胜利 郑彬 《实用医学影像杂志》 2022年第5期493-495,共3页
目的探讨磁共振磁敏感加权(SWI)序列对儿童脑内海绵状血管瘤的诊断价值。方法回顾性分析2017年8月至2018年8月河南省儿童医院经病理证实并于术前进行颅脑磁共振常规及SWI序列扫描的颅内海绵状血管瘤患者22例,分析其磁共振常规序列及SWI... 目的探讨磁共振磁敏感加权(SWI)序列对儿童脑内海绵状血管瘤的诊断价值。方法回顾性分析2017年8月至2018年8月河南省儿童医院经病理证实并于术前进行颅脑磁共振常规及SWI序列扫描的颅内海绵状血管瘤患者22例,分析其磁共振常规序列及SWI序列影像表现。结果22例患儿于T_(1)加权序列(T_(1)WI)发现病灶数28个,病灶直径为0.5~11.2 mm,平均(6.4±1.8)mm;于T_(2)加权序列(T_(2)WI)发现病灶数35个,病灶直径为0.5~14.6 mm,平均(7.1±1.7)mm;于SWI序列发现病灶数为66个,病灶直径为0.5~25.8 mm,平均(14.3±1.8)mm;T_(1)WI与T_(2)WI序列病灶平均直径相比较,差异无统计学意义(P>0.05),SWI与T_(1)WI、T_(2)WI序列病灶平均直径相比较,差异有统计学意义(P<0.05)。结论磁共振SWI序列较常规序列更能清楚显示儿童颅内海绵状血管瘤病灶。 展开更多
关键词 血管癌 海绵状 磁共振成像 儿童
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Pulmonary Capillary Hemangiomatosis Associated with CREST Syndrome: A Challenge of Diagnosis and Treatment 被引量:2
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作者 Xiao-Li Diao Xiang-Dong Mu Mu-Lan Jin 《Chinese Medical Journal》 SCIE CAS CSCD 2017年第21期2645-2646,共2页
To the Editor: A 65-year-old woman with calcinosis, Raynaud&#39;s phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome was admitted to hospital because of progressive dyspnea on e... To the Editor: A 65-year-old woman with calcinosis, Raynaud&#39;s phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome was admitted to hospital because of progressive dyspnea on exertion for about 1 year. In the past, she had been diagnosed as gastroesophageal reflux disease and scleroderma for 10 years. Physical examination showed masked face, Raynaud's phenomenon, finger sclerodactyly, and skin telangiectasia on her neck and back [Figure 1a and 1b]. The titer of anticentromere antibody in serum increased to 1: 1000. Analysis of arterial gas on room air revealed the partial pressure of arterial oxygen (PaO2) was 54 mmHg (1 mmHg = 0.133 kPa) and carbon dioxide (PaCO2) was 32 mmHg. Echocardiogram showed severe tricuspid regurgitation and elevated pulmonary arterial pressure of 78 mmHg. 展开更多
关键词 CREST Syndrome Pulmonary Capillary hemangiomatosis Associated
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Right colon and liver hemangiomatosis:A case report and a review of the literature 被引量:1
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作者 Athanasios Marinis Evi Kairi +2 位作者 Theodosios Theodosopoulos Agathi Kondi-Pafiti Vassilios Smyrniotis 《World Journal of Gastroenterology》 SCIE CAS CSCD 2006年第39期6405-6407,共3页
Cavernous hemangiomatosis of the colon and liver in a 38-year-old woman presenting with a history of cramp like abdominal pain and a mass in the right iliac fossa are presented. Abdominal ultrasonography and computed ... Cavernous hemangiomatosis of the colon and liver in a 38-year-old woman presenting with a history of cramp like abdominal pain and a mass in the right iliac fossa are presented. Abdominal ultrasonography and computed tomography demonstrated multiple liver hemangiomas as well as a noncystic lesion in the right iliac fossa. Operative findings were suggestive of diffuse hemangiomatosis of the right colon and an extensive right hemicolectomy was performed. A review of the literature is presented, considering current diagnostic and therapeutic methods. 展开更多
关键词 hemangiomatosis Right Colon LIVER
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Splenic hemangiopericytoma and serosal cavernous hemangiomatosis of the adjacent colon 被引量:1
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作者 Tuncay Yilmazlar Turkay Kirdak +3 位作者 Omer Yerci Saduman B.Adim Ozkan Kanat Osman Manavoglu 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第26期4111-4113,共3页
A healthy 31-years-old man presented with a three-year history of abdominal discomfort. Radiological examinations revealed multifocal tumoral lesions in the spleen. The patient underwent splenectomy for differential d... A healthy 31-years-old man presented with a three-year history of abdominal discomfort. Radiological examinations revealed multifocal tumoral lesions in the spleen. The patient underwent splenectomy for differential diagnosis and treatment. During the operation, in addition to the splenic masses, there were also multiple milimetric purpuric-like lesions on the colonic serosal surfaces adjacent to the splenic hilus. One of them was excised. Histologic examination showed hemangiopericytoma of the spleen and cavernous hemangioma of the adjacent colon. This is the first report showing the close association of these two distinct lesions with vascular origin in the literature. Despite not having any apparent evidence, there may be a sequential relationship between the hemangiopericytoma of the spleen and cavernous hemangiomas. 展开更多
关键词 Hemangiopericytoma of the spleen Cavernous hemangiomatosis
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弥漫性新生儿血管瘤病伴心衰1例并文献回顾
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作者 卫风蕾 程宪 +1 位作者 王恒娟 牛红喜 《中国皮肤性病学杂志》 CAS 北大核心 2014年第1期62-64,共3页
患儿女,14d。患儿周身发现针头大红色斑疹11d,逐渐增多增大。皮肤科情况:患儿颜面部、胸部、背部、臀部、四肢、双手、足可见数十个针头至绿豆大鲜红色斑丘疹,质地柔软,界限清楚。右耳处可见一3cm×4cm大鲜红色斑。肝脏B超可见不规... 患儿女,14d。患儿周身发现针头大红色斑疹11d,逐渐增多增大。皮肤科情况:患儿颜面部、胸部、背部、臀部、四肢、双手、足可见数十个针头至绿豆大鲜红色斑丘疹,质地柔软,界限清楚。右耳处可见一3cm×4cm大鲜红色斑。肝脏B超可见不规则低回声区,肝脏增强CT示多发性大小不等边界欠清低密度灶。肝脏血管重建提示存在动静脉短路。诊断:弥漫性新生儿血管瘤病。入院后给予强的松,血管瘤进行性增多、增大,并出现充血性心力衰竭,故给予甲强龙、美托洛尔联合抗心衰治疗,患儿病情逐渐好转、稳定。心衰稳定后将美托洛尔换用普萘洛尔治疗。 展开更多
关键词 心衰 血管瘤病 甲强龙 美托洛尔 普萘洛尔
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成人弥漫性肝血管瘤病
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作者 徐菲 孙文兵 高君 《中华肝胆外科杂志》 CAS CSCD 北大核心 2024年第5期390-395,共6页
成人弥漫性肝血管瘤病(DHH)是一种极罕见的良性疾病。成人DHH可局限于肝脏的一段或几段,也可弥漫性分布于整个肝脏;还可能同时累及肝外其他器官。由于成人DHH发病率低,临床认识不足,容易误诊。不同类型成人DHH治疗原则不同,预后也不尽... 成人弥漫性肝血管瘤病(DHH)是一种极罕见的良性疾病。成人DHH可局限于肝脏的一段或几段,也可弥漫性分布于整个肝脏;还可能同时累及肝外其他器官。由于成人DHH发病率低,临床认识不足,容易误诊。不同类型成人DHH治疗原则不同,预后也不尽相同。本文对成人DHH的流行病学、发病机制、诊断、治疗和预后进行综述。 展开更多
关键词 成年人 弥漫性肝血管瘤病 发病机制 诊断 治疗
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双能量CT成像技术在肺血管疾病中的应用进展
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作者 丁兆慧 奚群英 《心血管病学进展》 CAS 2024年第1期27-30,共4页
双能量CT(DECT)应用两种能量、两套探测器,根据不同能量下物质衰减特性的差异进行定性及定量的数据采集。DECT具有高分辨率、易获得等优势,通过后处理技术,从形态学、功能学两方面获取疾病信息。近年来,DECT在肺血管疾病如肺栓塞、慢性... 双能量CT(DECT)应用两种能量、两套探测器,根据不同能量下物质衰减特性的差异进行定性及定量的数据采集。DECT具有高分辨率、易获得等优势,通过后处理技术,从形态学、功能学两方面获取疾病信息。近年来,DECT在肺血管疾病如肺栓塞、慢性血栓栓塞性肺动脉高压、动脉型肺动脉高压、肺静脉闭塞性疾病/肺毛细血管瘤等诊治中展现出优越的作用。现从DECT的技术原理及其在肺血管疾病中的应用进展做一综述。 展开更多
关键词 双能量CT 肺灌注成像 肺栓塞 慢性血栓栓塞性肺动脉高压 动脉型肺动脉高压 肺静脉闭塞性疾病/肺毛细血管瘤
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肺毛细血管瘤病1例及文献回顾 被引量:2
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作者 熊焰 李晓霞 +3 位作者 牟向东 李东 王颖 李挺 《北京大学学报(医学版)》 CAS CSCD 北大核心 2015年第5期865-869,共5页
报道1例肺毛细血管瘤病((pulmonary capillary hemangiomatosis,PCH),结合本例特点复习国内外文献报道和2008年WHO在Dana Point制定的肺高压临床分类,对该病的诊断、鉴别诊断以及病因和治疗进行介绍,提高各科医生对这一罕见病的认识。... 报道1例肺毛细血管瘤病((pulmonary capillary hemangiomatosis,PCH),结合本例特点复习国内外文献报道和2008年WHO在Dana Point制定的肺高压临床分类,对该病的诊断、鉴别诊断以及病因和治疗进行介绍,提高各科医生对这一罕见病的认识。本例患者为中年女性,主要临床症状为活动后气促;右心导管检查示中度肺动脉高压;CT肺血管造影(CT pulmonary angiography,CTPA)示双肺弥漫磨玻璃密度小叶核心结节,肺动脉主干及分支增宽;组织病理学上表现为肺小动脉肌化,肌性肺动脉中膜增厚,肺泡壁毛细血管显著增生呈多排、结节状及片状;患者药物治疗无效,于3个月后死亡。PCH是一种罕见、预后不良的血管病变,其诊断需要综合临床、影像及组织病理3方面的资料,组织病理学检查是最可靠的手段,对确诊具有决定性作用。该病在临床、影像及组织形态上均与肺静脉阻塞病(pulmonary veno-occlusive disease,PVOD)存在诸多相似和交叉之处,两者需要重点鉴别。在诸多病理学改变中,肺泡壁毛细血管增生是PCH最重要的特点,也是与PVOD相鉴别的关键点。肺移植被认为是PCH唯一有效的治疗手段,如果不及时进行,患者通常在确诊后几个月内死亡。 展开更多
关键词 肺毛细血管瘤病 肺静脉闭塞性疾病 肺动脉高压
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脑膜血管瘤病伴癫痫的临床特点分析
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作者 陈俊喜 王艮波 +7 位作者 张伟 周修明 谭红平 刘妲 吴玉鹏 王展航 郭强 朱丹 《临床神经外科杂志》 2022年第6期689-692,698,共5页
目的总结脑膜血管瘤病的临床特点、治疗经验及预后。方法回顾性分析广东三九脑科医院2016年6月—2021年1月期间收治的6例脑膜血管瘤病患者的临床资料,并结合相关文献进行复习。结果6例患者中,临床发作表现为全身强直阵挛发作1例,部分发... 目的总结脑膜血管瘤病的临床特点、治疗经验及预后。方法回顾性分析广东三九脑科医院2016年6月—2021年1月期间收治的6例脑膜血管瘤病患者的临床资料,并结合相关文献进行复习。结果6例患者中,临床发作表现为全身强直阵挛发作1例,部分发作继发全身强直阵挛发作5例。术中皮层监测提示所有患者病变部位有癫痫样放电,均在术中皮层脑电图监测引导下行病灶+病灶周围皮层致痫灶切除手术治疗。术后均给予抗癫痫药物治疗,术后Engel分级均为Ⅰ级,术后近期及远期均无明显并发症出现。结论反复癫痫发作的患者,如果颅脑MRI提示长T_(1)长T_(2)异常信号影,T_(2)Flair呈内低外高信号影,T_(1)增强可见部分强化,CT扫描提示,钙化病变应考虑脑膜血管瘤病的诊断可能。脑膜血管瘤病经过电生理评估和多学科讨论确定致痫区后,给予病灶和周围致痫区切除术,手术疗效好,术后复发风险低,所以脑膜血管瘤病伴癫痫患者可通过手术获得良好受益,早期手术受益远远大于风险。 展开更多
关键词 脑膜血管瘤病 手术治疗 癫痫
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肺静脉闭塞病/肺毛细血管瘤病的临床特征及诊治进展
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作者 胡慧 谢军平 《南昌大学学报(医学版)》 2022年第3期73-76,83,共5页
肺毛细血管瘤病(pulmonary angiomatosis,PCH)是一种罕见的肺动脉高压(pulmonary arterial hypertension,PAH),其特征是肺泡间隔毛细血管增生。肺静脉闭塞病(pulmonary veno-occlusive disease,PVOD)组织学表现与PCH有明显的重叠,被认... 肺毛细血管瘤病(pulmonary angiomatosis,PCH)是一种罕见的肺动脉高压(pulmonary arterial hypertension,PAH),其特征是肺泡间隔毛细血管增生。肺静脉闭塞病(pulmonary veno-occlusive disease,PVOD)组织学表现与PCH有明显的重叠,被认为是同一种疾病的不同表现,归属于PCH。基因检测可使PVOD/PCH更早得到确诊,但其病程进展快,治疗无循证医学证据,预后也更差,靶向治疗部分可能导致危及生命的肺水肿,肺移植仍然是符合条件的患者唯一首选治疗方法。进一步了解PVOD/PCH的分子机制和探索新的治疗靶点是今后的研究方向。 展开更多
关键词 肺毛细血管瘤 肺静脉闭塞病 肺动脉高压 临床特征 诊断 治疗 编码真核翻译起始因子2激酶4基因
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《中国肺动脉高压诊断与治疗指南(2021版)》解读--具有明显肺静脉或肺毛细血管受累的肺动脉高压
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作者 王静 许小毛 《中国实用内科杂志》 CAS CSCD 北大核心 2022年第2期124-127,共4页
肺静脉闭塞病(PVOD)和肺毛细血管瘤病(PCH)是一类引起肺动脉高压的罕见疾病,目前统称为具有明显肺静脉或肺毛细血管受累的肺动脉高压,是动脉性肺动脉高压(PAH)中的一个亚类。这一类型肺动脉高压以肺小静脉或肺毛细血管受累为主要特点,... 肺静脉闭塞病(PVOD)和肺毛细血管瘤病(PCH)是一类引起肺动脉高压的罕见疾病,目前统称为具有明显肺静脉或肺毛细血管受累的肺动脉高压,是动脉性肺动脉高压(PAH)中的一个亚类。这一类型肺动脉高压以肺小静脉或肺毛细血管受累为主要特点,临床表现、病理特征上具有高度相似性,目前认为这两种疾病是同一种疾病的两种表现。PVOD/PCH虽然与PAH有相似的临床特征,但其预后、治疗反应与PAH不同,应用靶向药物后可能会出现肺水肿,应尽早行肺移植治疗。 展开更多
关键词 肺动脉高压 肺静脉闭塞病 肺毛细血管瘤病 解读
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肺静脉闭塞病/肺毛细血管瘤样病1例及文献复习 被引量:1
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作者 熊贤良 朱腾腾 李江 《中南大学学报(医学版)》 CAS CSCD 北大核心 2018年第5期571-576,共6页
肺静脉闭塞病(pulmonary veno-occlusive disease,PVOD)/肺毛细血管瘤样病(pulmonary capillary hemangiomatosis,PCH)是临床上罕见的引起肺动脉高压的一类肺血管疾病,其诊断需要综合临床表现、影像、肺功能、支气管镜等多方面的资料,... 肺静脉闭塞病(pulmonary veno-occlusive disease,PVOD)/肺毛细血管瘤样病(pulmonary capillary hemangiomatosis,PCH)是临床上罕见的引起肺动脉高压的一类肺血管疾病,其诊断需要综合临床表现、影像、肺功能、支气管镜等多方面的资料,治疗上尚无明确有效的药物,肺移植是目前唯一有效的治疗方案。中南大学湘雅二医院收治1例PVOD/PCH患者,现结合病例特点及相关文献报道,对该病的流行病学、病因、诊断和治疗进行介绍,以提高临床医生对这一罕见病的认识。 展开更多
关键词 肺静脉闭塞病 肺毛细血管瘤样病 肺动脉高压
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血管瘤病的X线表现 被引量:1
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作者 黄永火 戚警吾 《临床放射学杂志》 CSCD 北大核心 1994年第4期232-235,共4页
本文报道20例经病理证实的血管瘤病,它们的X线表现不全相同,甚至可出现相反的改变(如某些患骨增粗、增长,某些又萎缩变细或缩短),某些病变主要累及髓腔而某些又以骨膜改变为主;软组织的表现也可不同。结合文献,着重讨论了血... 本文报道20例经病理证实的血管瘤病,它们的X线表现不全相同,甚至可出现相反的改变(如某些患骨增粗、增长,某些又萎缩变细或缩短),某些病变主要累及髓腔而某些又以骨膜改变为主;软组织的表现也可不同。结合文献,着重讨论了血管瘤病X线改变的发病机理及与某些疾病的鉴别。 展开更多
关键词 血管瘤 X线表现 病理
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肺毛细血管瘤病与肺静脉闭塞症临床及CT特点
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作者 黎剑宇 曾庆思 《放射学实践》 北大核心 2020年第11期1419-1423,共5页
目的:分析及总结肺毛细血管瘤病(PCH)与肺静脉闭塞症(PVOD)的临床及CT影像特征。方法:回顾性分析广州医科大学附属第一医院2013-2019年经临床或病理确诊的6例PCH或PVOD患者的病例资料,其中男4例,女2例,总结其临床表现及CT征象特点,并复... 目的:分析及总结肺毛细血管瘤病(PCH)与肺静脉闭塞症(PVOD)的临床及CT影像特征。方法:回顾性分析广州医科大学附属第一医院2013-2019年经临床或病理确诊的6例PCH或PVOD患者的病例资料,其中男4例,女2例,总结其临床表现及CT征象特点,并复习相关文献对该病进行归纳分析。结果:PCH和PVOD临床症状以胸闷、气促、干咳为主,少或无咳痰、咯血。常伴有肺功能受损,以弥散功能严重下降为主,平均一氧化碳弥散量(DLCO)占预测值的百分比[DLCO(%Pred)]为(31.0±7.3)%。心脏彩超及右心导管均提示肺动脉高压。胸部CT征象常表现为多发斑片磨玻璃影、多发磨玻璃小结节影、小叶间隔增厚、肺门及纵隔淋巴结肿大、肺动脉主干增宽及右心增大等肺动脉高压表现,心包积液等,部分可见支气管动脉增粗。其中PCH以多发磨玻璃小结节影为主,小叶间隔增厚、肺门及纵隔淋巴结肿大等表现较轻,PVOD以多发斑片磨玻璃影为主,小叶间隔增厚、肺门及纵隔淋巴结肿大等表现较明显。结论:PCH和PVOD是罕见的肺血管疾病,其临床症状、肺功能检查、胸部CT表现具有一定特征。 展开更多
关键词 肺毛细血管瘤病 肺静脉闭塞症 肺动脉高压 体层摄影术 X线计算机
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