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Mycobacterium avium Complex-associated Pleural Effusion in an Immunocompetent Host : A Rare Case Report and Literature Review. 一例罕见病例报告和文献综述。
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000858
Muhammad Perwaiz, Reiichiro Obata, Ellen C Bradley
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引用次数: 0
Safety of Bilateral Whole Lung Lavage for Pulmonary Alveolar Proteinosis: Experiences in a Multicenter Cohort. 双侧全肺灌洗治疗肺泡蛋白病的安全性:多中心队列的经验。
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000897
Max T Wayne, Muhammad S Ali, Lance Roller, Steven E Gay, Fabien Maldonado, Jose De Cardenas
P ulmonary alveolar proteinosis (PAP) is a rare lung disease in which surfactant accumulates in alveolar macrophages and the distal airways, resulting in impaired gas exchange.1,2 For symptomatic patients, standard treatment is whole lung lavage to restore gas exchange.1,3 This procedure is performed under general anesthesia using a double-lumen endotracheal tube with single lung-ventilation.3,4 Warmed saline is instilled in the target lung in serial aliquots until the fluid return resembles normal lavage fluid.3 Consequently, this can take hours to perform, may be associated with hypoxemia during the procedure, and has therefore traditionally been performed as a staged procedure over multiple days (ie, 1 lung per procedure).3,4 However, some institutions have adopted techniques that allow for bilateral whole lung lavage to be performed sequentially in a single procedure, although this practice remains controversial. We describe a multicenter cohort of patients with PAP treated with bilateral whole lung lavag in a single procedural setting.
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引用次数: 0
COVID-19-Associated Tracheal Stenosis (COATS): A New Entity? COVID-19相关的气管狭窄(COATS):一个新的实体?
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000863
Rahul Tyagi, Meenakshisundaram Arunachalam, Saurabh Mittal, Vijay Hadda, Anant Mohan, Randeep Guleria, Karan Madan
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引用次数: 1
Role of Transbronchial Lung Cryobiopsy in the Diagnosis of Interstitial Lung Disease: A Meta-analysis of 68 Studies and 6300 Patients. 经支气管肺冷冻活检在间质性肺病诊断中的作用:68项研究和6300名患者的荟萃分析。
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000865
Yazan Zayed, Bashar N Alzghoul, Ryan Hyde, Zerka Wadood, Momen Banifadel, Majd Khasawneh, Phillip Brandon Maharrey, Haneen Saker, Christopher Harden, Gabrielle Barnes, Diana Gomez-Manjarres, Divya Patel, Ibrahim Faruqi, Borna Mehrad, Hiren J Mehta

Background: Diagnosis of interstitial lung disease (ILD) is based on multidisciplinary team discussion (MDD) with the incorporation of clinical, radiographical, and histopathologic information if available. We aim to evaluate the diagnostic yield and safety outcomes of transbronchial lung cryobiopsy (TBLC) in the diagnosis of ILD.

Methods: We conducted a meta-analysis by comprehensive literature search to include all studies that evaluated the diagnostic yields and/or adverse events with TBLC in patients with ILD. We calculated the pooled event rates and their 95% confidence intervals (CIs) for the diagnostic yield by MDD, histopathologic diagnostic yield, and various clinical adverse events.

Results: We included 68 articles (44 full texts and 24 abstracts) totaling 6386 patients with a mean age of 60.7±14.1 years and 56% men. The overall diagnostic yield of TBLC to achieve a definite or high-confidence diagnosis based on MDD was 82.3% (95% CI: 78.9%-85.2%) and histopathologic diagnosis of 72.5% (95% CI: 67.7%-76.9%). The overall rate of pneumothorax was 9.6% (95% CI: 7.9%-11%), while the rate of pneumothorax requiring drainage by a thoracostomy tube was 5.3% (95% CI: 4.1%-6.9%). The rate of moderate bleeding was 11.7% (95% CI: 9.1%-14.9%), while the rate of severe bleeding was 1.9% (95% CI: 1.4%-2.6%). The risk of mortality attributed to the procedure was 0.9% (95% CI: 0.7%-1.3%).

Conclusion: Among patients with undiagnosed or unclassified ILD requiring tissue biopsy for diagnosis, transbronchial cryobiopsy represents a reliable alternative to surgical lung biopsy with decreased incidence of various clinical adverse events.

背景:间质性肺病(ILD)的诊断是基于多学科团队讨论(MDD),并结合临床、放射学和组织病理学信息(如果可用)。我们的目的是评估经支气管肺冷冻活检(TBLC)在ILD诊断中的诊断率和安全性结果。方法:我们通过综合文献检索进行了荟萃分析,包括所有评估ILD患者TBLC诊断率和/或不良事件的研究。我们计算了MDD诊断率、组织病理学诊断率和各种临床不良事件的合并事件率及其95%置信区间(CI)。结果:我们纳入了68篇文章(44篇全文和24篇摘要),共6386名患者,平均年龄为60.7±14.1岁,其中56%为男性。TBLC在MDD基础上获得明确或高置信度诊断的总诊断率为82.3%(95%CI:78.9%-85.2%),组织病理学诊断为72.5%(95%CI:67.7%-76.9%),而需要经胸腔造口管引流的肺气肿发生率为5.3%(95%CI:4.1%-6.9%)、中度出血发生率为11.7%(95%CI:9.1%-14.9%),而严重出血率为1.9%(95%CI:1.4%-2.6%)。手术导致的死亡风险为0.9%(95%CI:0.7%-1.3%)。结论:在需要组织活检诊断的未诊断或未分类ILD患者中,经支气管冷冻活检是一种可靠的替代手术肺活检的方法,可降低各种临床不良事件的发生率。
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引用次数: 0
Impact of a Dedicated Pleural Clinic on Indwelling Pleural Catheter Related Outcomes: A Retrospective Single Center Experience. 专用胸膜诊所对留置胸膜导管相关结果的影响:一项回顾性单中心经验。
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000901
Katherine B Malcolm, Eric J Seeley, Yaron B Gesthalter

Background: Recurrent pleural effusions are a major cause of morbidity and frequently lead to hospitalization. Indwelling pleural catheters (IPCs) are tunneled catheters that allow ambulatory intermittent drainage of pleural fluid without repeated thoracentesis. Despite the efficacy and safety of IPCs, data supporting postplacement follow-up is limited and variable. Our study aims to characterize the impact of a dedicated pleural clinic (PC) on patient outcomes as they relate to IPCs.

Methods: Patients who underwent IPC placement between 2015 and 2021 were included in this retrospective study. Differences in outcomes were analyzed between patients with an IPC placed and managed by Interventional Pulmonology (IP) through the PC and those placed by non-IP services (non-PC providers) before and after the PC implementation.

Results: In total, 371 patients received IPCs. Since the implementation of the PC, there was an increase in ambulatory IPC placement (31/133 pre-PC vs. 96/238 post-PC; P =0.001). There were fewer admissions before IPC placement (18/103 vs. 43/133; P =0.01), and fewer thoracenteses per patient (2.7±2.5 in PC cohort vs. 4±5.1 in non-PC cohort; P <0.01). The frequency of pleurodesis was higher in the PC cohort (40/103 vs. 41/268; P <0.001). A Fine and Gray competing risks model indicated higher likelihood of pleurodesis in the PC cohort (adjusted subhazard ratio 3.8, 95% CI: 2.5-5.87).

Conclusion: Our experience suggests that the implementation of a dedicated PC can lead to improved patient outcomes including fewer procedures and admissions before IPC placement, and increased rates of pleurodesis with IPC removal.

背景:复发性胸腔积液是发病的主要原因,经常导致住院治疗。留置式胸膜导管(IPC)是一种隧道式导管,可在不重复胸腔穿刺的情况下对胸膜液进行动态间歇性引流。尽管IPCs具有疗效和安全性,但支持安置后随访的数据是有限和可变的。我们的研究旨在描述专门的胸膜诊所(PC)对患者预后的影响,因为它们与IPC有关。方法:将2015年至2021年间接受IPC植入的患者纳入本回顾性研究。在PC实施前后,分析了由介入性肺病(IP)通过PC安置和管理的IPC患者与由非IP服务(非PC提供商)安置的IPC患者之间的结果差异。结果:总共有371名患者接受了IPCs。自PC实施以来,门诊IPC安置有所增加(PC前31/133对PC后96/238;P=0.001)。IPC安置前入院人数较少(18/103对43/133;P=0.01),每位患者更少的胸腔穿刺次数(PC队列为2.7±2.5次,非PC队列为4±5.1次;P结论:我们的经验表明,实施专用PC可以改善患者的预后,包括减少IPC植入前的手术和入院次数,并提高IPC切除后的胸膜固定率。
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引用次数: 3
O-arm CT for Confirmation of Successful Navigation During Robotic Assisted Bronchoscopy. O型臂CT在机器人辅助支气管镜检查中用于确认导航成功。
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000894
Jefferson Chambers, Daniel Knox, Timothy Leclair

Background: Robotic assisted bronchoscopy (RAB) is designed to increase bronchoscopic accessibility for difficult to reach pulmonary lesions. One limitation to success of RAB is computed tomography (CT) to body divergence. Real time imaging with cone beam CT is increasingly utilized for confirmation of correct navigation and tool-in-lesion during RAB. O-arm CT is a 3-dimensional imaging modality, which has not previously been described for use with RAB. Our purpose is to display the feasibility, ease of use, and high rate of confirmation of tool-in-lesion when using O-arm CT during RAB.

Methods: Single center, retrospective review of 75 patients undergoing RAB with intraprocedural use of O-arm CT.

Results: Median patient age was 65 years. Forty-nine percent of cases involved nodules ≤2 cm. Bronchus sign was absent in 44% of cases. Median procedure time was 80 minutes. Median number of O-arm CT runs per case was 2. The median effective dose of radiation was 7.2 millisieverts. Tool-in-lesion was confirmed in 97% (77 of 79) of cases. Definitive diagnosis was reached in 61 to 68 of 79 cases (77% to 86%). There were 2 cases of pneumothorax (2.5%), one of which needed intervention with tube thoracostomy.

Conclusions: O-arm CT is an effective, and convenient alternative to other 3-dimensional imaging modalities for intraprocedural confirmation of tool-in-lesion during RAB.

背景:机器人辅助支气管镜检查(RAB)旨在增加难以到达的肺部病变的支气管镜可及性。RAB成功的一个限制是计算机断层扫描(CT)到身体的发散。锥形束CT的实时成像越来越多地用于确认RAB期间病变中的正确导航和工具。O型臂CT是一种三维成像模式,以前没有描述过与RAB一起使用。我们的目的是展示在RAB过程中使用O型臂CT时,工具在病变中的可行性、易用性和高确认率。49%的病例涉及≤2cm的结节。44%的病例没有Bronchus征。中位手术时间为80分钟。每个病例的O型臂CT扫描次数中位数为2次。辐射的中位有效剂量为7.2毫西弗。97%(77/79)的病例证实了工具性病变。在79例病例中,有61至68例(77%至86%)得到了明确诊断。有2例(2.5%)发生了胸腔积液,其中1例需要进行胸腔造口术。结论:在RAB过程中,O型臂CT是一种有效、方便的替代其他三维成像方式的方法,可用于术中确认病变中的工具。
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引用次数: 4
Safety and Feasibility of Photodynamic Therapy for Ablation of Peripheral Lung Tumors. 光动力疗法治疗周围型肺肿瘤的安全性和可行性。
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000889
Sandeep Bansal, Rabih I Bechara, Jiten D Patel, Hiren J Mehta, J Scott Ferguson, Benjamin L Witt, Septimiu D Murgu, Kazuhiro Yasufuku, Roberto F Casal

Background: Newer navigational bronchoscopy technologies render peripheral lung lesions accessible for biopsy and potential treatment. We investigated whether photodynamic therapy (PDT) delivered via navigational bronchoscopy is feasible and safe for ablation of peripheral lung tumors.

Methods: Two studies evaluated PDT in patients with solid peripheral lung tumors followed by clinical follow-up (nonresection study, N=5) or lobectomy (resection study, N=10). Porfimer sodium injection was administered 40 to 50 hours before navigational bronchoscopy. Lesion location was confirmed by radial probe endobronchial ultrasonography. An optical fiber diffuser was placed within or adjacent to the tumor under fluoroscopic guidance; laser light (630 nm wavelength) was applied at 200 J/cm of diffuser length for 500 seconds. Tumor response was assessed by modified Response Evaluation Criteria in Solid Tumors at 3 and 6 months postprocedure (nonresection study) and pathologically (resection study).

Results: There were no deaths, discontinuations for adverse events, or serious or grade ≥3 adverse events related to study treatments. Photosensitivity reactions occurred in 8 of 15 patients: 6 mild, 1 moderate, 1 severe (elevated porphyrins noted in blood after treatment). Among 5 patients with clinical follow-up, 1 had complete response, 3 had stable disease, and 1 had progressive disease at 6 months follow-up. Among 10 patients who underwent lobectomy, 1 had no evidence of tumor at resection (complete response), 3 had 40% to 50% tumor cell necrosis, 2 had 20% to 35%, and 4 had 5% to 10%.

Conclusion: PDT for nonthermal ablation of peripheral lung tumors was feasible and safe in this small study. Further study is warranted to evaluate efficacy and corroborate the safety profile.

背景:较新的导航支气管镜技术使周围肺部病变可以进行活检和潜在的治疗。我们研究了通过导航支气管镜提供的光动力疗法(PDT)对周围肺部肿瘤的消融是否可行和安全。方法:两项研究评估了实体性外周肺肿瘤患者的PDT,随后进行了临床随访(无感染研究,N=5)或肺叶切除术(切除研究,N=10)。波菲莫钠注射液在导航支气管镜检查前40至50小时给药。病变位置通过径向探头支气管内超声检查确认。在荧光镜引导下,将光纤扩散器放置在肿瘤内或肿瘤附近;以200J/cm的漫射器长度施加激光(630nm波长)500秒。在术后3个月和6个月(无感染研究)和病理学(切除研究),采用改良的实体瘤反应评估标准评估肿瘤反应。结果:没有死亡、因不良事件中断或与研究治疗相关的严重或≥3级不良事件。15名患者中有8名出现光敏反应:6名轻度,1名中度,1名重度(治疗后血液中卟啉升高)。5例临床随访患者中,1例完全缓解,3例病情稳定,1例在6个月随访时病情进展。在10例接受肺叶切除术的患者中,1例在切除时没有肿瘤迹象(完全缓解),3例肿瘤细胞坏死率为40%至50%,2例为20%至35%,4例为5%至10%。需要进一步的研究来评估疗效并证实安全性。
{"title":"Safety and Feasibility of Photodynamic Therapy for Ablation of Peripheral Lung Tumors.","authors":"Sandeep Bansal,&nbsp;Rabih I Bechara,&nbsp;Jiten D Patel,&nbsp;Hiren J Mehta,&nbsp;J Scott Ferguson,&nbsp;Benjamin L Witt,&nbsp;Septimiu D Murgu,&nbsp;Kazuhiro Yasufuku,&nbsp;Roberto F Casal","doi":"10.1097/LBR.0000000000000889","DOIUrl":"10.1097/LBR.0000000000000889","url":null,"abstract":"<p><strong>Background: </strong>Newer navigational bronchoscopy technologies render peripheral lung lesions accessible for biopsy and potential treatment. We investigated whether photodynamic therapy (PDT) delivered via navigational bronchoscopy is feasible and safe for ablation of peripheral lung tumors.</p><p><strong>Methods: </strong>Two studies evaluated PDT in patients with solid peripheral lung tumors followed by clinical follow-up (nonresection study, N=5) or lobectomy (resection study, N=10). Porfimer sodium injection was administered 40 to 50 hours before navigational bronchoscopy. Lesion location was confirmed by radial probe endobronchial ultrasonography. An optical fiber diffuser was placed within or adjacent to the tumor under fluoroscopic guidance; laser light (630 nm wavelength) was applied at 200 J/cm of diffuser length for 500 seconds. Tumor response was assessed by modified Response Evaluation Criteria in Solid Tumors at 3 and 6 months postprocedure (nonresection study) and pathologically (resection study).</p><p><strong>Results: </strong>There were no deaths, discontinuations for adverse events, or serious or grade ≥3 adverse events related to study treatments. Photosensitivity reactions occurred in 8 of 15 patients: 6 mild, 1 moderate, 1 severe (elevated porphyrins noted in blood after treatment). Among 5 patients with clinical follow-up, 1 had complete response, 3 had stable disease, and 1 had progressive disease at 6 months follow-up. Among 10 patients who underwent lobectomy, 1 had no evidence of tumor at resection (complete response), 3 had 40% to 50% tumor cell necrosis, 2 had 20% to 35%, and 4 had 5% to 10%.</p><p><strong>Conclusion: </strong>PDT for nonthermal ablation of peripheral lung tumors was feasible and safe in this small study. Further study is warranted to evaluate efficacy and corroborate the safety profile.</p>","PeriodicalId":15268,"journal":{"name":"Journal of Bronchology & Interventional Pulmonology","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/f8/eb/lbr-30-135.PMC10063184.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9241924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Spontaneous Regression of Metastatic Lung Adenocarcinoma Following a Core Biopsy. 核心活检后转移性肺腺癌的自发消退。
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000867
Bilal F Samhouri, Anastasios Dimou, Jennifer M Boland, Eric S Edell
of PPM was reported in 1982 and since then about 60 cases have been reported in the English literature.3,4 The histologic origin of PPM is unclear. It is hypothesized that they either arise from ectopic arachnoid cells, the small meningeal epithelial nodules or subpleural pluripotent cells.5 The disease generally affects patients in fourth to seventh decade of life and is more common in females. Most cases are asymptomatic at presentation, with lesions being found incidentally on chest imaging. In symptomatic cases, chest pain, cough, hemoptysis, and breathlessness are the common presenting features.4 PPM usually presents as a single, peripheral, round or lobulated, noncalcified parenchymal nodule with well circumscribed margins. Few cases of multiple lung nodules mimicking metastatic lung disease have been reported.6 In most cases the bronchi or pleura are not involved. Endobronchial presentation of meningioma is uncommon, and to the best of our knowledge, only one case of endobronchial PPM has been previously reported.7 Our patient had a single large lobulated endobronchial mass which was well circumscribed and appeared to arise from the right upper lobe bronchus. Most cases of PPM are benign, slow growing tumors which have an excellent prognosis with very few cases of metastases or recurrence. Only 3 cases of malignant transformation of PPM have been reported thus far.8 Microscopically, these tumors are composed of spindle-shaped or ovoid cells arranged in lobules or a whorl pattern with psammoma bodies commonly being seen. In our case histopathological examination showed sheets and papillae of uniform cuboidal cells with round nuclei with mild nuclear atypia. Immunohistochemistry staining was positive for vimentin and EMA, characteristic of meningioma. The treatment of choice for pulmonary meningioma has historically been surgical resection. While wedge resection is ideal for benign peripheral lesions, lobectomy is preferred for malignant or central lesions. In view of the benign nature of the disease and low recurrence, we attempted to do a minimally invasive, endobronchial resection. Complete patency of bronchial tree was achieved with complete reexpansion of the collapsed lung postendobronchial resection. To the best of our knowledge this is the first case of endobronchial PPM where bronchoscopic resection was attempted. However, the patient eventually required thoracoscopic bilobectomy as there was a recurrence after 3 months. In conclusion, PPM is a rare disease with endobronchial presentation being reported only 1 case earlier. It should be considered in the differential diagnosis of endobronchial mass lesions and peripheral lung nodules.
{"title":"Spontaneous Regression of Metastatic Lung Adenocarcinoma Following a Core Biopsy.","authors":"Bilal F Samhouri,&nbsp;Anastasios Dimou,&nbsp;Jennifer M Boland,&nbsp;Eric S Edell","doi":"10.1097/LBR.0000000000000867","DOIUrl":"10.1097/LBR.0000000000000867","url":null,"abstract":"of PPM was reported in 1982 and since then about 60 cases have been reported in the English literature.3,4 The histologic origin of PPM is unclear. It is hypothesized that they either arise from ectopic arachnoid cells, the small meningeal epithelial nodules or subpleural pluripotent cells.5 The disease generally affects patients in fourth to seventh decade of life and is more common in females. Most cases are asymptomatic at presentation, with lesions being found incidentally on chest imaging. In symptomatic cases, chest pain, cough, hemoptysis, and breathlessness are the common presenting features.4 PPM usually presents as a single, peripheral, round or lobulated, noncalcified parenchymal nodule with well circumscribed margins. Few cases of multiple lung nodules mimicking metastatic lung disease have been reported.6 In most cases the bronchi or pleura are not involved. Endobronchial presentation of meningioma is uncommon, and to the best of our knowledge, only one case of endobronchial PPM has been previously reported.7 Our patient had a single large lobulated endobronchial mass which was well circumscribed and appeared to arise from the right upper lobe bronchus. Most cases of PPM are benign, slow growing tumors which have an excellent prognosis with very few cases of metastases or recurrence. Only 3 cases of malignant transformation of PPM have been reported thus far.8 Microscopically, these tumors are composed of spindle-shaped or ovoid cells arranged in lobules or a whorl pattern with psammoma bodies commonly being seen. In our case histopathological examination showed sheets and papillae of uniform cuboidal cells with round nuclei with mild nuclear atypia. Immunohistochemistry staining was positive for vimentin and EMA, characteristic of meningioma. The treatment of choice for pulmonary meningioma has historically been surgical resection. While wedge resection is ideal for benign peripheral lesions, lobectomy is preferred for malignant or central lesions. In view of the benign nature of the disease and low recurrence, we attempted to do a minimally invasive, endobronchial resection. Complete patency of bronchial tree was achieved with complete reexpansion of the collapsed lung postendobronchial resection. To the best of our knowledge this is the first case of endobronchial PPM where bronchoscopic resection was attempted. However, the patient eventually required thoracoscopic bilobectomy as there was a recurrence after 3 months. In conclusion, PPM is a rare disease with endobronchial presentation being reported only 1 case earlier. It should be considered in the differential diagnosis of endobronchial mass lesions and peripheral lung nodules.","PeriodicalId":15268,"journal":{"name":"Journal of Bronchology & Interventional Pulmonology","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9327304","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Endobronchial Primary Pulmonary Meningioma: A Rare Cause of Right Main Bronchus Obstruction. 支气管内原发性肺脑膜瘤:一种罕见的右主支气管阻塞原因。
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000866
Virender P Prasad, Naseer Mohammed Abdul, Srikanth Peddi, Chetan R Vaddepally, Dommata Raghotham Reddy, Venkata N Maturu
{"title":"Endobronchial Primary Pulmonary Meningioma: A Rare Cause of Right Main Bronchus Obstruction.","authors":"Virender P Prasad,&nbsp;Naseer Mohammed Abdul,&nbsp;Srikanth Peddi,&nbsp;Chetan R Vaddepally,&nbsp;Dommata Raghotham Reddy,&nbsp;Venkata N Maturu","doi":"10.1097/LBR.0000000000000866","DOIUrl":"10.1097/LBR.0000000000000866","url":null,"abstract":"","PeriodicalId":15268,"journal":{"name":"Journal of Bronchology & Interventional Pulmonology","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9327309","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Value of Thoracic Ultrasonography in a Case of Tension Hydrothorax. 胸部超声在1例张力性胸腔积液中的价值。
IF 3.3 Q2 Medicine Pub Date : 2023-04-01 DOI: 10.1097/LBR.0000000000000856
Maxwell Diddams, Shalini Mehta, Christina R MacRosty
CASE We present a 79-year-old female with history of hypertension, stage III chronic kidney disease, and supraventricular tachycardia managed with metoprolol succinate, who presented to the emergency department through ambulance after a fall when standing from a seated position. Triage vital signs were notable for blood pressure 81/49, heart rate 93, oxygen saturation 95% on 3L nasal cannula. Blood pressure did not improve after 3L of intravenous crystalloid. Physical exam revealed a cachectic woman in moderate respiratory distress with absent breath sounds on the right. Electrocardiography revealed sinus tachycardia at a rate of 108, premature atrial contractions, and no atrioventricular blocks. Labs notable for white blood cells of 13.8×103/μL, hemoglobin 10.9 g/dL. Chemistries notable for sodium 134mEq/L, creatinine 1.89mg/dL, blood urea nitrogen 62mg/dL. Troponin was elevated to 0.053 ng/ mL. Lactate was 3.5mmol/L and improved after intravenous fluids. Chest radiography revealed complete opacification of the right hemithorax with tracheal deviation to the left (Fig. 1, panel A) and noncontrasted computed tomography (CT) scan of the chest revealed a large right upper lobe mass and a heterogeneous cystic mass-like lesion occupying the right hemithorax with small pleural effusion (Fig. 1, panel C). Bedside thoracic ultrasonography showed a large heterogenous, loculated pleural effusion with solid structures and an inverted right hemidiaphragm (Fig. 1, Panel E and F). Bedside echocardiography showed a leftward-deviated heart without evidence of pericardial effusion. The inferior vena cava was >2.1 cm in diameter without respiratory variation. A 14 French pigtail chest tube was placed with a forceful gush of fluid on entering the pleural space and immediate drainage of 2000mL serosanguinous fluid. The patient’s blood pressure improved to 122/65 within 3 minutes of chest tube placement. Pleural fluid studies were consistent with a neutrophilic exudate with 79% neutrophils, lactate dehydrogenase 14,892U/L, protein 7.9 g/dL, glucose 23mg/dL, albumin 4.4 g/dL, and hematocrit 7 (Table 1). Cytology was negative for malignant cells. Postprocedure contrasted CT scan demonstrated persistent effusion, multiple masses involving the hilum, persistently collapsed right lung, and improvement in mediastinal shift (Panel D). Positron emission tomography 5 days later revealed a hypermetabolic right upper lobe paramediastinal mass with invasion into the right medial pericardium and the right parietal pleura, likely a primary lung cancer. Because of her advanced disease at presentation and comorbidities, the patient declined biopsy for diagnosis and elected to pursue comfort measures only. She did not want any further procedures so the chest tube remained in place until death. DISCUSSION Tension hydrothorax is a lifethreatening extreme of pleural effusion that threatens cardiopulmonary collapse.1–8 Because of its rarity, the exact physiology is imperfectly described
{"title":"The Value of Thoracic Ultrasonography in a Case of Tension Hydrothorax.","authors":"Maxwell Diddams,&nbsp;Shalini Mehta,&nbsp;Christina R MacRosty","doi":"10.1097/LBR.0000000000000856","DOIUrl":"10.1097/LBR.0000000000000856","url":null,"abstract":"CASE We present a 79-year-old female with history of hypertension, stage III chronic kidney disease, and supraventricular tachycardia managed with metoprolol succinate, who presented to the emergency department through ambulance after a fall when standing from a seated position. Triage vital signs were notable for blood pressure 81/49, heart rate 93, oxygen saturation 95% on 3L nasal cannula. Blood pressure did not improve after 3L of intravenous crystalloid. Physical exam revealed a cachectic woman in moderate respiratory distress with absent breath sounds on the right. Electrocardiography revealed sinus tachycardia at a rate of 108, premature atrial contractions, and no atrioventricular blocks. Labs notable for white blood cells of 13.8×103/μL, hemoglobin 10.9 g/dL. Chemistries notable for sodium 134mEq/L, creatinine 1.89mg/dL, blood urea nitrogen 62mg/dL. Troponin was elevated to 0.053 ng/ mL. Lactate was 3.5mmol/L and improved after intravenous fluids. Chest radiography revealed complete opacification of the right hemithorax with tracheal deviation to the left (Fig. 1, panel A) and noncontrasted computed tomography (CT) scan of the chest revealed a large right upper lobe mass and a heterogeneous cystic mass-like lesion occupying the right hemithorax with small pleural effusion (Fig. 1, panel C). Bedside thoracic ultrasonography showed a large heterogenous, loculated pleural effusion with solid structures and an inverted right hemidiaphragm (Fig. 1, Panel E and F). Bedside echocardiography showed a leftward-deviated heart without evidence of pericardial effusion. The inferior vena cava was >2.1 cm in diameter without respiratory variation. A 14 French pigtail chest tube was placed with a forceful gush of fluid on entering the pleural space and immediate drainage of 2000mL serosanguinous fluid. The patient’s blood pressure improved to 122/65 within 3 minutes of chest tube placement. Pleural fluid studies were consistent with a neutrophilic exudate with 79% neutrophils, lactate dehydrogenase 14,892U/L, protein 7.9 g/dL, glucose 23mg/dL, albumin 4.4 g/dL, and hematocrit 7 (Table 1). Cytology was negative for malignant cells. Postprocedure contrasted CT scan demonstrated persistent effusion, multiple masses involving the hilum, persistently collapsed right lung, and improvement in mediastinal shift (Panel D). Positron emission tomography 5 days later revealed a hypermetabolic right upper lobe paramediastinal mass with invasion into the right medial pericardium and the right parietal pleura, likely a primary lung cancer. Because of her advanced disease at presentation and comorbidities, the patient declined biopsy for diagnosis and elected to pursue comfort measures only. She did not want any further procedures so the chest tube remained in place until death. DISCUSSION Tension hydrothorax is a lifethreatening extreme of pleural effusion that threatens cardiopulmonary collapse.1–8 Because of its rarity, the exact physiology is imperfectly described","PeriodicalId":15268,"journal":{"name":"Journal of Bronchology & Interventional Pulmonology","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9328624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Bronchology & Interventional Pulmonology
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