Literature DB >> 35184743

Percutaneous intravenous catheter forceps biopsy in right atrial mass: two case reports and literature review.

Lei Chang1, Chenyi Gong2, Haitao Lu3, Yihai Liu1, Lina Kang2, Jianzhou Chen2, Lian Wang4,5, Biao Xu6,7.   

Abstract

BACKGROUND: Primary malignant tumors of the heart are rare. Although preoperative histological diagnosis is difficult, it has paramount value in therapeutic strategy development and prognostic estimation. Herein, we reported 2 cases of intracardiac tumors. CASES
PRESENTATION: Both patients presented to the hospital with heart-related symptoms. Echocardiography showed massive masses in the atrium and positron emission tomography-computed tomography (PET/CT) revealed hypermetabolism and invasiveness. One patient cannot take surgery due to extensive metastasis and poor condition. The other patient was primarily diagnosed with lymphoma, and surgery was not recommended. They successfully underwent intravenous atrial biopsy, and histological samples confirmed intimal sarcoma and diffuse large B cell lymphoma. Based on immunohistochemical and molecular assessments, targeted chemotherapy was administered, resulting in clinical and imaging remission at discharge.
CONCLUSIONS: Percutaneous intravenous catheter biopsy as a safe invasive test provides an accurate pathological diagnosis after imaging evaluation, and offers a therapeutic direction. Nonmalignant masses and some chemo-radiosensitive malignant tumors in the atrium could have good prognosis after targeted therapy.
© 2022. The Author(s).

Entities:  

Keywords:  Cardiac lymphoma; Cardiac sarcoma; Case report; Intimal sarcoma; Intravenous biopsy

Mesh:

Year:  2022        PMID: 35184743      PMCID: PMC8859873          DOI: 10.1186/s12872-022-02507-x

Source DB:  PubMed          Journal:  BMC Cardiovasc Disord        ISSN: 1471-2261            Impact factor:   2.298


Background

Primary cardiac tumors (PCTs) are extremely rare, with an autopsy incidence ranging from 0.001 to 0.030% [1]. A 14-year population-based study revealed a prevalence for PCT of 1.38/100,000 [2]. A meta-analysis showed that the pooled prevalence of malignancies among patients diagnosed with PCT is 9.9% [3]. Primary cardiac malignancies (PCMs) still have poor prognosis, and attempts to overcome diagnostic and therapeutic difficulties are needed. The majority of PCMs are sarcomas, including angiosarcoma, rhabdomyosarcoma, fibrosarcoma, and Kaposi sarcoma. Mesotheliomas and primary cardiac lymphomas are the next most common primary cardiac malignancies [4]. Intimal sarcoma, a mesenchymal tumor, is the least reported primary cardiac tumor that originates from the tunica intima of large blood vessels, and rarely involves the heart [5]. PCT has multiple clinical presentations, ranging from asymptomatic detection in imaging tests to palpitation, shortness of breath, emaciation and even aborted sudden cardiac death [6]. Preoperative histological diagnosis is difficult but has paramount value in therapeutic strategy development and prognostic estimation. Herein, we successfully performed percutaneous atrial mass biopsy (PAMB), and established histological diagnosis instead of surgery. Safety, procedure and benefit for patients are key points for the extensive use of this invasive diagnostic technique.

Cases presentation

Case 1: A 48-year-old male was presented with palpitation and chest distress after activity for 3 months. Echocardiography revealed a large mass (maximum size: 58 mm × 40 mm) attached to the lateral and posterior atrial walls, invading the inferior vena cava. Cardiac magnetic resonance (CMR) imaging showed right atrial soft tissue mass close to the tricuspid orifice with the valve leaflet (Fig. 1a). Positron emission tomography-computed tomography (PET/CT) suggested enhanced fluorodeoxyglucose (FDG) metabolism signals in the right atrium, pericardium, mediastinum lymph nodes, and left lung nodules (Fig. 1b, c). Surgical resection was not recommended because of extensive metastasis. Totally 2 months later, the patient experienced severe chest tightness, wheezing, sitting breathing, lower limb edema, and bilateral bloody pleural effusion. Radiographic evaluations showed a right atrial mass and multiple metastatic lesions that had progressed (Fig. 2a–d).
Fig. 1

CMR shows the right atrium soft tissue mass closed to the tricuspid orifice (a). PET/CT scan suggests intensive tracer uptake of the right atrial mass, pericardium, lung and mediastinal lymph nodes (b, c)

Fig. 2

CT imaging displayed right atrium mass (a) and suspected metastases in liver (b). Scan enhancement CT scan show abnormal signals in the right atrium, pericardium (c), and liver (d) in 2 months. After 5 cycles of comprehensive immune anti-tumor therapy, significant reduction is detected in the right atrial intimal sarcoma (e) and liver mass (f) dimension

CMR shows the right atrium soft tissue mass closed to the tricuspid orifice (a). PET/CT scan suggests intensive tracer uptake of the right atrial mass, pericardium, lung and mediastinal lymph nodes (b, c) CT imaging displayed right atrium mass (a) and suspected metastases in liver (b). Scan enhancement CT scan show abnormal signals in the right atrium, pericardium (c), and liver (d) in 2 months. After 5 cycles of comprehensive immune anti-tumor therapy, significant reduction is detected in the right atrial intimal sarcoma (e) and liver mass (f) dimension To confirm the nature of the mass, PAMB was performed through the femoral vein, wherein three tissues were removed. The pathological analysis revealed thrombus which was consistent with imaging features. We speculated that blood flow changes caused blood turbulence. This could increase the risk of thrombus adhesion on the mass surface and influence biopsy results. After 3 weeks, the patient underwent second PAMB through the internal jugular vein. With the bedside echocardiography auxiliary positioning, three tumor tissues were removed from the atrial mass. The pathological report concluded intraepithelial metaplasia; the abnormal cell pattern showed high-grade spindle cell neoplasm with moderate atypia and focal necrosis, consistent with intimal sarcoma histologically (Fig. 3c, d). The patient was finally diagnosed with primary cardiovascular intimal sarcoma (stage IV).
Fig. 3

The pathology of the first biopsy via femoral vein shows a large amount of cellulose and blood cells, diagnosed as thrombus (a hematoxylin and eosin, 40 × 10). The pathology of the secondary biopsy through the right internal jugular vein reveals a spindle cell tumor, some areas are rich in spindle cells, with moderate atypia and focal necrosis, and the histology is consistent with intimal sarcoma (b hematoxylin and eosin, 40 × 10). Immunohistochemistry-positive neoplastic cells for PRAME (c 40 × 10)

The pathology of the first biopsy via femoral vein shows a large amount of cellulose and blood cells, diagnosed as thrombus (a hematoxylin and eosin, 40 × 10). The pathology of the secondary biopsy through the right internal jugular vein reveals a spindle cell tumor, some areas are rich in spindle cells, with moderate atypia and focal necrosis, and the histology is consistent with intimal sarcoma (b hematoxylin and eosin, 40 × 10). Immunohistochemistry-positive neoplastic cells for PRAME (c 40 × 10) Subsequently, he underwent exploratory tumor immunotherapy. The primary drug was the immune checkpoint inhibitor PD-1 antibody, which could activate endogenous anti-tumor response and has confirmed efficacy in some soft-tissue sarcomas [7]. After five cycles, the patient’s symptoms were relieved, and cardiac function was improved significantly. Re-examination by chest CT revealed a shrunk tumor in the right atrium, and the number of metastases was decreased substantially (Fig. 2e, f). At the time of drafting this manuscript, the condition of patient was stable and receiving the thirteenth cycle of immunotherapy. His health condition and life quality were improved significantly. Case 2: A 77-year-old woman presented to our hospital with a half-month history of chest tightness and dyspnea. Sinus tachycardia and pulmonary moist rales were found on physical examination. Transthoracic echocardiography revealed an intracardiac mass (maximum size: 49 mm × 38 mm) attached to the left atrium that invaded the right atrial walls and tricuspid annulus. The atrial mass protruding into the pericardial cavity caused moderate pericardial effusion and early signs of tamponade. CMR confirmed the presence of an invasive intracardiac mass (Fig. 4a, b) and PET-CT scan revealed high FDG uptake in the neoplasm and mediastinum lymph nodes (Fig. 4c). The patient underwent pericardium puncture drainage, and abnormal lymphocytes were found by pericardial effusion smear examination. Abnormally increased percent of heteromorphic monoclonal B lymphocytes was detected by flow cytometry. Given the right atrium invasion of the mass, and our successful experience of PAMB in the right atrium, we performed percutaneous jugular puncture and catheterization, and subsequent atrium angiography revealed a filling defect in the right atrium. Then, biopsy catheter was positioned at the neoplasm, and TTE provided multiple heart sections that confirmed the relative positions of biopsy forceps, atrial walls, and the mass. We successfully obtained 2 tissue pieces to avoid thoracotomy, without complication.
Fig. 4

CMR confirmed left atrial mass invaded right atrium (a, b) and PET-CT scan revealed high FDG uptake in atrum and mediastinal lymph nodes (c)

CMR confirmed left atrial mass invaded right atrium (a, b) and PET-CT scan revealed high FDG uptake in atrum and mediastinal lymph nodes (c) Immunohistochemical analysis of the specimen showed that the obtained tumor cells were positive for CD20, MUM1, CD5, and Bcl-2; negative for CD3, CD99, CD10 and CD30; and equivocalfor Bcl-6. Ki67, Bcl-2, and c-MYC labeling indexes were all 90% (Fig. 5a–d). However, bone marrow biopsy showed no infiltration of abnormal lymphocytes. Then, the patient was diagnosed with cardiac diffuse large B cell lymphoma, of non-germinal center B-cell-like type. After 3 cycles of chemotherapy with R-miniCHOP (rituximab, cyclophosphamide, adriamycin, vincristine, and prednisone), the clinical symptoms were improved remarkably. Repeated echocardiography demonstrated disappearance of the intracardiac mass. PET/CT showed no area of FDG hypermetabolism in the heart or intrathoracic lymph nodes. The patient would accept the full course of treatment with continuous follow-up.
Fig. 5

The histopathological section shows diffuse growth of large lymphocytes with a small amount of apoptotic necrosis (a hematoxylin and eosin, 40 × 10). Immunohistochemistry-positive neoplastic lymphoid cells for CD20 (b 40 × 10), CD5 (c × 400) and Bcl2 (d 40 × 10)

The histopathological section shows diffuse growth of large lymphocytes with a small amount of apoptotic necrosis (a hematoxylin and eosin, 40 × 10). Immunohistochemistry-positive neoplastic lymphoid cells for CD20 (b 40 × 10), CD5 (c × 400) and Bcl2 (d 40 × 10)

Discussion and conclusions

A recent multicenter analysis showed that PCM mainly affected adults (mean age of 53 years), and had a dismal long-term survival rate despite various modes of treatment [8]. The overall 1-year and 5-year survival rates were 45.3% and 11.5% in the latter study. Patients who underwent surgery had significantly better survival compared with those administered the non-surgical treatment. Moeri-Schimmel et al. indicated that most PCM patients who received postoperative radiotherapy had longer survival time than those who undergo only surgery [9]. Multi-institutional data from the National Cancer Database also confirmed that stage III PCM patients who undergo surgery and receive perioperative chemotherapy have better survival compared with those who did not receive this treatment [8]. Although surgical resection remains the first treatment choice for cardiac sarcoma [1], radiotherapy and chemotherapy are increasingly important. Thus, individualized radiotherapy and chemotherapy should be recommended in inoperable patients. A prospective study of right-sided tumors showed that neoadjuvant chemotherapy reduces the tumor burden, improving resectability and survival in complex cardiac tumors [10]. Although intracardiac mass is considered as a dangerous signal of PCM, it should be noticed that a neoplasm located in the atrium usually causes less systolic dysfunction and ventricular arrhythmia. Moreover, benign lesions such as thrombus and myxoma, accounting for a large proportion of atrial masses, but seldom appear in ventricles. Therefore, the criticality of atrial mass is different from that of ventricular mass. For atrial mass, more effort is needed to enable precise diagnosis, especially histological diagnosis. Echocardiography, CT, CMR, and PET/CT imaging could help in the preliminary differentiation between malignant and benign tumors based on tumor shape, aggressiveness, and radioactive material intake [11, 12]. However, several intra-atrial PCMs firstly misdiagnosed as benign tumors or incompletely resected may relapse in a short time [13]. Generally, histological diagnosis before tumor therapy could avoid this situation and help differentiate primary sarcomas from other malignancies (such as lymphomas that do not require surgery). After that, the patients could be administered the best-personalized multimodality treatment [14]. In patients with potential resectable cardiac sarcomas but limited by poor cardiac and pulmonary functions [15], pathological results could facilitate neoadjuvant chemotherapy to improve the basic condition of patients and create opportunities or strengthen the effect of surgical resection. The endomyocardial biopsy technology has been widely used in cardiomyopathy, and has been extended to ventricle mass biopsy. By contrast, atrial biopsy has not been promoted for some reason. Atrial biopsy means thinner cardiac muscle walls, closer intervention to the relatively fragile vein, and higher risk of thrombus detachment. In 1989, Gosalakkal and Sugrue [16] firstly reported atrium biopsy and removed the tumor tissue from the cardiac chamber. To further evaluate the safety and efficacy of percutaneous atrial mass biopsy, we analyzed 51 cases in 47 articles and our 2 PAMB cases (Table 1). Most patients had undergone simple right atrial lump biopsy, while 3 cases underwent transseptal left atrial biopsy. Of all cases, only 1 patient reported potential complications post-biopsy [17]. The latter patient developed severe hypotensive shock after the procedure. After fluid resuscitation and treatment with vasoactive agents, the shock symptoms were stabilized. Since no obvious signs of perforation and rupture of the atrium or inferior vena cava were noted, mechanical damage to the heart caused by biopsy was not considered.
Table1

Atrial mass cases diagnosed by intravenous biopsy

AgeSexBiopsy locationTransvenous pathwayGuidance MethodPresenting reasonsPathological diagnosisTreatmentOutcomePMID
14MaleRAFemoral veinDSA + TEEChest pain, cough, and hemoptysis///2,334,836 [18]
46FemaleRAJugular veinDSASymptoms of Upper respiratory infectionMetastases of melanoma//2,765,329 [16]
83FemaleRAFemoral veinDSADyspnea and hypodynamiaPapillary fibroelastomaSymptomatic treatment/2,816,690 [19]
69FemaleRAFemoral veinDSA + TEEDyspnea, edema, and syncopeThrombusSurgical resectionRemission7,499,910 [20]
52FemaleRAFemoral veinDSA + TEEHistory of cirrhosisMetastases of liver cancer/Deceased8,131,572 [21]
69MaleRAFemoral veinDSA + TEEDyspnea, cough, and hemoptysisMetastases of melanoma//8,154,436 [22]
69FemaleRAJugular veinDSA + TEEDyspnea, dehydration, and ventricular tachycardiaThrombusSymptomatic treatment/8,365,328 [23]
62MaleRAJugular veinDSA + TEEEdema and hepatic encephalopathyMetastatic adenocarcinoma/Deceased8,498,328 [24]
73FemaleRAJugular veinDSA + TEEEdema, cough, fever, and dyspneaLymphomaChemotherapyRemission8,579,042 [25]
69MaleRAFemoral veinDSA + ICEFlu symptomsMetastasis of lung cancer//8,611,294 [26]
73MaleRAJugular veinDSA + TEEAsymptomaticMetastases of melanomaChemotherapy/8,945,488 [27]
35MaleRAFemoral veinDSA + TEEDyspnea and coughAngiosarcomaChemotherapyRemission8,974,823 [28]
//RAJugular veinDSA + TEE/Angiosarcoma//9,070,559 [29]
62MaleRAJugular veinDSA + TEEDyspnea, chest pain andUndifferentiated sarcomaChemotherapyDeceased9,339,428 [30]
66/RA + ASFemoral veinDSA + TEEMyocardial infarctionLymphomaChemotherapy/9,454,452 [31]
64FemaleRA/DSA + TEEDizzinessLymphoma//9,487,479 [32]
47MaleRAJugular veinDSA + TTEDyspnea, edema and pleural effusionLymphomaChemotherapy/9,829,904 [33]
50MaleRA/DSA + TEEOrthopnea, fever, and pleural effusionThrombusSurgical resectionDeceased9,932,633 [34]
39Female////Myxoma//10,231,677 [35]
//RA//////10,763,354 [36]
77FemaleRA/DSA + TEEDyspnea, edema and hypodynamiaLymphomaChemoradiotherapyRemission10,790,358 [37]
75MaleRAFemoral veinDSA + TEEHemoptysisLymphomaChemotherapyRemission10,842,397 [38]
79FemaleRAFemoral veinDSA + ICEDyspnea and edemaNeuroblastoma//10,952,166 [39]
//LA/DSA + TEE/Atrial sarcoma//11,223,492 [40]
52MaleRAJugular veinDSA + TEEEpigastric acheAngiosarcomaChemotherapyRemission12,019,433 [41]
62MaleRAFemoral veinDSA + TEEDyspnea and dizzinessLymphomaChemotherapyRemission12,848,708 [42]
64MaleRAJugular veinDSA + TEEHeart failureLymphomaChemotherapyRemission14,622,547 [43]
52MaleRAJugular veinDSA + TEEDyspnea, chest pain, and edemaMetastases of liver cancerSymptomatic treatmentDeceased15,546,373 [44]
63FemaleRAJugular veinDSA + ICEDyspnea and centrum fractureLipomyomaExpectant treatment/16,880,106 [45]
61MaleRASubclavian vein for biopsy, femoral vein for ICEDSA + ICEVentricular tachycardiaLymphoma//17,015,040 [46]
38MaleRA/DSA + TTEDyspneaLymphomaChemotherapyRemission17,383,751 [47]
52MaleRAFemoral veinDSA + ICECardiac tamponadeGranulocytic sarcomaChemoradiotherapy and hematopoietic stem cell transplantationRemission18,498,027 [48]
56Female///Repeated pericardial effusion///18,805,775 [49]
67FemaleRAJugular vein for biopsy, femoral vein for ICEDSA + ICEThe discomfort of the precordial areaParagangliomasSurgical resection/18,818,096 [17]
47FemaleRAJugular vein for biopsy, femoral vein for ICEDSA + ICEHypodynamia and atrial fibrillationParagangliomasSurgical resection/18,818,096 [17]
30MaleRA/IVCJugular vein for biopsy, femoral vein for ICEDSA + ICEPolyserositis and edema after heart transplantBacterial emboliSurgical resectionRemission18,818,096 [17]
70MaleRA/IVC//Ascites after heart transplantationCardiac amyloidosisSymptomatic treatmentDeceased18,818,096 [17]
63FemaleRAJugular vein for biopsy, femoral vein for ICEDSA + ICEChest discomfort and edemaLymphomaChemotherapyRemission19,057,087 [50]
59MaleRA/DSA + TEEDyspnea, cough, chest discomfort, fever and hypodynamiaLymphomaChemotherapyRemission19,142,595 [51]
64FemaleRA/DSA + TTEDizziness and history of endometrial carcinomaMetastases of endometrial adenocarcinoma/20,027,104 [52]
22FemaleRA/DSA + ICEDyspnea and syncopeAngiosarcomaChemotherapy/20,585,357 [53]
57FemaleRA/DSA + TEEDyspnea and back painIntimal sarcomaChemotherapyRemission20,966,612 [54]
44MaleRAJugular vein for biopsy, femoral vein for ICEDSA + ICEDyspneaLymphomaChemotherapyRemission22,576,384 [55]
31MaleLA/DSA + TEEDyspnea and hypodynamiaPoorly differentiated sarcomaChemotherapyDeceased23,109,774 [56]
46MaleRAFemoral veinDSA + ICEHistory of myxomaMyxomaExpectant treatmentRemission25,240,574 [57]
53MaleRARight femoral vein for biopsy, left femoral vein for ICEDSA + ICEDyspnea and weight lossMetastases of lung cancerChemotherapyDeceased25,810,740 [58]
51FemaleRA/DSA + ICEDyspnea and edemaAngiosarcomaChemotherapyDeceased25,810,740 [58]
47FemaleRAFemoral veinDSA + ICENeoadjuvant chemotherapy for breast cancerThrombusSurgical resectionRemission27,068,834 [59]
59MaleLA/DSA + TEEFever, weight loss, and history of HIV infectionLymphomaChemotherapyRemission31,020,117 [60]
61MaleRA/DSA + ICEJaundice, hypodynamia and diagnosed as IgG4/related diseaseIgG4/related diseaseHormonotherapyRemission31,118,383 [61]
47FemaleRAJugular vein for biopsy, femoral vein for ICEDSA + ICECough and pulmonary nodulesAngiosarcomaChemotherapyRemission32,874,873 [62]
48MaleRAFemoral vein and jugular veinDSA + TTEPalpitation and chest discomfortIntimal sarcomaChemotherapyRemissionPresent case
77FemaleRAJugular veinDSA + TTEDyspnea and chest discomfortLymphomaChemotherapyRemissionPresent case
Atrial mass cases diagnosed by intravenous biopsy Among 37 cases with reported malignant tumors, lymphomas accounted for the largest proportion (15/37), followed by soft tissue sarcomas (13/37), and 9/37 reported metastatic tumors. Table 2 shows their prognoses differed from mass location and pathological results. In all patients, atrial lymphoma patients had the best prognosis, including 11 patients who presented clinical remission or even cured after receiving corresponding chemotherapy; the prognoses of another 4 lymphoma patients were not reported. Most atrial soft-tissue sarcoma patients cannot tolerate surgery and radiotherapy due to heart-related symptoms; 6 patients achieved clinical remission and 3 had tumor exacerbation in short-term visits. Of another 4 patients diagnosed with atrial thrombosis, 2 had satisfactory prognosis, and 1 diagnosed with angiosarcoma by subsequent surgical specimens died of tumor recurrence and metastasis [34]. In addition, a patient pathologically diagnosed with an IgG4-related disease received hormone therapy and showed good prognosis [61].
Table 2

Prognosis of patients differs with respect to the mass locations and the pathological results

Neoplasm location and pathologyOverall responseProgressive diseaseNot mentionedTotal
All cases2292253
First attack symptom
 Related to the mass1781338
 Unrelated to the mass51410
 No discomfort or not mentioned0055
Biopsy location
 Right atrium or atrial septum2182150
 Involved left atrium1113
Malignant tumor
 Lymphoma110415
 Metastatic tumor0459
 Soft-tissue sarcoma63413
Benign tumor
 Lipomyoma0011
 Myxoma1012
 Paraganglioma0022
 Fibroma0011
Others
 Thrombus2114
 Bacterial vegetation1001
 IgG4-related diseases1001
 Myocardial amyloidosis0101
 Not mentioned0033

The overall response means patients’ clinical symptoms were relieved and/or healed, or the tumor volume was reduced. Progressive disease means patients could not benefit from the treatment, it was worsened, or led to death

Prognosis of patients differs with respect to the mass locations and the pathological results The overall response means patients’ clinical symptoms were relieved and/or healed, or the tumor volume was reduced. Progressive disease means patients could not benefit from the treatment, it was worsened, or led to death For various spatial atrial mass locations, different vessel approaches and ultrasonic guidance methods could be selected in PAMB. Biopsy has been performed via the internal jugular, femoral and subclavian veins. Transesophageal echocardiography (TEE) is highly effective in mass locating and bioptome guidance. Hence, about 50% of physicians use TEE as a supplementary tool to digital subtraction angiography (DSA). Transthoracic echocardiography (TTE) is more convenient but provides less location information compared with TEE, thereby necessitating highly experienced doctors. Intracardiac echocardiography (ICE) can provide the most precise intra-atrial imaging and structures, but requires an extra-intravenous ultrasound catheter, which limits its application; only about 33% of physicians utilize this method. Table 3 shows the proportion of different guiding methods in all transvenous atrium biopsy cases.
Table 3

Proportion of different guiding methods in all transvenous atrium biopsy cases

Reported imaging and guidance methodNot mentioned
DSA onlyTTE + DSATEE + DSAICE + DSA
Number of cases2624174
Proportion4.1%12.2%49.0%34.7%
Proportion of different guiding methods in all transvenous atrium biopsy cases Percutaneous intravenous catheter biopsy provided accurate pathological diagnosis after imaging evaluation, avoiding unnecessary surgical excision and reducing medical resource waste. Benign tumors, thrombus, bacterial vegetation, and lymphoma detected by PAMB could be cured. Nevertheless, when pathological biopsy results suggest thrombus but do not correspond to clinical symptoms, doctors should consider the possibility of false negatives. Multiple biopsies from different vessel approaches and varied mass locations might reduce the probability of misleading results. However, whether biopsies are beneficial to PCM patients is currently controversial. Ryo et al. [34] speculated that intravenous cardiac biopsy and subsequent chemotherapy is not beneficial to cardiac sarcoma patients. The core challenge is the effectiveness of subsequent anti-tumor therapy. Significantly, with the development of anti-tumor therapy, appropriate treatments have proved effective. PAMB as a safe, effective, and minimally invasive procedure for histological diagnosis before surgical resection would be applied increased comprehensively.
  57 in total

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Review 4.  CT and MR imaging of primary cardiac malignancies.

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Journal:  Curr Treat Options Oncol       Date:  2019-06-27

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Journal:  Future Cardiol       Date:  2015-08-03

Review 7.  Prevalence of primary cardiac tumor malignancies in retrospective studies over six decades: a systematic review and meta-analysis.

Authors:  Shuai He; Yide Cao; Wei Qin; Wen Chen; Li Yin; Hao Chai; Zhonghao Tao; Shaowen Tang; Zhibing Qiu; Xin Chen
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9.  PD1/PD-L1 targeting in advanced soft-tissue sarcomas: a pooled analysis of phase II trials.

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10.  Primary intimal (spindle cell) sarcoma of the heart: a case report and review of the literature.

Authors:  A Ibrahim; A Luk; P Singhal; Bo Wan; A Zavodni; R J Cusimano; J Butany
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