scholarly journals Prostate Cancer-Associated Trousseau´S Syndrome Versus Asymptomatic Isolated Muscular Calf Vein Thrombosis as the Origin of Acute Submassive Pulmonary Embolism: A Case Report and Review of the Literature

2020 ◽  
pp. 1-6
Author(s):  
Antonis Tsamaloukas ◽  
Antonis Tsamaloukas ◽  
Aristoteles Giagounidis ◽  
Jan Roigas ◽  
Stefan Glück

Venous thromboembolism (VTE) is a major cause of morbidity and mortality in cancer patients. Cancer patients have a four to sevenfold increased risk of VTE compared with non-cancer patients and approximately 20% -30% of all VTE occurs in patients with cancer. Incidence of VTE varies with cancer type and is the highest among patients with metastatic-stage disease. Assessing risk of VTE in the patients with cancer and risk stratification tools as the Khorana score may predict VTE. The highest risk is associated with cancers of the pancreas, stomach, brain, and lung and some hematologic malignancies, whereas lower risks are associated with breast and prostate cancer. The incidence rate ratio (IRR) for prostate cancer is 3.25(2,56 - 4,13) and for pancreas 15.56 (10.50-23.0). We give a case report with a quite perplexing undertaking, where a submassive acute pulmonary embolism (PE) originated from an asymptomatic calf vein thrombosis or intertwined with the Trousseau´s syndrome. Essential Section: One of the authors (A.T) was unexpected faced with the diagnosis of poorly differentiated prostate cancer. There were no signs of the disease, the PSA level was normal. As a retired medical oncologist, he had to care for many patients with prostate cancer and had now to cope with this cancer. To make the matter worse he suffered after the radical prostatectomy a submassive asymptomatic pulmonary embolism. Clinically there were no signs if a deep venous thrombosis. The coincidence of both events without clinical signs of a thrombosis could be caused by the Trousseau´s syndrome. Prostasomes extracellular vesicles synthesizes by prostate cancer cells and secreted into body fluids are prothrombotic by virtue of the expression of polyphosphate-activated coagulation factor XII.

2020 ◽  
Vol 26 (7) ◽  
pp. 1769-1773
Author(s):  
Kylee E White ◽  
Christopher T Elder

Introduction As a single agent, fluorouracil has been documented to have a small but present chance of causing extravasation of the port when not properly administered. It has also been shown that cancer patients receiving chemotherapy are at increased risk of deep vein thrombosis, symptomatic or silent. Case report A 43-year-old male patient with stage III colon cancer receiving FOLFOX developed a saddle pulmonary embolism involving possible extravasation that was discovered following cycle 3 of chemotherapy. CT scan and lower extremity Doppler confirmed non-occlusive deep vein thrombosis along with saddle pulmonary embolism. Management and outcome: For acute management, patient underwent bilateral pulmonary artery thrombolysis. Following this, the patient was initiated on rivaroxaban indefinitely. The right subclavian port was removed, and a new port was placed in the left subclavian. Patient went on to receive three more cycles of chemotherapy. Discussion Fluorouracil, an inflammitant, has been shown to have damaging potential, especially in terms of the integrity of the endothelium. Over time, this can lead to serious complications such as cardiotoxicity, including deep vein thrombosis formation. Based on how and when the thrombi were discovered, it is not possible to deduce whether the port, the 5-FU, extravasation or other factors were the precipitators of the formation of the thrombi. The combination of chemotherapy treatment along with CVC placement appears to have an additive risk to the formation of a thrombus. Practitioners should take caution when evaluating for extravasation and CVC integrity and note other potential differentials for causes, including deep vein thrombosis/saddle pulmonary embolism formation.


2020 ◽  
Vol 9 (11) ◽  
pp. 3642
Author(s):  
Valentina Milazzo ◽  
Nicola Cosentino ◽  
Jeness Campodonico ◽  
Claudia Lucci ◽  
Daniela Cardinale ◽  
...  

Patients with cancer are at increased risk of cardiovascular disease, with a reported prevalence of acute coronary syndrome (ACS) ranging from 3% to 17%. The increased risk of ACS in these patients seems to be due to the complex interaction of shared cardiovascular risk factors, cancer type and stage, and chemotherapeutic and radiotherapy regimens. The management of ACS in patients with cancer is a clinical challenge, particularly due to cancer’s unique pathophysiology, which makes it difficult to balance thrombotic and bleeding risks in this specific patient population. In addition, patients with cancer have largely been excluded from ACS trials. Hence, an evidence-based treatment for ACS in this group of patients is unknown and only a limited proportion of them is treated with antiplatelets or invasive revascularization, despite initial reports suggesting their beneficial prognostic effects in cancer patients. Finally, cancer patients experiencing ACS are also at higher risk of in-hospital and long-term mortality as compared to non-cancer patients. In this review, we will provide an overview on the available evidence of the relationship between ACS and cancer, in terms of clinical manifestations, possible underlying mechanisms, and therapeutic and prognostic implications.


2021 ◽  
Vol 28 (1) ◽  
pp. e100341
Author(s):  
Haiquan Li ◽  
Edwin Baldwin ◽  
Xiang Zhang ◽  
Colleen Kenost ◽  
Wenting Luo ◽  
...  

ObjectivesPrior research has reported an increased risk of fatality for patients with cancer, but most studies investigated the risk by comparing cancer to non-cancer patients among COVID-19 infections, where cancer might have contributed to the increased risk. This study is to understand COVID-19’s imposed HR of fatality while controlling for covariates, such as age, sex, metastasis status and cancer type.MethodsWe conducted survival analyses of 4606 cancer patients with COVID-19 test results from 16 March to 11 October 2020 in UK Biobank and estimated the overall HR of fatality with and without COVID-19 infection. We also examined the HRs of 13 specific cancer types with at least 100 patients using a stratified analysis.ResultsCOVID-19 resulted in an overall HR of 7.76 (95% CI 5.78 to 10.40, p<10−10) by following 4606 patients with cancer for 21 days after the tests. The HR varied among cancer type, with over a 10-fold increase in fatality rate (false discovery rate ≤0.02) for melanoma, haematological malignancies, uterine cancer and kidney cancer. Although COVID-19 imposed a higher risk for localised versus distant metastasis cancers, those of distant metastases yielded higher overall fatality rates due to their multiplicative effects.DiscussionThe results confirmed prior reports for the increased risk of fatality for patients with COVID-19 plus hematological malignancies and demonstrated similar findings of COVID-19 on melanoma, uterine, and kidney cancers.ConclusionThe results highlight the heightened risk that COVID-19 imposes on localised and haematological cancer patients and the necessity to vaccinate uninfected patients with cancer promptly, particularly for the cancer types most influenced by COVID-19. Results also suggest the importance of timely care for patients with localised cancer, whether they are infected by COVID-19 or not.


2019 ◽  
Vol 76 (9) ◽  
pp. 968-972
Author(s):  
Rade Milic ◽  
Sanja Sarac ◽  
Biljana Lazovic-Popovic ◽  
Miroslav Dinic

Introduction. Deep vein thrombosis and pulmonary embolism, known as venous thromboembolism, constitute a major global burden of disease. Both entities share the same risk factors. Psoriasis is a common, chronic skin disease. It also presents multisystemic inflammation, mainly affecting skin and joints, but it is also associated with the significant cardiovascular and metabolic states and comorbidities, on the so-called ?psoriatic march?. Case report. We presented a 78-year-old female patient, with psoriasis associated with pulmonary embolism which is accidentally discovered. We did not find any other predisposing factor of this disease (primary or secondary thrombophilia), except hyperhomocysteinemia. The patient was treated with low molecular weight heparin (enoxaparin), followed by the administration of an oral vitamin K antagonist (warfarin sodium) in the weight adjusted regimens. Additionally, we recommended vitamin B complex, including folate. Supposed link between hyperhomocysteinemia and psoriasis was the decreased serum folate level as the result of increased vitamin utilization in the skin because of increased DNA synthesis. Conclusion. The reported case reflects existing literary knowledge about the increased risk of VTE and arterial thromboembolic events in the psoriatic patients. The highest risk appears in the patients with a severe disease and may be a consequence of systemic inflammation and hyperhomocysteinemia.


2010 ◽  
Vol 103 (02) ◽  
pp. 338-343 ◽  
Author(s):  
Shankaranarayana Paneesha ◽  
Aidan McManus ◽  
Roopen Arya ◽  
Nicholas Scriven ◽  
Timothy Farren ◽  
...  

SummaryVenous thromboembolism (VTE) is a clinically important complication for both hospitalised and ambulatory cancer patients. In the current study, the frequency, demographics and risk (according to tumour site) of VTE were examined among patients seen at outpatient DVT (deep-vein thrombosis) clinics. Of 10,015 VTE cases, 1,361 were diagnosed with cancer, for an overall rate of cancer-associated VTE of 13.6% in this outpatient population. Patients with cancer-associated VTE were significantly older than cancer-free VTE cases (66.4 ± 12.7 vs. 58.8 ± 18.5 years; p<0.0001). The frequency of cancer-associated VTE peaked earlier among females than males, occurring in the sixth (137/639, 21.4% vs. 98/851, 11.3%; p<0.001) and seventh decades (213/980, 21.7% vs. 197/1096, 18%; p=0.036). VTE was described most frequently in common cancers – breast, prostate, colorectal and lung (56.1% of cases). The risk of VTE varied widely across 17 cancer types. Calculating odds ratios (OR) to assess the effect size of cancer type on VTE risk, the highest odds were observed for patients with pancreatic cancer (OR 9.65, 95% confidence interval [CI] (5.51–16.91). Tumours of the head and neck had higher odds than previously reported (OR 8.24, 95% CI 5.06–13.42). Reduced risk estimates were observed for skin cancers (melanoma and non-melanoma: OR 0.89, 95% CI 0.42–1.87; OR 0.74, 95% CI, 0.32–1.69, respectively). We conclude that outpatients have a similar rate of cancer-associated VTE as VTE patient populations previously reported, that cancer-associated VTE occurs in an older age group and earlier in females and that outpatients exhibit distinct tumour site-specific risk from that described among hospitalised cancer patients.


Hematology ◽  
2016 ◽  
Vol 2016 (1) ◽  
pp. 206-207 ◽  
Author(s):  
Lisa Baumann Kreuziger ◽  
Michael Streiff

Abstract A 68-year-old man developed a right femoral vein deep vein thrombosis and bilateral pulmonary embolism while receiving chemotherapy for stage IV prostate cancer. His creatinine at diagnosis is 1.4 mg/dL, with an estimated clearance of 63 mL/min. In patients with cancer, should low-molecular-weight heparin treatment be dosed according to weight, or adjusted using anti-Xa levels?


2021 ◽  
Vol 10 (Supplement_1) ◽  
Author(s):  
BV Silva ◽  
C Mendonca ◽  
N Cunha ◽  
P Silverio Antonio ◽  
T Rodrigues ◽  
...  

Abstract Funding Acknowledgements Type of funding sources: None. Background Pulmonary embolism (PE) is more prevalent in patients with cancer. D-dimers are a less useful test in such patients due to less specificity. Several algorithms have been developed as an alternative to the fixed d-dimer cutoff,  aiming to avoid the excessive use of computed tomography pulmonary angiography (CTPA), but it is not clear which is the most accurate algorithm in PE patients with cancer. Objective To compare the efficacy of 4 algorithms to rule out pulmonary embolism (fixed Ddimer cutoff, age-adjusted, YEARS and PEGed) in patients with active cancer. Methods Retrospective study of consecutive outpatients who presented to the emergency department and underwent CTPA for PE suspicion from April 2019 to February 2020. The clinical-decision algorithms were retrospectively applied. In fixed and age-adjusted cutoffs, high probability patients are directly selected for CTPA and the others perform CTPA if DDimer ≥500µg/L or age x10 µg/L within patients over 50 years, respectively. YEARS includes 3 items (signs of deep vein thrombosis, haemoptysis and whether PE is the most likely diagnosis): patients without any YEARS items and Ddimer ≥1000ng/mL or with ≥1 items and Ddimer 500ng/mL perform CTPA. In the PEGeD, patients with high clinical probability or with intermediate and Ddimer &gt;500µg/L or low probability and Ddimer &gt;1000 µg/L are selected for CTPA. Results Of 409 patients with suspected PE, 87 patients (21,3%) had cancer. The prevalence of PE was 38% in cancer patients and 35% in patients without cancer (p &gt; 0.05). Age-adjusted cut-off, compared to the conventional cutoff, had an AUC significantly higher (0.68 vs 0.61, p = 0.005). Despite both having 100% sensitivity, age-adjusted cutoff had a significant higher specificity compared to conventional cut-off (44% vs 35%, p &lt; 0.05). Both YEARS and PEGED algorithms had significantly lower sensitivity (p = 0.003 and p = 0.002, respectively) and higher specificity (p &lt; 0.001, for both) compared to conventional cutoff in patients with active cancer. The AUC of these two algorithms was not significantly different compared to conventional cutoff (p = 0.08 and p = 0.78, respectively). Conclusion Considering our results, age-adjusted cut-off seems to be the most accurate algorithm to rule out pulmonary embolism in active cancer patients. Sen(%)Spec(%)Conventional10022Age-adjusted10035YEARS9144PEGED9130Abstract Figure. AUC of four algorithms


2013 ◽  
Vol 31 (15_suppl) ◽  
pp. 5576-5576
Author(s):  
Hedy S Rennert ◽  
Gad Rennert ◽  
Ofer Lavie ◽  
Shlomi Sagi ◽  
Michele Leviov ◽  
...  

5576 Background: Deep vein thrombosis and pulmonary embolism - venous thromboembolic events (VTEs) - are associated with significant morbidity and increased risk of mortality in cancer patients. Ovarian cancer patients are at a particularly increased risk for VTEs. Statins and aspirin have been shown to reduce the risk of VTEs in the general population in randomized trials. However, the effect of these medications on the incidence of VTEs in ovarian cancer patients has not been studied. Methods: Patients diagnosed with ovarian cancer between years 2000 and 2011 were identified through the Israeli Cancer Registry (ICR). Patients insured by Clalit Health Services, the largest HMO in Israel, were included. Data regarding medication use, chronic diseases and VTE diagnosis were extracted from the computerized database. Patients taking Warfarin or Low Molecular Weight Heparin for 3 months or longer were excluded. Statistical analysis was performed using SPSS (v 18). Use of medications was analyzed as a time dependent covariate in a Cox regression model. Results: Of 1,886 patients 179 (9.5%) had a VTE during a median follow up of 3.13 years. 95 patients (5%) had a VTE 2 years after diagnosis of ovarian cancer. In a multivariate analysis use of chemotherapy and stage 3 or 4 at presentation were associated with an increased risk for VTE's 2 years after diagnosis. Age was associated with a trend for increased risk. Statins were used by 43.2% of the patients, and 31.9% used aspirin. Aspirin use was associated with a reduced incidence of a VTE, which was borderline statistically significant (p=0.054). Statin use did not affect the incidence of VTE's in the group of ovarian carcinoma patients. Conclusions: Our results suggest that in patients with ovarian cancer aspirin use is a possible protector from deep vein thrombosis and pulmonary embolism. Prospective trials are warranted to assess the benefit of aspirin and statins for prevention of VTE's in the high risk population of ovarian cancer patients. [Table: see text]


Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 3655-3655
Author(s):  
Mina Gendy ◽  
Marie Anne Christine Buteau ◽  
Marc Braunstein

Background: Superficial vein thrombosis (SVT) has been historically considered to have a low risk of distal embolization and mortality, typically not warranting anticoagulation in the absence of underlying risk factors for thrombosis. However, recent studies of outcomes of SVT in patients without malignancy revealed significantly increased incidence of deep venous involvement at the time of presentation, as well as higher than expected rates of complications, reported in up to 10% of patients (Decousus et al. Ann Int Med(152)2010:218-224). However, outcomes of SVT in patients with cancer have not been well studied, despite the known increased risk of malignancy-associated thrombosis. In this study, we examined the rate of complications in patients who developed SVT in the setting of active malignancy. Methods: A retrospective single-center chart review of electronic medical records along with a corresponding database of radiology reports from NYU Winthrop Hospital from 2013 to 2019 was performed to identify patients with cancer who also had image-confirmed SVT. Patients were included if they had a synchronous or subsequent deep vein thrombosis (DVT) or pulmonary embolism (PE) during treatment, but excluded if they had a history of thrombosis prior to their cancer diagnosis, primary hypercoagulable disorder, or on therapeutic anticoagulation at the time of SVT diagnosis. Descriptive statistics for the overall sample, as well as a subgroup of subjects who were not treated at SVT diagnosis, were performed using SAS version 9.4 (SAS Institute Inc., Cary, NC). Results: 490 patients were noted to have a diagnosis of SVT and cancer, and of these, 40 met the enrollment criteria. Demographic data are shown in the table below. Among the 40, 21 patients had upper extremity, and 19 had lower extremity SVT. As shown in the table, 15 patients (37.5%) had a concurrent thromboembolism at the time of SVT diagnosis. An intervention was provided in 26 (69% full dose and 11% prophylactic dose anticoagulation, 15.3% antiplatelet therapy, and 3.8% vena cava filter placement). Of these 26 patients, one who received prophylactic anticoagulation developed a subsequent DVT. This patient had stage IV colon cancer and recent surgical resection, and developed SVT associated with intravenous access. Among the 14 patients with SVT who were not treated, 6 (43%) developed subsequent complications including one with DVT at the same extremity, 2 with DVT at a different location, and 3 with recurrence of the underlying SVT. Five of these were stage IV gastrointestinal cancers (including 3 patients with pancreatic cancer, 1 with gastric, and 1 with cholangiocarcinoma), and one had stage IV ovarian cancer. Considering the 8 patients who were not treated and did not develop complications, there was no dominant cancer type (3 were stage IV breast cancer, 1 had stage I pancreatic cancer, 1 had stage III hepatocellular carcinoma, and one had chronic lymphocytic leukemia). Conclusions: This study reveals a greater degree of concurrent SVT complications in the setting of malignancy compared to prior reports in patients without cancer. The rate of complications were higher in those patients who did not receive treatment (either prophylactic or therapeutic) for their SVT or who had metastatic disease. Although the overall incidence of SVT in cancer patients is low, data presented here suggest a higher than expected rate of complications within a 3 month span following SVT diagnosis in the setting of malignancy compared to prior reports of patients without malignancy. Prospective studies are needed to assess the benefit of anticoagulation in decreasing the risk for SVT complications in patient with active cancer. Table Disclosures Braunstein: Celgene: Consultancy, Other: Advisory boards; Takeda: Consultancy, Other: Advisory Board; Amgen: Consultancy, Other: Advisory Board; AstraZeneca: Consultancy, Other: Advisory Board; Janssen: Consultancy, Other: Advisory Board, Research Funding; Verastem: Consultancy, Other: Advisory Board.


Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 4005-4005
Author(s):  
Donald Doll

Abstract 4005 Poster Board III-941 Background There is an increased risk of thrombo-embolism in patients receiving erythropoeitic stimulating agents (ESAs) in the treatment of anemia due to cancer and chemotherapy as well as in patients with chronic renal failure. This fact coupled with evidence of the negative impact on survival in some patients with cancer has prompted a change in the FDA label and restricted the use of ESAs. The exact incidence of thrombo-embolism etiologically related to ESAs in community cancer practices is not known. In this retrospective study we examined the relationship between the administration of ESAs and thrombo-embolism in patients treated after initiating the more conservative use of such agents based on label change. Methods One-hundred fifty-eight cases of thrombo-embolism and central catheter occlusion observed between August 2007 and May 2009 were identified through the electronic medical records (EMR) database at Gabrail Cancer Center. Likewise, all patients who received ESAs during the same time period were identified through the EMR. Records of all patients were examined to verify diagnosis, confirm data, and validate timing of administration of the ESAs. Results A total of 496 patients received ESAs during the study period. Of these patients, 158 developed thrombo-embolism or central catheter occlusion. There were 128 patients with cancer and 34 had non-cancerous diagnoses with mean age of 62 and M:F of 4:1. Of the 128 patients with cancer 99 patients developed uncomplicated catheter occlusion and 39 developed DVT and/or pulmonary embolism. Seventy-four of the 99 patients who had catheter occlusion had received ESAs (74%). Of the 39 patients who developed DVT and pulmonary embolism 26 were treated with ESAs (67%). Of the 99 patients who developed catheter occlusion 51 (51%) received ESAs prior to catheter occlusion of the 39 patients who had DVT and PE 19 (48%) of the events happened after ESAs were initiated. The total number of patients who received ESAs during the same time period was 496. Only 32% of these patients developed thrombo-embolism and catheter occlusion. However, only 114 patients (23%) experienced a thrombotic episode after ESAs were initiated. This did not differ significantly from the incidence of thrombosis either in the form of catheter occlusion, deep vein thrombosis, or pulmonary embolism in this patient population. Conclusion Although some studies have shown an increased incidence of thromboembolism in cancer patients receiving ESAs, such studies were performed at a time when the use of these agents was more liberal in order to increase the Hb to normal or above normal levels. In this community-based practice study that included patients treated after the label change, the incidence was not greater than that seen in cancer patients not receiving ESAs. However, a prospective clinical trial is needed to confirm these findings especially after the label change that has restricted the use of ESAs. 3(Transmittal 80, Pub 100-03 Medicare National Coverage Decision, eff. 7/30/2007) Disclosures: No relevant conflicts of interest to declare.


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