Prevalence of neoplasms in 415 patients with deep venous thrombosis
(Portuguese PDF version)

Miriam Aparecida Linares,1 Tais Elisabete Rodrigues,1 Karen Kazue Hirato,1 Juliana D. de Oliveira,2 Selma Regina Oliveira Raimundo,3 José Maria Pereira de Godoy4

1. Resident physician, Angiology and Cardiovascular Surgery Service, Faculdade de Medicina Estadual de São José do Rio Preto (FAMERP), São José do Rio Preto, SP, Brazil.

2. Undergraduate student, FAMERP, São José do Rio Preto, SP, Brazil.

3. Assistant Professor, Angiology and Cardiovascular Surgery Service, FAMERP, São José do Rio Preto, SP, Brazil.

4. Physician. Associate professor, Angiology and Cardiovascular Surgery Service, FAMERP, São José do Rio Preto, SP, Brazil.


Correspondence:
José Maria Pereira de Godoy
Rua Floriano Peixoto, 2950
CEP 15020-010 - São José do Rio Preto, SP, Brazil
E-mail: godoyjmpiopreto.com.br


ABSTRACT

Objective: The purposes of this study were to assess the prevalence of neoplasms in 415 patients with deep venous thrombosis and to identify its different types.

Method: The presence of neoplasms in 415 patients with deep venous thrombosis of the lower limbs was evaluated in a prospective study. The age of patients treated in the vascular surgery department varied from 11 to 92 years with mean age of 55.2 years. Diagnosis of thrombosis was performed using a duplex scan and, in case of doubt, the results were confirmed by phlebology. Clinical history and physical examination were performed for all patients. Biochemical, imaging and surgical examinations, as well as biopsies, were performed when required. Among the main laboratorial tests, in cases of clinical suspicion, there were thoracic x-ray, endoscopy, abdominal ultrasound, computerized tomography and magnetic resonance. Specific clinical evaluations were requested for urological and gynecological complaints. All patients with previous histories of neoplasms were excluded from the investigation.

Results: A total of 58 (13.9%) neoplasms were detected in 415 patients suffering from deep venous thrombosis, 27.5% of which developed in the gastrointestinal tract, 15.5% in the gynecological system, 8.6% in the respiratory system, 6.8% in the tegumental system, 3.4% in the skeletal system, 1.7% retroperitoneal and 1.7% in the reticuloendothelial system.

Conclusion: As a conclusion, we may say that patients suffering from deep venous thrombosis present with a high incidence of neoplasms, suggesting that screening is a procedure of great importance.

Key words: prevalence, neoplasms, thrombosis.

J Vasc Br 2004;3(4):347-50


Neoplasms are known as independent risk factors for deep venous thrombosis (DVT).1,2 Among mechanisms that trigger them off are the synthesis of procoagulant factors produced by tumoral cells, monocytes or macrophages; platelet aggregation abnormalities; antineoplastic therapy, and comorbities such as venous stasis.3-5 Venous stasis can be a consequence of complications that limit patients to their beds and thus reduce their mobility. Coagulation activation is found in around 90% of patients with neoplasms. However, mechanisms of hypercoagulability are less clear.6,7 Around 10 to 15% of patients with cancer present venous thromboembolism.8,9 DVT has been reported as the first clinical manifestation of a neoplasm. Therefore, it constitutes a paraneoplastic syndrome.5,9,10 Lung, pancreatic, stomach, intestinal, ovarian, and prostatic neoplasms are most commonly associated with thromboembolism.11,12

The purposes of this study were to assess the prevalence of neoplasms in 415 patients with DVT and to identify its different types.

MATERIALS AND METHODS

The presence of neoplasms in 415 consecutive patients who had DVT of lower limbs was evaluated in a prospective study performed in a vascular surgery service. Two hundred and twenty-one patients were female, and 194 were male. Ages ranged from 11 to 92 years, and mean age was 55.2 years. All patients underwent a duplex scan and, in case of doubt concerning diagnosis, phlebography was performed as well.13 Criteria considered to show the presence of DVT by duplex scan included: presence of spontaneous flow, absence of phasicity of flow, and flow velocity. Clinical history, physical and biochemical examinations, imaging, biopsies, and surgeries were performed when indicated. All diagnoses of neoplasms were confirmed by histology. Thoracic radiography, endoscopy, abdomen ultrasound, computerized tomography, and magnetic resonance were required in cases of clinical suspicion, as well as urological evaluation for men and gynecological evaluation for women. All patients who presented DVT were included in the study. Patients with previous diagnosis of neoplasm were excluded. For statistical evaluation we calculated percentages and mean values.

RESULT

Fifty-eight neoplasms were detected in 415 patients, indicating a prevalence of 13.9%, 27.5% of which developed in the gastrointestinal tract, 17.2% in the gynecological system, 17.2% in the central nervous system, 15.5% in the urological system, 8.6% in the respiratory system, 6.8% in the tegumental system, 3.4% in the skeletal system, 1.7% in the retroperitoneal system, and 1.7% in the reticuloendothelial system.

DISCUSSION

This study detected a high prevalence of neoplasms in patients with DVT (13.9%), when the prevalence of congenital thrombophilia, such as the deficiency of antithrombin III, protein C, and protein S, was evaluated at the vascular surgery service of our hospital.13-15 The result of this study emphasizes that thrombotic events are significant paraneoplastic manifestations. On the other hand, more intense prophylaxis should be considered in cases of patients with neoplasms and exposed to risk factors, such as surgery, immobilization in bed, chemotherapy, catheter implantation, and others. The literature associates idiopathic thromboembolism with neoplasms in 7 to 8% of the cases. It can increase to 17% in cases of rethrombosis.16

When screening for cancer in venous thrombosis patients, an attentive clinical evaluation should be considered, as neoplasms may not be manifested yet. The examination may include digital rectal examination, fecal occult blood test, urine tests, blood cell count, renal function test, carcinoembryonic antigen test, thoracic radiography, and gynecological and urological evaluation. Invasive and costly examinations, like abdomen ultrasound, computerized tomography, magnetic resonance, and endoscopy should be considered in each case, depending on the clinical suspicion.

Another factor to be considered is that an association of venous thromboembolism with neoplasms presents a worse prognosis, and it is already proved that an early diagnosis does not increase life expectancy. Besides, we should consider the psychological aspects of a routine invasive investigation.3,17,18

In the present study, the gastrointestinal tract, and the gynecological and urological systems were most affected. The central nervous system also had a high rate of occurrences, which can be interpreted as an alert for this kind of occurrence. Lungs, as isolated organs, were of great importance. With respect to isolated organs, the lungs were importantly affetcted, justifying the need for careful screening.

Initial treatment of DVT in patients with cancer does not differ from the treatment given to other patients.19 It should continue for 6 months after the first episode of DVT is reported, but in cases of thromboembolic recurrence, anticoagulation should be extended.20 In some types of cancer, anticoagulation is recommended for an indefinite time. However, there is no consensus about that and, therefore, an individualized evaluation of each case is the best indication. Patients with cancer have a higher risk of rethrombosis and bleeding. Thus, a trade-off must be considered between risks and anticoagulation therapy.

The Fundamental Research in Oncology and Thrombosis (FRONTLINE) made the first global survey of thrombosis and cancer. The study analyzed items such as the anticoagulation therapy after an episode of pulmonary thromboembolism (PTE) in surgical or clinical patients. The duration of anticoagulation ranged from 3 to 6 months (63% for PTE in surgical patients, 72% for DVT in clinical patients, and 58% for PTE in clinical patients). In 19% of the patients anticoagulation was present for 7 to 12 months, and in 18% for an indefinite time.21,22

CONCLUSION

As a conclusion, we may say that patients suffering from DVT present a high prevalence of neoplasms, suggesting individualized screening.

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