Abstract
Objectives
Gonadal vein thrombosis is an uncommon but serious condition that can be fatal if it goes unnoticed. Up to 80% of cases occur in patients after delivery, hysterectomy, or lymphadenectomy for gynecological neoplasms. The objective of this study was to determine the incidence of gonadal vein thrombosis using computed tomography (CT) imaging at our center and to describe associated risk factors.
Methods
A retrospective, single-center, observational study was conducted at King Abdulaziz Medical City in Jeddah, Saudi Arabia. Data were collected for all patients diagnosed with incidental gonadal-vein-thrombosis using contrast-enhanced computed tomography imaging of the abdomen and pelvis between January 2005 and December 2017. We included all patients with incidental findings of gonadal vein thrombosis and excluded those with incomplete data.
Results
In total, 58/68,268 (0.08%) patients were included. Fifty-seven patients were females, and only one was male. The mean age (years) of the patients was 50.0±15.0 (range 4-87). Thirty-four patients (59%) had right gonadal vein thrombosis, 20 (34%) had thrombosis on the left side, and four (7%) had bilateral thrombosis. Nineteen patients (33%) had undergone pelvic surgery previously. Forty-four patients (76%) had a malignancy at the time of diagnosis. Forty-two patients (72%) were treated with anticoagulants after the diagnosis.
Conclusion
Gonadal vein thrombosis is a rare clinical entity with vague clinical presentation. The incidence in the oncology population is similar to the reported incidence in the obstetric population. Initiation of anticoagulation therapy is important to treat this condition and limit complications.
Keywords: ovarian vein, gonadal vein, thrombosis, computed tomography, imaging
Introduction
Gonadal vein thrombosis (GVT) is an exceedingly uncommon but serious condition that can be fatal if it goes unnoticed, and it is often accompanied by complications such as thrombophlebitis and sepsis [1-3]. The nature of GVT and its distinct characteristics were identified initially in a case report published in 1956 by Austin [4].
Almost 80% of GVT cases in the literature were reported for patients after delivery, hysterectomy, and lymphadenectomy for gynecological neoplasms [1,5-6]. GVT occurs most commonly (80%-90%) on the right [1-2,7]. In one study, the incidence of GVT was around 0.02% for vaginal deliveries and 0.1% for cesarean deliveries [8]. In the same study, 0.7% of twin deliveries via cesarean section were complicated by GVT, whereas no cases of GVT were observed for twin deliveries via the vaginal route.
The development of idiopathic GVT is even rarer, and we are not aware of its incidence being reported in the literature; it is mainly described in relation to pregnancy [6,8]. Pregnancy, pelvic inflammatory disease, pelvic surgery, and malignancy have been reported in association with the development of GVT [8-9]. The usual clinical presentation of GVT varies from asymptomatic to non-specific abdominal pain. Patients rarely present with acute abdominal pain [10].
Ultrasound, computed tomography (CT) imaging, and magnetic resonance imaging (MRI) can be used for the diagnosis of GVT. However, contrast-enhanced CT imaging of the abdomen and pelvis is the most reliable of these, with 100% sensitivity and 99% specificity [6]. The classical imaging findings are filling defects and enlargement of the gonadal vein [11]. Gonadal veins have extensive communication with the gonads and perineum, and this can facilitate the entry of infections [1].
In this study, we aimed to determine the 13-year incidence of GVT at a single tertiary hospital using CT imaging. We further describe GVT-associated risk factors.
Materials and methods
A retrospective, single-center, observational study was conducted at King Abdulaziz Medical City in Jeddah, Saudi Arabia. The study was approved by the Institutional Review Board of King Abdullah International Medical Research Center. Data collection was performed by searching the center’s Radiology Information System for all patients diagnosed with incidental GVT using contrast-enhanced CT imaging of the abdomen and pelvis between January 2005 and December 2017. The search terms were “gonadal vein thrombosis” and “ovarian vein thrombosis.” The Hospital Information System and the Picture Archiving and Communication System were used to collect patient demographic profiles (namely, age and gender), clinical characteristics (namely, diagnosed diseases, comorbidities, previous surgeries, and malignancies), radiological features (namely, radiological modality, vein size, and thrombus size), and treatment parameters (namely, type of treatment, length of treatment, and outcome). All patients with an incidental finding of GVT were included, and those with incomplete data were excluded. Data were recorded in an encrypted Microsoft Excel (Microsoft Corporation, Redmond, WA) file for analysis.
All numerical values obtained were presented using simple descriptive statistics: means and standard deviations for continuous data, frequencies and percentages for categorical data. IBM SPSS Statistics for Windows version 21.0 (IBM Corp., Armonk, NY) was used for data analysis. All data collection sheets were anonymous, with no identifiers used. Privacy and confidentiality of information were completely maintained.
Results
In total, 58 patients were diagnosed with incidental GVT using contrast-enhanced CT imaging during the study period, an overall incidence of 0.08%. Demographics, subject, and GVT characteristics are shown in Table 1. Fifty-seven patients (98%) were females and only one (2%) was male. The mean age (years) of the patients was 50.0±15.0 (range 4-87). Thirty-four patients (59%) had right GVT while 20 (34%) had left GVT. Only four patients (7%) had bilateral GVT. The mean diameter of the thrombosed vein was 10.09±3.56 mm (range 4.05-21.49 mm). Twenty-nine patients (50%) had acute thrombi at the time of imaging while the other 50% had chronic thrombi (i.e., acute thrombosis is considered whenever there is a central thrombus distending the lumen with surrounding contrast media; otherwise, chronic thrombosis is considered). All patients with bilateral GVT had chronic thrombi. Nineteen patients (33%) had concurrent thrombosis of another vein, most commonly the renal vein or the inferior vena cava. Seven patients (12%) had evidence of pulmonary embolism. Nineteen patients (33%) had undergone pelvic surgery previously. Forty-four patients (76%) had a malignancy at the time of diagnosis; of these, the most common sites affected were the breast (9 patients “20.5%”) and the colon (8 patients “18.2%”). Other sites included the uterus (4 patients “9.1%”), brain (3 patients “6.8%”), urinary bladder (3 patients “6.8%”), kidney (2 patients “4.5%”), lung (2 patients “4.5%”), small bowel (2 patients “4.5%”), shoulder (2 patients “4.5%”), ovaries (1 patient “2.3%”), stomach (1 patient “2.3%”), pancreas (1 patient “2.3%”), and gallbladder (1 patient “2.3%”), whereas other malignancies included lymphoma (2 patients “4.5%”), cholangiocarcinoma (1 patient “2.3%”), leukemia (1 patient “2.3%”), and Wilms (1 patient “2.3%”). Forty-two patients (72%) were treated with anticoagulants after the diagnosis of GVT while 16 (28%) were not treated at our center due to death prior to initiation of treatment, refusal to be treated, or preference to be treated at another hospital.
Table 1. Demographics, subject, and gonadal vein thrombosis (GVT) characteristics.
Variable | Total Subject (n = 58) | |
Age in years “Mean (Standard deviation)” | 50.0 (15.0) | |
Gender “n (%)” | Male | 1 (2%) |
Female | 57 (98%) | |
GVT side “n (%)” | Right | 34 (59%) |
Left | 20 (34%) | |
Bilateral | 4 (7%) | |
Thrombosed vein diameter in millimeter “Mean (Standard deviation)” | 10.09 (3.56) | |
GVT acuity at the time of imaging “n (%)” | Acute | 29 (50%) |
Chronic | 29 (50%) | |
Concurrent thrombosis of another vein “n (%)” | 19 (33%) | |
Evidence of pulmonary embolism “n (%)” | 7 (12%) | |
Previous pelvic surgery “n (%)” | 19 (33%) | |
Malignancy at the time of diagnosis “n (%)” | 44 (76%) | |
Anticoagulants treatment “n (%)” | Yes | 42 (72%) |
No | 16 (28%) |
Discussion
The incidence of GVT from CT images in our study was 0.08%, with the right gonadal vein being involved in 59% of the patients diagnosed as such. The most common risk factor among the patients in our series was malignancy. The prevalence of malignancies among the patients is probably because ours is an oncology center. The increased susceptibility of the right side may be attributed to the longer length of the right gonadal vein than that of the left, and an increased absence of competent valves in the right compared to that in the left gonadal vein [5,12]. In addition, the antegrade blood flow in the right gonadal vein favors bacterial infection unlike the retrograde blood flow in the left gonadal vein [13]. Nevertheless, a higher incidence of thrombosis in the left than in the right ovarian vein was reported in one study [14]. Bilateral thrombi are observed in 11%-14% of cases [12-13]. In our study, the right gonadal vein was involved in 59% of patients, which is lower than the reported rate in the literature (i.e., 70%-90%), whereas the left gonadal vein was involved in more than 30% of patients, which is higher than the reported rate in the literature (i.e., 24%) [2,15]. Bilateral involvement was observed in 7% of patients, which is lower than the reported rate in the literature (i.e., 14%) [12-13,15].
Several dangerous complications may occur with GVT, including pulmonary embolism, sepsis with multiorgan failure, an extension of the thrombus into the inferior vena cava, iliac vein, or renal vein, and an increased risk of ovarian infarction [8-9]. Pulmonary embolism is an infrequent complication reported in the range of 13%-33% [8]. In our study, 33% of patients exhibited concurrent thrombosis of other veins at the time of diagnosis. In addition, 12% developed pulmonary embolism, which is in agreement with the reported rate in other studies [2,16].
Malignancy is a recognized prothrombotic condition with an incidence rate of as high as 20% in cases of venous thromboembolism [17]. Cancer is associated with changes in blood flow, damage to vascular endothelium, and changes in clotting factors [18]. Venous thromboembolism is associated with increased morbidity and considered a common cause of death in cancer patients [19]. Our results indicated that 76% of patients had a malignancy.
The management of GVT is mainly performed using anticoagulation therapy for three to six months. Extension of the thrombus to the renal vein and/or inferior vena cava is treated similar to pulmonary embolism [20]. Surgical management is reserved for patients with contraindications to anticoagulants and for those who develop pulmonary emboli despite conservative therapeutic management [21-22]. In our study, 72% of patients were successfully treated with anticoagulants. The remaining patients were not treated at our center due to death prior to the initiation of treatment, refusal to be treated, or preference to be treated at another hospital.
The study is limited due to its small sample size, retrospective nature, and all cases included were oncology cases from an oncology center. Yet, it showed that the incidence of GVT in oncology patients is similar to the overall population. Multicenter studies with a larger, more variable sample can be further assessed.
Conclusions
This study revealed the incidence of GVT using CT scans and described its associated risk factors. GVT is a rare clinical entity with vague clinical presentation. Initiation of anticoagulation therapy is important to treat this condition and limit complications.
The content published in Cureus is the result of clinical experience and/or research by independent individuals or organizations. Cureus is not responsible for the scientific accuracy or reliability of data or conclusions published herein. All content published within Cureus is intended only for educational, research and reference purposes. Additionally, articles published within Cureus should not be deemed a suitable substitute for the advice of a qualified health care professional. Do not disregard or avoid professional medical advice due to content published within Cureus.
The authors have declared that no competing interests exist.
Human Ethics
Consent was obtained or waived by all participants in this study. King Abdullah International Medical Research Center issued approval IRBC/1253/16
Animal Ethics
Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.
References
- 1.Abdominal thromboses of splanchnic, renal and ovarian veins. De Stefano V, Martinelli I. https://doi.org/10.1016/j.beha.2012.07.002. Best Pract Res Clin Haematol. 2012;25:253–264. doi: 10.1016/j.beha.2012.07.002. [DOI] [PubMed] [Google Scholar]
- 2.Postpartum ovarian vein thrombophlebitis. A review. Dunnihoo DR, Gallaspy JW, Wise RB, Otterson WN. Obstet Gynecol Surv. 1991;46:415–427. doi: 10.1097/00006254-199107000-00002. [DOI] [PubMed] [Google Scholar]
- 3.Postpartum ovarian vein thrombosis and venous anatomical variation. Abrantes J, Teixeira E, Gomes F, Fernandes C. BMJ Case Rep. 2019;12:0. doi: 10.1136/bcr-2018-228399. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Massive thrombophlebitis of the ovarian veins. A case report. Austin OG. Am J Obstet Gynecol. 1956;72:428–429. doi: 10.1016/0002-9378(56)90130-2. [DOI] [PubMed] [Google Scholar]
- 5.Ovarian vein thrombosis in the nonpregnant woman: an overlooked diagnosis. Harris K, Mehta S, Iskhakov E, Chalhoub M, Maniatis T, Forte F, Alkaied H. https://doi.org/10.1177/2040620712450887. Ther Adv Hematol. 2012;3:325–328. doi: 10.1177/2040620712450887. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Diagnosis and management of ovarian vein thrombosis in a healthy individual: a case report and a literature review. Kodali N, Veytsman I, Martyr S, Lu K. https://doi.org/10.1111/jth.13584. J Thromb Haemost. 2017;15:242–245. doi: 10.1111/jth.13584. [DOI] [PubMed] [Google Scholar]
- 7.Postpartum ovarian vein thrombosis: clinical case. Ribeiro A, Brás R, Moleiro ML, Braga A, Braga J. https://doi.org/10.15761/OGR.1000136 J Clin Obstet, Gynecol Infertil. 2019;3:1044. [Google Scholar]
- 8.Pregnancy and non-pregnancy related ovarian vein thrombosis: clinical course and outcome. Rottenstreich A, Da'as N, Kleinstern G, Spectre G, Amsalem H, Kalish Y. https://doi.org/10.1016/j.thromres.2016.09.001. Thromb Res. 2016;146:84–88. doi: 10.1016/j.thromres.2016.09.001. [DOI] [PubMed] [Google Scholar]
- 9.Ovarian vein thrombosis in pregnancy and the puerperium - a case series. Mone F, McKeown G, Adams B. https://doi.org/10.3109/01443615.2015.1009420. J Obstet Gynaecol. 2015;35:853–854. doi: 10.3109/01443615.2015.1009420. [DOI] [PubMed] [Google Scholar]
- 10.The natural history and treatment outcomes of symptomatic ovarian vein thrombosis. Labropoulos N, Malgor RD, Comito M, Gasparis AP, Pappas PJ, Tassiopoulos AK. https://doi.org/10.1016/j.jvsv.2014.07.008. J Vasc Surg Venous Lymphat Disord. 2015;3:42–47. doi: 10.1016/j.jvsv.2013.10.018. [DOI] [PubMed] [Google Scholar]
- 11.Ultrasound, computed tomography, and magnetic resonance imaging of ovarian vein thrombosis in obstetrical and nonobstetrical patients. Virmani V, Kaza R, Sadaf A, Fasih N, Fraser-Hill M. https://doi.org/10.1016/j.carj.2010.08.002. Can Assoc Radiol J. 2012;63:109–108. doi: 10.1016/j.carj.2010.08.002. [DOI] [PubMed] [Google Scholar]
- 12.Ovarian vein thrombosis as a complication of laparoscopic surgery. Gupta A, Gupta N, Blankstein J, Trester R. https://doi.org/10.1155/2015/682941. Case Rep Obstet Gynecol. 2015;2015:682941. doi: 10.1155/2015/682941. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Ovarian vein thrombosis. Jenayah AA, Saoudi S, Boudaya F, Bouriel I, Sfar E, Chelli D. https://doi.org/10.11604/pamj.2015.21.251.6908. Pan Afr Med J. 2015;21:251. doi: 10.11604/pamj.2015.21.251.6908. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Ovarian vein thrombosis: analysis of patient age, etiology, and side of involvement. Gakhal MS, Levy HM, Spina M, Wrigley C. https://pubmed.ncbi.nlm.nih.gov/23550381/ Del Med J. 2013;85:45–50. [PubMed] [Google Scholar]
- 15.Ovarian vein thrombus: to treat or not to treat? Plastini T, Henry D, Dunleavy K. https://doi.org/10.1182/bloodadvances.2017006577. Blood Adv. 2017;1:1120–1123. doi: 10.1182/bloodadvances.2017006577. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Postpartum ovarian vein thrombosis. Dougan C, Phillips R, Harley I, Benson G, Anbazhagan A. https://doi.org/10.1111/tog.12295 Obstet Gynaecol. 2016;18:291–299. [Google Scholar]
- 17.Cancer-associated thrombosis: the when, how and why. Fernandes CJ, Morinaga LTK, Alves JL Jr, Castro MA, Calderaro D, Jardim CVP, Souza R. https://doi.org/10.1183/16000617.0119-2018. Eur Respir Rev. 2019;28:180119. doi: 10.1183/16000617.0119-2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Cancer-associated thrombosis: an overview of mechanisms, risk factors, and treatment. Abdol Razak NB, Jones G, Bhandari M, Berndt MC, Metharom P. https://doi.org/10.3390/cancers10100380. Cancers (Basel) 2018;10:380. doi: 10.3390/cancers10100380. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.High prevalence of recurrent thrombosis in subsets of cancer patients with isolated gonadal vein thrombosis: a single center retrospective study. Tanasanvimon S, Garg N, Viswanathan C, et al. https://doi.org/10.1016/j.thromres.2013.10.027. Thromb Res. 2014;133:154–157. doi: 10.1016/j.thromres.2013.10.027. [DOI] [PubMed] [Google Scholar]
- 20.Diagnosis and management of postpartum ovarian vein thrombosis. Bannow BTS, Skeith L. https://doi.org/10.1182/asheducation-2017.1.168. Hematology Am Soc Hematol Educ Program. 2017;2017:168–171. doi: 10.1182/asheducation-2017.1.168. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Surgical treatment of ovarian vein thrombosis. Carr S, Tefera G. https://doi.org/10.1177/1538574406291332. Vasc Endovascular Surg. 2007;40:505–508. doi: 10.1177/1538574406291332. [DOI] [PubMed] [Google Scholar]
- 22.A modern radiologic treatment for pelvic congestion syndrome associated with chronic pelvic pain and menstrual abnormalities. Kanter JR, Looney CB, Lue J, Gavrilova-Jordan LP. J Endometr Pelvic Pain Disord. 2017;9:297–300. [Google Scholar]