Received date: March 16, 2018; Accepted date: May 14, 2018 Published date: May 18, 2018
Citation: Yang M, Yang L, Wang F, Shi X, Wang H, et al. (2018) Case Report of Cardiac Metastasis from Cervical Squamous Carcinoma and its Literature Review. Gynecol Obstet Case Rep Vol.4: No.2:65. doi:10.21767/2471-8165.1000065
We reported a case of a symptomatic metastasis of squamous cell carcinoma of the uterine cervix (SCCUC) to the right ventricle, then to the right atrium and superior vena cava five years later than the first SCCUC diagnosis. Because of the persistent thrombocytopenia, the treatment was discontinued after only one cycle of reduced paclitaxel liposome five years ago. The patient died six weeks after the diagnosis of cardiac metastasis. We reviewed the literatures in last two decades for the epidemiology, clinical presentaion, diagnosis, treatment and prognosis of SCCUC with cardiac metastasis (SCCUCCM). Dyspnea and chest pain are the common clinical presentations. Echocardiography, cardiac computed tomography (CT) and cardiac magnetic resonance imaging (CMR) are recommended in diagnosis. The prognosis for cardiac metastasis is extremely poor, with a median survival time of 5 months. Thrombocytopenia is a negative factor in the survival time of SCCUC-CM. Aggressive therapy including surgical intervention, chemotherapy, and whole heart radiation therapy may prolong survival time.
Squamous cell carcinoma; Uterine cervix; Cardiac metastasis
It is common to find metastasis of squamous cell carcinoma of the uterine cervix (SCCUC) in lungs, liver, bones and supraclavicular lymph nodes. But intracavitary cardiac metastasis (CM) is rarely reported. In this study, a case of antemortem SCCUC with cardiac metastasis (SCCUC-CM) was reported, and the corresponding literatures were reviewed. In this study, we found that an early diagnosis of CM and aggressive treatment may prolong the survival time, especially for those with solitary metastasis and in good general conditions.
mass was 2.2 × 2 cm, squamous cell carcinoma, moderate differentiation with more than 1/2 myometrial invasion and vascular invasion. Follow-up examinations after the treatment included laboratory tests, gynecologic examinations and imaging tests (pelvic MRI, chest computed tomography [CT] and abdominal ultrasound). The results indicated no recurrence or metastasis. However, swellings in bilateral supraclavicular and mediastinal lymph nodes were identified in a follow-up CT 9 months later. The area of lymphatic metastasis was treated with radiation concurrent with four cycles of paclitaxel and cisplatin. After the treatment, swollen lymph nodes disappeared. In November 2017, the patient was admitted with a complaint of cough, chest pain and dyspnea. Electrocardiogram (ECG) displayed a flattened T-wave in leads III, aVL, aVF, V4-V6. The patient denied any history of cardiovascular disease. Further examinations were taken. The chest CT revealed the enlargement in the left axillary lymph nodes, bilateral hilar lymph nodes and multiple mediastinal lymph nodes, and the emboli in the right pulmonary artery (Figure 1). The transthoracic echocardiography revealed the presence of a mass occupying the right ventricle (Figure 2). The whole-body positron-emitting tomography computed tomography (PET-CT) showed the fluorodeoxyglucose (FDG) accumulation in the right ventricle, bilateral supraclavicular lymph nodes, left axillary lymph nodes, bilateral hilar lymph nodes and multiple mediastinal lymph nodes (Figure 3). Considering the medical history, the patient was suspected with cardiac and multiple lymph nodes metastasis of SCCUC. Biochemical tests revealed elevated fibrin degradation products (17.11 μg/ml; normal range, 0-5.00 μg/ml) and D-dimers (5.99 μg/ml; normal range, 0-0.55 μg/ml), alongside thrombocytopenia (25 × 10-9/L; normal range, 125-350×10-9/L). Bone marrow examinations revealed normal hematopoiesis. Because of the thrombocytopenia, chemotherapy was not given until the emerging of facial and neck edema. The second transthoracic echocardiography indicated that the mass progressed to the right atrium (RA) and superior vena cava (SVC) (Figure 2). After discussion with the patient’s families and the patient, we decided to give reduced dose of paclitaxel liposome (120 mg/m2). The patient’s symptoms deteriorated two weeks after the chemotherapy and died six weeks after the diagnosis of cardiac metastasis. Her families refused an autopsy.
We searched the literatures in PubMed between 1998 and 2018. Fifteen articles with 16 cases were included, which presented a clinical course and treatment of antemortem SCCUC-CM (Table 1) [1-15]. The mean age of initial diagnosis of cervical cancer was 49 years old but varied widely from 27 to 79 years old. The stage at which the patients were diagnosed also varied widely, ranging from stage I to IV. The pathologic type was all squamous cell carcinoma. The median duration from the first diagnosis to CM in the reported cases was 15 months. The median interval from diagnosis of CM to death was 5 months for patients treated with surgery and/or chemotherapy, 6 months for radiation and/or chemotherapy, and 1.5 months with thrombocytopenia. Two patients had the longest survival time for more than one year, because CM was solitary and aggressive treatment was arranged. As is known, there are four routes in Cardiac Metastasis (CM): (1) Retrograde lymphatic spreading, (2) Direct extension from the adjacent viscera, (3) Hematogenous spreading, and (4) Transvenous extension through the vena cava into the rightside chambers.
|Authors (Year)||Age of diagnosis of cervical||stage||Pathologic Type||Interval to cardiac metastasis||Clinical presentation||location||Primary treatment||treatment||Interval from cardiac metastasis||Solitary (yes or no)||diagnosis||thrombocytopenia||ECG||Overall survival (months)|
|Yang (2018)||46||IB1||squamous||68||Dypenia and chest pain||RV||S and adjuvant RT||Palliative treatment and C||1.5||no||Echocardiography, CT and PET/CT||yes||Flattened T-wave in leads III, aVL, aVF, V4-V6||70|
|Han (2017)||44||IV||squamous||0||Dypenia and chest pain||RV||S and C||S and C||15||yes||PET/ CT echocardiography and operation||NR||NR||15|
|Tsuchida (2016)||79||IB1||squamous||12||Epigastric discomfort and general malaise||RV||RT||Supportive treatment||1||yes||Transthoracic echocardiography, CT, MRI||Yes||Low voltage amplitudes in leads V1-V6 and T-wave inversion in leads V3-V6||13|
|Okamoto (2015)||27||IB1||squamous||15||asymptomatic||RV||S, C and RT||none||0.7 (21 days)||no||PET and CT||yes||NR||16|
|Schawkat (2014)||31||IIB||squamous||15||Dyspnea and feve||LV and RV||S and adjuvant CRT||C||NR||no||Transthoracic echocardiography, MRI and transcatheter biopsy||NR||ST-segment in V3-V6||NR|
|Byun (2013)||32||IIA2||squamous||15||Exertional dyspnea||RV and RA||S and adjuvant CRT||S and C||13||NR||Echocardiography, Chest CT and operation||NR||NR||32|
|Miller (2010)||48||IB2||squamous||48||Chet pain||Tricuspid valve and RA||CRT||C and RT||8||no||MRI and biopsy||NR||NR||56|
|Borsaru (2007)||42||IVB||squamous||6||Chest pain and respiratoty distress||RV and RA||RT||S||NR||NR||Echocardiography CT and operation||yes||NR||NR|
|Nakao (2006)||57||IIIB||squamous||10||Cough, chest pain and shortness of breath||RA||Concurrent CRT||S||2||no||Echocardiography and operation||NR||NR||12|
|Ferraz (2006)||63||NR||squamous||NR||Dyspnea and fatigue||RV||S, C and RT||S||More than 5||NR||Echocardiography and operation||NR||Area of inactivation in anterior wall and T wave inversion in leads V3 and V4||NR|
|Saitho (2005)||68||IIIB||squamous||15||Shortness of breath||RV||RT||S and C||5||yes||Echocardiography and Chest CT||NR||NR||20|
|Feys (2005)||37||IIIB||squamous||NR||Cough, fever and short of Breath and sweating||RV||RT and C||RT and C||More than 8||no||Echocardiography and PET/CT||NR||Sinus tachycardia, low voltage QRS and non-specific T-wave abnormalities||NR|
|Inamura (2004)||58||IB1||squamous||43||Chest pain, cough and dyspnea||RV||S and C||Palliative S||4||no||Echocardiography and CT||Yes||Low voltage amplitudes in limb and chest leads and an S||48|
|Iwaki (2001)||49||NR||squamous||0||Cough and low-grade fever||RV||/||CRT||2||no||Echocardiography and biopsy||yes||Sinus tachycardia, inverted T waves in leads V1 to V4 and low voltage in the limb leads||2|
|Harvey (2000)||44||IB1||squamous||6||asymptomatic||RV||RT||S and RT, C||More than 8||yes||Echocardiography and CT||NR||NR||More than 14|
|Lemus (1998)||53||IB||squamous||18||Dyspnea||RV||RT and S||CRT||1||no||Echocardiography and MRI||yes||NR||19|
|Lemus (1998)||48||IIIB||squamous||6||dyspnea||RV||RT||CRT||7||no||Echocardiography and MRI||yes||NR||13|
S: Surgery, C: Chemotherapy, RT: Radiotherapy, CRT: Radio-/Chemotherapy, NR: Not Report, RV: Right Ventricle, LV: Left Ventricle, RA: Right Atrium
After analyzing the images from transthoracic echocardiography in two time points with patient’s clinical manifestations, we considered that the carcinoma metastasized from the cervix to the right ventricle firstly. Due to the high pressure in the right ventricle and no effective treatment, it spreaded to the right atrium and superior vena cava. For most of the reported cases, the spreading route of these cervical carcinomas was hematogeneous through the cervical plexus, inferior vena cave (IVC) into right atrium, and finally the right ventricle . In Nakao’s study, they reported a patient with carcinoma of the uterine cervix developed metastatic tumors in the para-aortic lymph nodes and extended through the IVC into the RA .
Even though it was rare to see metastasis from para-aortic lymph nodes to the heart, the route was also in the way that the tumor extended into the IVC and growed into the right chamber. The right side of the heart was more commonly involved than the left side. Of the 17 cases including the current case, 16 occurred in the right side, one occurred in the right and the left side.
The possible reasons may include: (1) Direct seeding in the heart by microemboli from lymphatics and venous return, (2) The filtering of the pulmonary circulation, (3) The slower flow in the right chambers, and (4) The presence of pulmonary tumor emboli might decrease the right cardiac blood flow further, resulting in a more hospitable environment for tumor cell adherence to the endocardial wall.
Cardiac tumors are divided into primary and secondary tumors. Primary cardiac tumors are rare, and the incidence was 0.001–0.3% by autopsy, while metastatic tumors were reported to be 20 to 40 times more common by autopsy . For patients with known malignancy, the incidence of CM was 9% , and the risk of CM increased with a patient’s overall metastatic burden . Tumors with high rates of CM include lung cancers, breast cancers, hematologic malignancies and melanoma. Pleural mesothelioma and melanoma had an unusual proclivity to involve the heart, with an estimate of 28% to 56% of patients with metastatic melanoma having some cardiac involvement .
Of all the CM, intracavitary, endocardial, or valvular metastasis, such as the one described in our case, occurred less than 6%. Eighty percent of all these types of metastasis in cervical carcinoma occurred in the right chambers and rarely in the left chambers. The prognosis of a metastatic heart tumor was poor, the average survival time for patients with this diagnosis was less than six months.
The severity of clinical symptoms in patients with CM was variable and differed depending on the extent and the localization within the heart. Cardiac metastasis may cause medical emergencies or more often no early symptoms and remain unrecognized until the postmortem autopsy. Dyspnea, palpitations, syncope and chest pain are common clinical presentations of CM. Congestive heart failure, cardiac arrhythmia, heart block, acute myocardial infarction, myocardial rupture and systemic embolization are other lifethreatening manifestations of CM. Other clinical manifestations include symptoms of pericarditis, pericardial effusion, and constrictive pericarditis may happen if pericardium is involvement. Of all the cases listed in Table 1, the most common clinical manifestations were: Dyspnea 12/17 (71%) and chest pain 6/17 (35%), others included cough and fever. Cardiac metastasis should be suspected if patients with cervical carcinoma have such complaints, particularly with other distant metastases or thoracic involvement.
Physical examination is of vital importance to find various hints of CM such as new murmurs from intracardiac masses. ECG acts as a useful but nonspecific technique, abnormalities in ECG can remind us the possibility of CM. In our case, the ECG displayed flattened T-wave in leads III, aVL, aVF, V4-V6.
Non-invasive imaging plays a paramount role in investigating cardiac masses and establishing a diagnosis.
Most cardiac masses are initially detected by echocardiography which can offer information on the location, size, and mobility of cardiac masses. It was reported that the diagnostic accuracy of echocardiography was as high as 80% . Limitations of echocardiography include low image quality, limited visualization of the entire wall of the apex and base of the heart and extra-cardiac structure. Cardiac CT and cardiac magnetic resonance imaging (CMR) have superb spatial resolution and image quality which can provide additional non-invasive characterization of cardiac masses. Also, they visualize extra-cardiac structures which are helpful to identify direct tumor extension from adjacent mediastinal structures. The tissue characterization capabilities of CMR can be used to differentiate infiltrating metastasis from myocardium, and tumor from thrombus. PET-CT is a non-invasive imaging technique used to detect occult or distant metastasis at a relatively early stage and to further clarify the existing abnormal radiologic findings.
It was reported that even in an individual, the cardiac uptake of FDP by left ventricle differed from that of the right ventricle. This masking causes difficulty in detection of any cardiac mass or lesion . For intra-cardiac metastasis in the cervical carcinoma, characteristic on MRI are low signal intensity on T1-weighted imaging, high signal intensity on T2- weighted imaging and mostly enhance. Thrombi and primary cardiac tumors should be taken into consideration when give the diagnosis of intracardiac metastasis. For thrombi, the most common place is the left heart, and it is hypo-intensive in T1- and T2-weighted imaging and lacks internal enhancement .
In our case, decreased platelets and increased FDG and Ddimers were detected and impeded further effective treatment when CM was suspected. Bone marrow examination revealed normal hematopoiesis, so as the case reported by Kazuhiro Okamoto . It may be the result of the consumption and destruction of platelets as blood flowed through the damaged myocardium, as well as the consumption of platelets in hypercoagulable state induced by tumor embolization and multiple pulmonary emboli.
Among the 8 cases, including current case, in which thrombocytopenia was reported, the interval from CM to death was shorter than those without thrombocytopenia, seven cases were shorter than 2 months, and only one case was 7 months. Our patient was very similar to the second patient reported by Julio F. Lemus  and the patient reported by Kazuhiro Okamoto .
The difference was that the second patient reported by Julio F. Lemus received aggressive therapy (radiation therapy with total delivery of 6000 cGy to the heart concurrent with infusional 5-FU and cisplatin), thrombocytopenia was developed in the course of the therapy not prior to initiation of therapy. These may be the reason that this patient had a longer interval than other cases with thrombocytopenia. Considering all these information, we concluded the decreased platelets to be a negative prognostic factor for CM of cervical carcinoma.
Several studies recommended that aggressive treatment lengthened the patients’ survival time. Byun et al. reported a case of 32-year-old female diagnosed as cervical cancer (squamous cell carcinoma) stage IIA2 with exertional dyspnea which was the result of metastatic cardiac mass. The patient was treated with surgical excision followed by chemotherapy using paclitaxel and carboplatin.
The patient survived for 13 months after the diagnosis of CM . Han et al. reported a case of isolated intracavitary CM arising from squamous cell carcinoma of the cervix. The patient was treated with surgery followed by 12 cycles chemotherapy using paclitaxel and cisplatin. The patient died 14 months and 4 weeks after the diagnosis of CM . Radiotherapy can also be an option some literatures reported their experience in treating CM with radiation. Only two patients completed a total delivery of 6000 cGy to the heart.
The survival time for the two patients were 7 months and more than 8 months, respectively. Advances in computerguided imaging technology and radiation therapy planning technology enable radiation dose to reach the definitive dose to only the involved side of the heart, with no compromise to the other side of the heart. A total dose of 6000 cGy is recommended. Aggressive treatment includes surgical resection, radiotherapy and systemic chemotherapy, which may help to prolong the overall survival for solitary CM. Patients’ general conditions, should also be taken into consideration.
Patients with SCCUC should be carefully monitored and followed up. For patients diagnosed in advanced stage, cardiac evaluation should be included in follow-ups. It is important to suspect the diagnosis of CM in patients with repetitious increased D-Dimers and FDG, decreased platelets, and the complaint of dyspnea and chest pain. Echocardiography, cardiac CT and CMR are useful in the diagnosis of CM. The prognosis for CM is extremely poor, the survival time for most patients was less 1 year, and even shorter, about 2 months for the patients with thrombocytopenia. So far, there is no standard treatment for SCCUC-CM. Aggressive therapies may prolong survival time, including surgical intervention, chemotherapy and whole heart radiation therapy. It is of vital importance to follow up and examine the high-risk patients so that proper intervention could be made in the early stage, which may be the most effective way to prolong the survival time of cervical carcinoma patients with cardiac metastasis.
All Published work is licensed under a Creative Commons Attribution 4.0 International License
Copyright © 2019 All rights reserved. iMedPub LTD Last revised : August 18, 2019