Imaging Findings of a Primary Cardiac Osteosarcoma Arising From the Left Atrium and Mitral Posterior Leaflet with Multiple Metastases in A 58-Year-Old Woman

authors:

avatar Eun Jee Song 1 , avatar Se Hwan Kwon 2 , * , avatar Hyo Chul Youn 3 , avatar Soo Cheol Kim 3 , avatar Jong Soo Shin 4 , avatar Joo Hyeong Oh 2

Department of Medicine, Graduate School, Kyung Hee University, Seoul, Republic of Korea
Department of Radiology, College of Medicine, Kyung Hee University Hospital, Kyung Hee University, Seoul, Republic of Korea
Department of Cardiothoracic Surgery, College of Medicine, Kyung Hee University, Seoul, Republic of Korea
Department of Radiology, Kyung Hee University Hospital at Gangdong, Seoul, Republic of Korea

how to cite: Song E J, Kwon S H, Youn H C, Kim S C, Shin J S, et al. Imaging Findings of a Primary Cardiac Osteosarcoma Arising From the Left Atrium and Mitral Posterior Leaflet with Multiple Metastases in A 58-Year-Old Woman. I J Radiol. 2017;14(2):e31757. https://doi.org/10.5812/iranjradiol.31757.

Abstract

Primary cardiac osteosarcoma is a very rare malignancy with nonspecific symptoms, making early diagnosis a challenge. We report the computed tomography and magnetic resonance imaging findings of a primary cardiac osteosarcoma arising from the left atrium and posterior mitral leaflet in a 58-year-old woman with multiple metastases to the brain, skull, clavicle, lung, ribs, liver, lymph nodes, and thyroid gland.

1. Introduction

Primary cardiac tumors are found in 0.002% - 0.3% of patients in autopsy studies (1). A primary cardiac osteosarcoma is a clinical and pathological surprise, accounting for less than 10% of primary cardiac malignancies and only 3% - 9% of all cardiac sarcomas (1, 2). Unlike metastatic osteosarcoma, which most often occurs in the right atrium, primary cardiac osteosarcomas arise in the left atrium (LA) in the overwhelming majority of cases (2). We describe the computed tomography (CT) and magnetic resonance imaging (MRI) findings of a primary cardiac osteosarcoma arising from the LA and posterior mitral leaflet in a 58-year-old woman with multiple metastases to the brain, skull, clavicle, lung, ribs, liver, lymph nodes, and thyroid gland.

2. Case Presentation

A 58-year-old woman was admitted to our hospital complaining of chest discomfort, dyspnea, hoarseness, and a mild headache. Her symptoms had begun one month earlier. The patient denied a history of systemic disease, and her family history, including for malignancy, was non-contributory. An electrocardiogram (ECG) showed a sinus rhythm of 70 bpm, and all laboratory findings were within normal limits. A chest x-ray revealed clear lungs with a normal-sized heart. A transthoracic echocardiogram showed a 1.5 × 1.8 cm echogenic mass in the lateral wall of the LA adjacent to the posterior leaflet of the mitral valve (not shown).

For further evaluation, cardiac CT was performed using an ECG-gated 128-slice multi-detector CT scanner (Ingenuity; Philips Medical Systems, Best, the Netherlands). Unenhanced CT of the heart showed dense calcification in the tumor, and the contrast-enhanced mid-diastolic phase images showed a broad-based low-attenuation mass in the lateral wall of the LA adjacent to the mitral valve (Figure 1). CT also revealed diffuse thickening of the LA wall around the mass and the posterior leaflet of the mitral valve. No pleural effusion or lymph node enlargement was noted. MRI (Intera Achieva 3T; Philips Medical Systems, Best, the Netherlands) showed a lobulated mass with a broad stalk at the lateral wall of the LA, and diffuse thickening of the adjacent LA wall and posterior leaflet of the mitral valve. The mass was isointense relative to cardiac muscle on T1-weighted images (T1WI), and was hyperintense on T2-weighted images (T2WI) (Figure 2). The mass showed strong enhancement on the contrast-enhanced images.

Unenhanced (A) and contrast-enhanced (B) mid-diastolic-phase CT images showing a broad-based tumor (arrows) with dense calcification involving the LA lateral wall, with diffuse thickening of the surrounding LA wall and posterior leaflet of the mitral valve.
Unenhanced (A) and contrast-enhanced (B) mid-diastolic-phase CT images showing a broad-based tumor (arrows) with dense calcification involving the LA lateral wall, with diffuse thickening of the surrounding LA wall and posterior leaflet of the mitral valve.
MRI showing a lobulated, broad-based mass (arrows) at the lateral wall of the LA, and diffuse thickening of the surrounding LA wall and posterior leaflet of mitral valve. The mass was isointense relative to cardiac muscle on T1WI (A) and hyperintense on T2WI (B). On the contrast-enhanced images (C), the mass showed strong enhancement.
MRI showing a lobulated, broad-based mass (arrows) at the lateral wall of the LA, and diffuse thickening of the surrounding LA wall and posterior leaflet of mitral valve. The mass was isointense relative to cardiac muscle on T1WI (A) and hyperintense on T2WI (B). On the contrast-enhanced images (C), the mass showed strong enhancement.

An initial diagnosis of atrial myxoma was considered. However, the wall thickening that included the posterior mitral leaflet, along with the calcifications, made us consider other malignant cardiac tumors, such as metastasis or sarcoma. After a general evaluation, we decided to respect the tumor. Intraoperatively, the tumor was seen to have invaded the lateral wall of the LA and the posterior mitral leaflet (Figure 3). The atrial mass was resected, but complete resection and mitral valve replacement could not be performed due to tumor extension into the adjacent structures. Histologically, the LA mass was composed mainly of atypical spindle-shaped cells forming lace-like osteoid (Figure 4). The final diagnosis was primary cardiac osteosarcoma.

Intraoperative image showing the broad-based LA mass (arrow) with diffuse thickening of the surrounding LA wall and posterior leaflet of the mitral valve.
Intraoperative image showing the broad-based LA mass (arrow) with diffuse thickening of the surrounding LA wall and posterior leaflet of the mitral valve.
Microscopic image showing atypical round and spindle-shaped cells forming lace-like osteoid
Microscopic image showing atypical round and spindle-shaped cells forming lace-like osteoid

At that time, expansile osteolytic masses in the parietal bone were found on brain CT, measuring 2.0 × 2.0 cm (right) and 4.0 × 3.3 cm (left). A craniectomy and mass removal was performed, which confirmed metastatic osteosarcoma. The patient began chemotherapy with ifosfamide and doxorubicin. However, one year later, she presented with multiple metastases, including in the brain, skull, clavicle, lung, ribs, liver, lymph nodes, and thyroid gland. Positron emission tomography (PET)-CT showed multiple fluorodeoxyglucose (FDG)-avid areas in the metastatic lesions (Figure 5). At that time, the patient was admitted to the hospital for supportive care.

PET-CT image taken one year after surgery, showing multiple FDG-avid areas in the metastatic lesions (arrows).
PET-CT image taken one year after surgery, showing multiple FDG-avid areas in the metastatic lesions (arrows).

3. Discussion

Primary cardiac malignancies are rare, and most cardiac tumors are metastases, which are 20 - 40 fold more common than primary tumors (1, 2). Benign tumors, such as myxomas, lipomas, and papillary fibroelastomas, comprise approximately 75% of all primary cardiac tumors, while primary malignant tumors comprise approximately 25%. Primary cardiac osteosarcoma is rare, accounting for less than 10% of primary cardiac malignancies (1).

Primary cardiac osteosarcomas are commonly situated in the LA and are frequently confused with LA myxomas on imaging. Possible clinical presentations are similar to those of other mass lesions in the cardiac chambers and may be obstructive, embolic, or metastatic (3). The clinical manifestations of cardiac tumors depend on their anatomical location and reflect the degree of obstruction, invasion, and embolization of specific intracardiac structures. Most patients present with dyspnea secondary to mitral valve obstruction (3, 4). Our patient presented with chest discomfort, dyspnea, hoarseness, and a mild headache. In our case, there was debate over whether the cardiac lesion was a primary malignancy, metastatic tumor, or myxoma. Most reported cases of metastatic osteosarcoma are located in the right atrium, and primary osteosarcomas are found in the LA in the overwhelming majority of cases (2). Therefore, the cardiac lesion in our case was thought to be a primary cardiac tumor rather than metastasis. In addition, imaging findings such as a broad base of attachment and an infiltration pattern suggested primary cardiac malignancy rather than benign myxoma (5).

Primary cardiac osteosarcomas are very aggressive, with a high rate of recurrence and metastasis. Metastases are commonly observed at various sites at the time of the initial diagnosis, and the average survival is 6 months from the time of diagnosis (1, 3, 6). Metastases to distant organs, including the skin, brain, thyroid, lung, stomach, liver, kidney, muscle, intestine, peritoneum, and bone have been reported (4). Our case also revealed multiple metastases in the brain, skull, clavicle, lung, ribs, liver, lymph nodes, and thyroid gland, even though the patient had undergone chemotherapy after surgical removal of the tumor.

According to previous reports, the characteristic CT findings of cardiac osteosarcoma are a low-attenuation mass with dense calcification and a broad base of attachment (6). An aggressive growth pattern may be seen, such as extension or invasion into the surrounding structures (mitral valve, pulmonary veins, atrial septum, and epicardium) (1, 2). However, calcification may also be minimal, and in the early stages it may be mistaken as benign, including degenerative calcification of the mitral valve, caseous calcification of the mitral valve annulus, or another benign, dystrophic type of calcification (2). Our case showed relatively typical CT findings of osteosarcoma, including a densely calcified low-attenuation mass with diffuse thickening of the surrounding LA wall and posterior mitral leaflet.

The MRI characteristics of cardiac osteosarcomas still remain unclear. Yamagishi et al. (5) first reported the MRI findings of a cardiac osteosarcoma in which the tumor appeared as a huge mass of heterogeneous signal intensity in the LA. However, their report focused on the role of MRI in differentiating malignant from benign tumors. Cardiac osteosarcomas have been reported as irregularly lobulated masses with variable heterogeneous signal intensity on T1WI and heterogeneous hyperintensity on T2WI (1, 7). Ahn et al. (1) reported that cardiac osteosarcomas showed mildly heterogeneous high signal intensity on T1WI and heterogeneously high signal intensity on T2WI, with heterogeneous enhancement. Foci of hemorrhage may be seen as focal areas of high signal intensity on T1WI, whereas cystic or necrotic changes cause high signal intensity on T2WI. However, hemorrhage and necrosis may be seen on MRI in other sarcomas, making these findings nonspecific (7). In our case, the tumor showed isointense signal relative to cardiac muscle on T1WI, and heterogeneously hyperintense signal on T2WI, with relatively homogeneous enhancement on contrast-enhanced images. Further studies are needed to correlate the signal intensities on MRI images and the contrast-enhancement patterns on CT with the histological composition.

Due to its low incidence, no standard treatment for primary cardiac osteosarcoma has yet been established. Surgical resection is usually the initial treatment. Complete surgical excision is important for improving the survival rate and prognosis of patients with primary cardiac sarcoma (8, 9). Unfortunately, in our case, the tumor was not resected completely because it had extended into adjacent structures, including the LA wall and the posterior mitral valve leaflet. As a result, our patient developed multiple metastases despite undergoing chemotherapy.

In summary, we present the CT and MRI findings of a rare case of primary cardiac osteosarcoma arising from the LA and posterior mitral leaflet in a 58-year-old woman with multiple metastases to the brain, skull, clavicle, lung, ribs, liver, lymph nodes, and thyroid gland.

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