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首页> 外文期刊>The Canadian journal of cardiology >Myxoid leiomyosarcoma of the left atrium: a rare malignancy of the heart and its comparison with atrial myxoma.
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Myxoid leiomyosarcoma of the left atrium: a rare malignancy of the heart and its comparison with atrial myxoma.

机译:左房粘液性平滑肌肉肉瘤:一种罕见的心脏恶性肿瘤,与房性粘液瘤比较。

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摘要

Primary tumours of the heart are rare. The majority of these tumours are benign, with myxomas located in the left atrium being the most common form. Almost all malignant tumours are sarcomas and occur preferentially in the right side of the heart. An exception to this rule is leiomyosarcoma, a rare form of primary cardiac sarcoma that occurs predominantly in the left atrium, as does cardiac myxoma. The case of a 53-year-old woman who presented with symptoms of mitral valve stenosis and pulmonary hypertension is reported. Cardiac catheterization, angiography and echocardiography revealed a left atrial mass that was interpreted as atrial myxoma. At the time of operation, the myxoid appearance of the tumour mass further supported this assumption. The tumour, including a wide rim of atrial septum, was removed with cautery. Histopathological examination unexpectedly showed that the tumour was not an atrial myxoma but rather a myxoid variant of a primary leiomyosarcoma. Immunohistochemistry and electron microscopy confirmed the diagnosis. Local radiotherapy was considered but deemed contraindicated in view of the longstanding pulmonary hypertension. Two months after excision, a repeat echocardiogram indicated recurrence of tumour in the left atrium, and the patient died a few days later. The preferential left atrial location and the frequently myxoid appearance of primary leiomyosarcomas of the heart make it particularly difficult to differentiate them preoperatively from atrial myxomas. The authors recommend resection of all atrial myxoid tumours with a wide (at least 1 cm) margin, combined with intraoperative frozen section diagnosis, because complete surgical resection appears to correlate with prolonged survival in the few reported cases of atrial leiomyosarcomas. In cases of incomplete initial resection or local recurrence in the absence of metastatic disease, heart transplantation may be a valid option in appropriately selected patients.
机译:心脏的原发性肿瘤很少见。这些肿瘤大多数是良性的,位于左心房的粘液瘤是最常见的形式。几乎所有恶性肿瘤都是肉瘤,优先发生在心脏的右侧。该规则的一个例外是平滑肌肉瘤,这是一种罕见的原发性心脏肉瘤,主要发生在左心房,而心脏粘液瘤也是如此。据报道,一例53岁的妇女出现二尖瓣狭窄和肺动脉高压的症状。心脏导管检查,血管造影和超声心动图检查发现左心房肿块被解释为心房粘液瘤。在手术时,肿瘤块的粘液样外观进一步支持了这一假设。烧灼除去包括房间隔宽缘在内的肿瘤。组织病理学检查意外地表明,该肿瘤不是房性粘液瘤,而是原发性平滑肌肉瘤的粘液样变体。免疫组织化学和电子显微镜证实了诊断。考虑到局部放疗,但考虑到长期存在的肺动脉高压,因此认为是禁忌的。切除后两个月,重复的超声心动图显示左心房肿瘤复发,患者在几天后死亡。优先的左心房位置和心脏原发性平滑肌肉瘤的频繁粘液样外观使得在术前将它们与心房粘液瘤区分开来特别困难。作者建议切除所有宽阔(至少1 cm)边缘的房性粘液样肿瘤,并结合术中冰冻切片诊断,因为在少数报道的房性平滑肌肉瘤病例中,完全的手术切除似乎与生存期延长相关。如果最初的切除不完全或没有转移性疾病的局部复发,在适当选择的患者中,心脏移植可能是有效的选择。

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