偶然发现原发性心脏平滑肌肉瘤起源于右心房的25岁男性。病例报告

Anna Katrina M. Donato, Felipe, Jr. S. Templo
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摘要

背景:原发性心脏肿瘤极为罕见,占所有记录在案的心脏肿瘤的不到1%,其中大多数是良性的。在原发性恶性心脏肿瘤中,平滑肌肉瘤仅占所有文献病例的1%,它通常累及左心房。我们报告一例罕见的原发性心脏平滑肌肉瘤起源于右心房的25岁男性。病例:患者是一名25岁的菲律宾男性,在2d超声心动图上表现为进行性呼吸困难,直立呼吸,房间隔处有一个大的,异质的卵形肿块,最宽尺寸为7.0 cm x 3.16cm。患者最终接受了右心房肿块的紧急切除。术后,患者不能耐受手术,最终在心肺复苏后死亡。组织病理表现:纤维黏液样间质中,显微镜切片显示一个纺锤状细胞肿瘤,具有不规则的束状和轮状结构,其间散布着炎症细胞。梭形细胞呈多形性,细胞核深染,部分核仁突出,胞浆嗜酸性。可见有丝分裂象、坏死区域和出血。免疫组化研究显示肿瘤细胞对平滑肌肌动蛋白(SMA)和Vimentin具有反应性。马森氏三色染色也是阳性的。S100、Myogenin和Desmin无反应。Ki-67和p53的增殖指数为15-20%。结论:原发性心脏平滑肌肉瘤是一种极为罕见的肿瘤,在所有记录的原发性心脏恶性肿瘤中发生率不到1%。从其他部位转移更为常见。它具有侵袭性临床病程和预后差,其特征与其他软组织肿瘤重叠。因此,应采用额外的免疫组织化学研究和特殊染色来获得明确的诊断,以便为受影响的患者提供适当的管理和干预。
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Incidental finding of a primary cardiac leiomyosarcoma originating from the right atrium of a 25-year old male. A Case Report
BACKGROUND: Primary cardiac tumors are extremely rare and encompass less than 1% of all documented cardiac neoplasms with a majority of these being benign. Among the malignant primary cardiac tumors, leiomyosarcoma accounts for only 1% all documented cases and it commonly involves the left atrium. We present a rare case of a primary cardiac leiomyosarcoma originating from the right atrium of a 25-year-old male.CASE: The patient was a 25-year-old Filipino male who presented with progressive dyspnea, orthopnea, and a large, heterogenous, ovoid mass attached at the atrial septum measuring 7.0 cm x 3.16cm in widest dimension on 2D-echocardiography. The patient eventually underwent emergency excision of the right atrial mass. Post-operatively, the patient did not tolerate the procedure and ultimately expired after attempts of cardiopulmonary resuscitation.HISTOPATHOLOGIC FINDINGS: Microscopic sections show a spindle-cell neoplasm with irregular fascicles and whorled configurations interspersed with inflammatory cells in a fibromyxoid stroma. The spindle cells showed pleomorphic, hyperchromatic nuclei, some with prominent nucleoli and eosinophilic cytoplasm. Mitotic figures, areas of necrosis, and hemorrhages are seen. Immunohistochemical studies show reactivity of the neoplastic cells to Smooth Muscle Actin (SMA) and Vimentin. Masson’s Trichrome Stain is also positive. S100, Myogenin, and Desmin show non-reactivity. Proliferation index is at 15-20% using Ki-67 and p53.CONCLUSION: Primary cardiac leiomyosarcoma is an extremely rare tumor occurring in less than 1% of all documented primary malignant cardiac neoplasms. Metastases originating from other sites are more common. It has an aggressive clinical course and a dismal prognosis with features overlapping that of other soft tissue neoplasms. Hence, additional immunohistochemical studies and special stains should be employed to arrive with a definitive diagnosis so that appropriate management and intervention may be offered to affected patients.
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