Marques Mendes Edite, Ferreira António, Felgueiras Paula, Silva Augusta, Ribeiro Carlos, Guerra Diana, de Melo Daniel Pereira, Manuel Lopes José
Departamento de Medicina, Medicina 1, Unidade Local de Saúde do Alto Minho, Hospital SantaLuzia, Viana do Castelo,Portugal.
Departamento de Anatomia Patológica, Centro Hospitalar de S.João, Porto, Portugal.
Oxf Med Case Reports. 2017 Jul 5;2017(7):omx031. doi: 10.1093/omcr/omx031. eCollection 2017 Jul.
Intimal (spindle-cell) sarcomas are exceptionally rare and are highly aggressive cardiac tumors. The authors describe a case of a 43-year-old female, presenting with a 3-month history of constitutional symptoms with fever, night sweats, anorexia and weight loss, associated with productive cough and pleural effusion that was admitted with clinical suspicion of pulmonary tuberculosis. The patient developed sudden acute heart failure symptoms during hospitalization, leading to mechanical ventilation. Computed tomography scan with contrast showed a cardiac tumor filling the left atrium causing compression of pulmonary veins. Surgical resection was performed and histologic examination revealed an intimal sarcoma. Although commenced on adjuvant chemotherapy, local tumor recurrence occurred with pericardium invasion. The patient died within 4 months of initial diagnosis. This report aims to describe an unusual presentation of this rare disease entity, and to discuss its highly aggressive clinical course.
内膜(梭形细胞)肉瘤极为罕见,是具有高度侵袭性的心脏肿瘤。作者描述了一例43岁女性病例,该患者有3个月的全身症状病史,包括发热、盗汗、厌食和体重减轻,伴有咳痰和胸腔积液,因临床怀疑肺结核入院。患者在住院期间突然出现急性心力衰竭症状,导致机械通气。增强计算机断层扫描显示心脏肿瘤充满左心房,压迫肺静脉。进行了手术切除,组织学检查显示为内膜肉瘤。尽管开始了辅助化疗,但仍发生了局部肿瘤复发并侵犯心包。患者在初次诊断后4个月内死亡。本报告旨在描述这种罕见疾病实体的不寻常表现,并讨论其高度侵袭性的临床病程。