General Medicine, Hospitalization Service, Fundación Valle del Lili, Carrera 98 #18-49, 760032, Cali, Colombia.
Department of Internal Medicine, Fundación Valle del Lili, Carrera 98 #18-49, 760032, Cali, Colombia.
J Med Case Rep. 2020 Nov 23;14(1):228. doi: 10.1186/s13256-020-02562-y.
Osteosarcoma is a malignant tumor of the bone. The giant cell-rich osteosarcoma (GCRO) is a rare histological variant of the conventional osteosarcoma, accounting for 3% of all osteosarcomas. It has a variable clinical presentation, ranging from asymptomatic to multiple pathological fractures, mainly involving long bones, and less frequently the axial skeleton and soft tissues.
We present the case of a 25-year-old Hispanic woman, previously healthy, with a 1-month history of dyspnea on exertion, intermittent dry cough, hyporexia, and intermittent unquantified fever. She presented to the emergency department with a sudden increase in dyspnea during which she quickly entered ventilatory failure and cardiorespiratory arrest with pulseless electrical activity. Resuscitation maneuvers and orotracheal intubation were initiated, but effective ventilation was not achieved despite intubation and she was transferred to the intensive care unit of our institution. The chest radiograph showed a mediastinal mass that occluded and displaced the airway. The chest tomography showed a large mediastinal mass that involved the pleura and vertebral bodies. A thoracoscopic biopsy was performed that documented a conventional giant cell-rich osteosarcoma. The patient was considered to be inoperable due to the size and extent of the tumor and subsequently died.
The giant cell-rich osteosarcoma is a very rare histological variant of conventional osteosarcoma. Few cases of this type of osteosarcoma originating from the spine have been reported in the literature, and to our knowledge none of the reported cases included invasion to the chest cavity with airway compression and fatal acute respiratory failure that was present our case. Radiological and histological features of the GCRO must be taken into account to make a prompt diagnosis.
骨肉瘤是一种骨的恶性肿瘤。富含巨细胞的骨肉瘤(GCRO)是一种罕见的常规骨肉瘤组织学变体,占所有骨肉瘤的 3%。它的临床表现多变,从无症状到多发性病理性骨折不等,主要累及长骨,较少累及轴骨和软组织。
我们报告了一例 25 岁的西班牙裔女性,既往健康,1 个月前出现活动时呼吸困难、间歇性干咳、食欲减退和间歇性无法量化的发热。她因呼吸困难突然加重而就诊于急诊,在此期间她迅速出现通气衰竭和心搏骤停伴无脉电活动。进行了复苏操作和经口气管插管,但尽管进行了插管仍未实现有效通气,她被转至我们机构的重症监护病房。胸部 X 线片显示纵隔肿块导致气道阻塞和移位。胸部 CT 显示纵隔内有一个大肿块,累及胸膜和椎体。进行了胸腔镜活检,证实为常规富含巨细胞的骨肉瘤。由于肿瘤的大小和范围,患者被认为无法手术,随后死亡。
富含巨细胞的骨肉瘤是一种非常罕见的常规骨肉瘤组织学变体。文献中报道了少数几例源自脊柱的此类骨肉瘤病例,据我们所知,在报道的病例中没有一例包括侵犯胸腔并导致气道压迫和致命性急性呼吸衰竭,而这在我们的病例中存在。必须考虑 GCRO 的放射学和组织学特征以做出快速诊断。