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Ambiguous presentations of pulmonary epithelioid hemangioendothelioma: Two case reports of a rare pulmonary malignancy

机译:肺上皮样血管内皮瘤的模棱两可的表现:2例罕见的肺恶性肿瘤报告

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摘要

Pulmonary epithelioid hemangioendothelioma is an uncommon lung malignancy of endothelial origin. Besides demonstrating unpredictable presentation features and prognosis, the paucity of established treatment guidelines remains a challenge in managing these patients. We present two patients. The first patient presented with chronic productive cough over 1-year duration. He was initially diagnosed and showed partial response to treatment for cardiac failure. A persistent right upper zone consolidation on chest radiograph prompted further investigations which revealed the diagnosis of pulmonary epithelioid hemangioendothelioma. The second patient presented with right-sided hemiparesis for 1-month duration. Initial computer tomography scan of the brain showed findings of distant metastatic foci. Subsequent investigations revealed pulmonary epithelioid hemangioendothelioma as the primary lesion. Both patients succumbed without any treatment due to rapid progression of the disease. We believe that pulmonary epithelioid hemangioendothelioma is undoubtedly rarely reported in south-east Asia region. In these two case reports, the patients were diagnosed in west and east Malaysia, respectively, in the same year (2015). Both cases highlight the increasing prevalence of pulmonary epithelioid hemangioendothelioma. We postulate that this could possibly be secondary to the advancement in diagnostic capabilities and improved healthcare facilities available in this region. Late presentation of pulmonary epithelioid hemangioendothelioma generally results in grave prognosis. Further investigations are required to elucidate the nature of progression and therapeutic options for patients with pulmonary epithelioid hemangioendothelioma.
机译:肺上皮样血管内皮瘤是内皮源性肺恶性肿瘤。除了表现出无法预测的表现特征和预后外,建立治疗指南的缺乏仍然是管理这些患者的挑战。我们目前有两名患者。第一例患者出现慢性咳嗽超过1年。他最初被诊断出并表现出对心力衰竭治疗的部分反应。胸部X线照片上持续存在的右上区巩固提示了进一步的研究,这些发现揭示了肺上皮样血管内皮瘤的诊断。第二例患者出现右侧偏瘫,持续1个月。最初对大脑的计算机断层扫描扫描显示了远处转移灶的发现。随后的调查显示,肺上皮样血管内皮瘤是原发灶。由于疾病的快速发展,两名患者均未接受任何治疗而屈服。我们相信,在东南亚地区,肺上皮样血管内皮瘤无疑是很少报道的。在这两个病例报告中,同一年(2015年)分别在马来西亚西部和东部诊断出患者。这两种情况都突出了肺上皮样血管内皮瘤的患病率上升。我们推测,这可能是该地区诊断能力提高和医疗设施改善的次要条件。肺上皮样血管内皮瘤的晚期表现通常会导致严重的预后。需要进行进一步的研究以阐明肺上皮样血管内皮瘤患者的进展性质和治疗选择。

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