1型神经纤维瘤病合并未确诊嗜铬细胞瘤患者的自发性血胸。
Spontaneous hemothorax in a patient with neurofibromatosis type 1 and undiagnosed pheochromocytoma.
作者信息
Conlon Niamh P, Redmond Karen C, Celi Leo A
机构信息
Department of Anesthesia and Intensive Care, Mater Misericordiae University Hospital, Dublin, Ireland.
出版信息
Ann Thorac Surg. 2007 Sep;84(3):1021-3. doi: 10.1016/j.athoracsur.2007.04.024.
Abstract
Spontaneous hemothorax in neurofibromatosis type 1 rarely occurs, is potentially life-threatening, and requires expedient management. We present a case of massive hemothorax in a patient with neurofibromatosis type 1 caused by spontaneous rupture of the right internal mammary artery. A subsequently diagnosed underlying pheochromocytoma may be implicated in rupture of the arterial wall.
摘要
1型神经纤维瘤病患者自发性血胸很少见，有潜在生命危险，需要及时处理。我们报告一例1型神经纤维瘤病患者因右乳内动脉自发性破裂导致大量血胸的病例。随后诊断出的潜在嗜铬细胞瘤可能与动脉壁破裂有关。
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