Gitto Lorenzo, Richardson Timothy E, Serinelli Serenella, Diana Francesco, Peschillo Simone, Domenicucci Maurizio
Department of Pathology, State University of New York - Upstate Medical University, 750 E Adams St, Syracuse, NY, 13210, USA.
Department of Pathology, Neuropathology Laboratory, State University of New York - Upstate Medical University, 750 E. Adam St, Syracuse, NY, 13210, USA.
Forensic Sci Med Pathol. 2019 Sep;15(3):474-480. doi: 10.1007/s12024-019-00122-5. Epub 2019 Jun 19.
Intracranial pseudoaneurysm (IPA) is a rare but likely underdiagnosed cause of intracranial hemorrhage, which accounts for just 1-6% of all intracranial aneurysms. Spontaneous IPAs are exceptionally rare, and their etiology and features are not well defined. Herein, we report a case of a pediatric patient who died from massive intracranial bleeding due to the rupture of a spontaneous IPA after undergoing multiple radiological studies and neurosurgical operations. At the postmortem examination of the brain, a giant size pseudoaneurysm of the right middle cerebral artery was observed. Microscopic examination demonstrated variable wall thickness and dense fibrosis focally in the vessel wall with disruption of the media structure together with a loss and fragmentation of the elastic laminae, loss of organization of smooth muscle cells in the media, and multifocal areas of hemorrhage throughout the vessel wall, as well as direct evidence of wall dissection. Since IPAs without any traumatic or infective history are extremely uncommon, further pathologic studies should be performed to clarify spontaneous pseudoaneurysm etiology.
颅内假性动脉瘤(IPA)是一种罕见但可能未被充分诊断的颅内出血原因,仅占所有颅内动脉瘤的1%至6%。自发性IPA极为罕见,其病因和特征尚不明确。在此,我们报告一例儿科患者,该患者在接受多次放射学检查和神经外科手术后,因自发性IPA破裂导致大量颅内出血死亡。在脑部尸检时,观察到右大脑中动脉有一个巨大的假性动脉瘤。显微镜检查显示血管壁厚度不一,局部有致密纤维化,中层结构破坏,弹性膜缺失和断裂,中层平滑肌细胞排列紊乱,血管壁多处出血,以及壁内夹层的直接证据。由于无任何创伤或感染史的IPA极为罕见,应进行进一步的病理研究以阐明自发性假性动脉瘤的病因。