Zhao Shuquan, Zhu Longlong, Tong Fang, Tinzin Lopsong, Huang Fang, Zhou Yiwu
Department of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, No. 13 Hangkong Road, Wuhan 430030, PR China.
Department of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, No. 13 Hangkong Road, Wuhan 430030, PR China.
Leg Med (Tokyo). 2020 Nov;47:101785. doi: 10.1016/j.legalmed.2020.101785. Epub 2020 Sep 8.
Splenic angiosarcoma (SA) is a rare disease that can cause spontaneous splenic rupture leading to unexpected death. The rare incidence and non-specific clinical presentations made the early correct diagnosis of SA impossible in clinical practice. Even with medical intervention, 80% of patients died within 6 months after diagnosis. Here, we report a man who had complained of abdominal distension for 2 weeks and succumbed to the disease nine hours after admission. Diagnosis of hepatic and splenic angiosarcomas was based on post-mortem histopathological examination and immunohistochemistry, and the cause of death was hemorrhagic shock caused by spontaneous splenic rupture secondary to SA. This present case was the first forensic autopsy of spontaneous splenic rupture secondary to SA, which can highlight the diagnosis of rare diseases in forensic practice, and forensic pathologists should bear in mind these rare diseases even in routine practice.
脾血管肉瘤(SA)是一种罕见疾病,可导致自发性脾破裂,进而引发意外死亡。其罕见的发病率和非特异性临床表现使得在临床实践中早期准确诊断SA成为不可能。即便进行医学干预,80%的患者在确诊后6个月内死亡。在此,我们报告一名男性,他主诉腹胀2周,入院9小时后死于该病。肝脾血管肉瘤的诊断基于尸检组织病理学检查和免疫组化,死亡原因是SA继发自发性脾破裂导致的失血性休克。本病例是首例SA继发自发性脾破裂的法医尸检,这可凸显法医实践中罕见疾病的诊断,即使在常规实践中法医病理学家也应牢记这些罕见疾病。