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脾脏血管瘤破裂:1 例报告及文献复习

Peliosis of the spleen as an unusual cause of splenic rupture: A case report and a review of literature.

机构信息

Department of Pathology, Faculty of Medicine, Pavol Jozef Šafárik University and Louis Pasteur University Hospital in Košice, Rastislavova 43, 040 01, Košice, Slovakia.

Forensic Medicine and Pathological Anatomy Workplace in Košice of Health Care Surveillance Authority, Ipeľská 1, 043 74, Košice, Slovakia.

出版信息

J Forensic Leg Med. 2024 Apr;103:102659. doi: 10.1016/j.jflm.2024.102659. Epub 2024 Feb 28.

DOI:10.1016/j.jflm.2024.102659
PMID:38431990
Abstract

Isolated splenic peliosis is an extremely rare condition characterized by the presence of multiple blood-filled cavities, occasionally resulting in non-traumatic splenic rupture with fatal bleeding. In our case, a 64-year-old man was brought by ambulance due to weakness and abdominal pain without nausea or febrility. On clinical examination, the patient was sensitive to palpation with significant tenderness over the abdomen but no associated features of peritonitis. He collapsed during the imaging examination and became unconscious and asystolic. Cardiopulmonary resuscitation was not successful. The patient died approximately within 2 hours of admission to the hospital. Postmortal examination showed 2800 ml of intraperitoneal blood with clots and a laceration of the lower pole of the spleen. Macroscopic examination of the spleen revealed huge nodular splenomegaly, measuring 21 cm x 19 cm x 5 cm, weighing 755 g. On the cut surfaces, multiple randomly distributed blood-filled cavities ranging from 0,5 to 2 cm in diameter were seen. At microscopic examination, the specimens showed multiple irregular haemorrhagic cyst-like lesions that were not lined by any epithelium or sinusoidal endothelium, consistent with the diagnosis of peliosis lienis. Although the condition is often clinically silent, the forensic pathological significance arises from the differential diagnosis of resultant intraperitoneal haemorrhage and sudden death, mimicking a violent death.

摘要

孤立性脾血管瘤病是一种极为罕见的疾病,其特征为存在多个充满血液的腔隙,偶尔导致非外伤性脾破裂并发生致命性出血。在我们的病例中,一名 64 岁男性因虚弱和腹痛而被救护车送来,无恶心或发热。临床检查时,患者腹部触诊敏感,有明显压痛,但无腹膜炎的相关特征。在影像学检查过程中,患者突然晕倒,意识丧失,心搏停止。心肺复苏未成功。患者大约在入院后 2 小时内死亡。尸检显示腹腔内有 2800 毫升血液和血块,以及脾脏下极的撕裂伤。脾脏的大体检查显示巨大的结节性脾肿大,大小为 21 厘米×19 厘米×5 厘米,重 755 克。在切面,可见多个直径 0.5 至 2 厘米的随机分布的充满血液的腔隙。显微镜下,标本显示多个不规则的出血性囊状病变,无任何上皮或窦状内皮细胞排列,符合肝血管瘤病的诊断。尽管该病症通常无临床症状,但法医学病理学意义在于源于导致的腹腔内出血和猝死的鉴别诊断,类似于暴力死亡。

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