A forensic case of abdominal cocoon syndrome

被引:1
|
作者
Stefano, Tambuzzi [1 ]
Guendalina, Gentile [1 ]
Michele, Boracchi [1 ]
Riccardo, Zoja [1 ]
Andrea, Gentilomo [2 ]
机构
[1] Univ Milan, Dipartimento Sci Biomed Salute, Sez Med Legale & Assicurazioni, Lab Istopatol Forense & Microbiol Med Legale, Via Luigi Mangiagalli 37, I-20133 Milan, Italy
[2] Univ Milan, Dipartimento Sci Giurid Cesare Beccaria, Via Festa Perdono 7, I-20122 Milan, Italy
关键词
Cocoon syndrome; Sclerosing encapsulating peritonitis; Peritoneal sclerosis; Autopsy; SCLEROSING ENCAPSULATING PERITONITIS; OBSTRUCTION; MANAGEMENT;
D O I
10.1007/s12024-022-00562-6
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
The term "cocoon syndrome " defines a sclerosing encapsulating peritonitis (SEP) that involves a chronic fibrotic inflammatory reaction of the parietal peritoneum and of the viscera leading to a complete sclerosis. The cocoon that is formed causes an incarceration of the intestinal loops with severe complications leading to high mortality. We are presenting the case of a 15-year-old young man that underwent surgery for appendectomy and that was evaluated for having a regular abdominal state. During the post-surgery period, however, several episodes of intestinal occlusion required further surgical interventions leading to a right hemicolectomy. The presence of a fibrotic-adhesive ligneous peritonitis with blended intestinal loops, severely thickened walls, and intestinal scaring stenosis was observed during his second surgical operation. A stenosis of the colostomy led to a worsening of the vital signs of the young man with the onset of a cardiac failure and subsequent decease. Macroscopic autopsy examination and histological analysis confirmed the severe obstructive adhesive encapsulating abdominal context allowing to trace back the cause of death to a cocoon syndrome. Since no predisposing factor could be found, we hypothesized that this case could be characterized by an excessive peritoneal reactivity due to surgical appendectomy. Cocoon syndrome is a rare pathology, and its microscopic features are seldomly observed and could be underestimated. We present a directly observed case with a very substantial macroscopic and microscopic context.
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页码:273 / 279
页数:7
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