An Infant Autopsy Case of Acute Appendicitis with Lymphoid Hyperplasia.

IF 1.4 Q3 PEDIATRICS
Momoka Tanabe, Kazuho Maeda, Hikaru Kuninaka, Moe Mukai, Noriko Ogawa, Ayako Nasu, Chiaki Fuke, Yosuke Usumoto, Yoko Ihama
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Abstract

Acute appendicitis is a common cause of acute abdominal pain but is rare in infants because of anatomical and physiological characteristics that reduce the risk of the luminal obstruction of the appendix. However, when it occurs in infants, it is often difficult to diagnose clinically and may progress rapidly to a fatal outcome. We report a forensic autopsy case of an 11-month-old infant who died 2 d after developing fever and decreased oral intake, without antemortem diagnosis. Autopsy revealed fibrinous ascitic fluid and an edematous, dark-red appendix with fibrin deposits, but no macroscopic luminal obstruction or perforation. Histopathological examination showed diffuse inflammatory cell infiltration and hemorrhage across all layers of the middle and peripheral portions of the appendix, along with lymphoid hyperplasia in the middle portion. Intestinal bacteria were detected in the ascitic fluid. The cause of death was identified as acute appendicitis with subsequent generalized peritonitis. Although luminal obstruction is a common cause of appendicitis, it was not observed macroscopically in this case. However, histopathological findings suggested that lymphoid hyperplasia in the middle portion of the appendix caused luminal narrowing and impaired circulation in the appendiceal wall, triggering appendicitis. This case demonstrates that infantile appendicitis can be fatal even without perforation and highlights the potential role of lymphoid hyperplasia in the pathogenesis. It also underscores the importance of considering appendicitis in the differential diagnosis of infants with nonspecific symptoms and illustrates the value of postmortem histopathological investigation in elucidating the disease mechanism.

婴儿急性阑尾炎伴淋巴样增生尸检1例。
急性阑尾炎是急性腹痛的常见原因,但在婴儿中很少见,因为其解剖和生理特征降低了阑尾腔梗阻的风险。然而,当它发生在婴儿时,通常难以临床诊断,并可能迅速发展到致命的结果。我们报告了一个11个月大的婴儿在发烧和口服摄入量减少后2天死亡的法医尸检病例,没有死前诊断。尸检发现纤维性腹水和肿胀的暗红色阑尾伴纤维蛋白沉积,但未见宏观腔梗阻或穿孔。组织病理学检查显示阑尾中部和周围各层弥漫性炎症细胞浸润和出血,中部淋巴样增生。腹水中检出肠道细菌。死亡原因被确定为急性阑尾炎并继发广泛性腹膜炎。虽然管腔梗阻是阑尾炎的常见原因,但在本病例中未观察到。然而,组织病理学结果提示阑尾中部淋巴样增生引起阑尾腔狭窄和阑尾壁循环受损,引发阑尾炎。本病例表明,即使没有穿孔,婴儿阑尾炎也可能是致命的,并强调了淋巴样增生在发病机制中的潜在作用。它还强调了考虑阑尾炎在婴儿非特异性症状鉴别诊断中的重要性,并说明了死后组织病理学调查在阐明疾病机制中的价值。
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来源期刊
Pediatric Reports
Pediatric Reports PEDIATRICS-
CiteScore
2.10
自引率
0.00%
发文量
55
审稿时长
11 weeks
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