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两例因重复囊肿导致腹腔内动脉出血的婴儿病例:病例报告

Two infant cases of intraperitoneal arterial hemorrhage due to a duplication cyst: a case report.

作者信息

Fukazawa Hiroaki, Kajihara Keisuke, Kuroda Yasuhiro, Fujieda Yuki, Uemura Kotaro, Takeuchi Yuki, Samejima Yoshitomo, Kawahara Insu, Morita Keiichi, Iwade Tamaki, Maeda Kosaku

机构信息

Division of Pediatric Surgery, Department of Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.

Department of Pediatric Surgery, Kobe Children's Hospital, 1-6-7 Minatojima-minami, Chuo-ku, Kobe, 650-0047, Japan.

出版信息

Surg Case Rep. 2020 Mar 21;6(1):55. doi: 10.1186/s40792-020-00820-1.

Abstract

BACKGROUND

Intraperitoneal arterial hemorrhage without trauma is extremely rare. We report two infant cases of intraperitoneal arterial hemorrhage due to intestinal duplication.

CASE PRESENTATION

In case 1, a 2-month-old girl experienced sudden intraperitoneal hemorrhage from the middle colic artery with no apparent trauma. Hemostasis was achieved with suturing of the hemorrhage point, but the cause of hemorrhage was still unknown. Computed tomography after the first operation revealed a duodenal duplication cyst and a pseudopancreatic cyst. Percutaneous drainage of the pseudopancreatic cyst was performed, and the contents had high pancreatic amylase. As the size of the duodenal duplication cyst also decreased with this drainage, we suspected that the duodenal duplication cyst was connected to the pseudopancreatic cyst and the arterial hemorrhage. We hypothesized that the pancreatic juice inside the duplication cyst leaked into the intraperitoneal cavity and caused rupture of the arterial wall. Therefore, marsupialization of the duodenal duplication was performed to evacuate the pancreatic juice contained in the cyst toward the native duodenum. The postoperative course was uneventful. In case 2, a 6-month-old boy experienced sudden intraperitoneal hemorrhage without trauma. The hemorrhage site was identified as the ileocecal artery, and hemostasis was achieved with sutures. Tissue near the hemorrhage point was biopsied, because the cause of arterial wall rupture was still unknown. The biopsied tissue was found to be intestinal mucosa. The patient had recurrent abdominal pain after the first operation, and computed tomography showed a duplication cyst located near the hemorrhage point. Therefore, we resected the intestinal duplication. Pathology results showed that the intestinal duplication contained intestinal mucosa, ectopic gastric mucosa, and pancreatic tissue. The postoperative course was uneventful.

CONCLUSION

Intraperitoneal arterial hemorrhage without trauma is an extremely rare condition, and identifying its cause is difficult. To our knowledge, this is the first report of intraperitoneal arterial hemorrhage due to intestinal duplication. In cases of unexplained intraperitoneal arterial hemorrhage in infants, intestinal duplication near the hemorrhage point should be suspected.

摘要

背景

无创伤性的腹腔内动脉出血极为罕见。我们报告两例因肠重复畸形导致腹腔内动脉出血的婴儿病例。

病例介绍

病例1,一名2个月大的女孩在无明显创伤的情况下,出现了来自中结肠动脉的突发性腹腔内出血。通过缝合出血点实现了止血,但出血原因仍不明。首次手术后的计算机断层扫描显示十二指肠重复囊肿和假性胰腺囊肿。对假性胰腺囊肿进行了经皮引流,引流液中胰淀粉酶含量很高。随着引流,十二指肠重复囊肿的大小也减小了,我们怀疑十二指肠重复囊肿与假性胰腺囊肿及动脉出血有关。我们推测重复囊肿内的胰液漏入腹腔并导致动脉壁破裂。因此,对十二指肠重复囊肿进行了袋形缝合术,将囊肿内所含的胰液引流至正常十二指肠。术后过程顺利。病例2,一名6个月大的男孩在无创伤的情况下出现突发性腹腔内出血。出血部位确定为回盲动脉,通过缝合实现了止血。由于动脉壁破裂的原因仍不明,对出血点附近的组织进行了活检。活检组织为肠黏膜。首次手术后患者反复出现腹痛,计算机断层扫描显示出血点附近有一个重复囊肿。因此,我们切除了肠重复畸形。病理结果显示肠重复畸形包含肠黏膜、异位胃黏膜和胰腺组织。术后过程顺利。

结论

无创伤性的腹腔内动脉出血是一种极为罕见的情况,且难以确定其病因。据我们所知,这是首例因肠重复畸形导致腹腔内动脉出血的报告。对于婴儿不明原因的腹腔内动脉出血病例,应怀疑出血点附近存在肠重复畸形。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd7/7085490/687f8ec92eb0/40792_2020_820_Fig1_HTML.jpg

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