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肠浆膜下额外肌层:一种特殊的肠道结构。

Subserosal Supernumerary Muscle Layer of the Intestine: A Peculiar Bowel.

作者信息

Gupta Mehul, Kumar Arun, Singla Vitish, Aggarwal Sandeep, Das Prasenjit

机构信息

Department of Surgery, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.

Department of Pathology, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.

出版信息

Cureus. 2024 May 11;16(5):e60096. doi: 10.7759/cureus.60096. eCollection 2024 May.

Abstract

The presence of a supernumerary subserosal muscle layer of the bowel is an extremely unusual congenital development. The following is a report of diffuse involvement of the intestine with a supernumerary subserosal muscle coat. The current patient, a 29-year-old male, was evaluated in January 2022 for a long-standing history of subacute intestinal obstruction (SAIO). A preoperative CT scan of the abdomen and pelvis suggested mild dilatation and clumping of ileal loops in the right iliac fossa, with a subtle wall thickening of up to 5 mm. Intraoperatively, dense adhesions were noted between clumped bowel loops and the anterior abdominal wall. Following adhesiolysis, ileocecal resection with ileocolic anastomosis was done. The histopathological examination of the resected bowel segment showed irregular hypertrophy of circular and longitudinal muscle layers with the presence of an additional smooth muscle coat outer to the outer longitudinal layer that was seen in the ileum as well as the appendix. No evidence of vacuolar degeneration was noted, and ganglion cells were seen to be adequately present. The presence of additional smooth muscle bundles in the subserosa was confirmed with positive actin immunostaining. Additionally, CD117 staining was done that revealed a normal network of interstitial cells of Cajal. No evidence of active inflammation was noted in the resected bowel segment. Findings from the current case bring to light an extremely rare malformation of the muscularis propria of the intestine, namely a supernumerary subserosal muscle coat.

摘要

肠道浆膜下额外肌层的存在是一种极其罕见的先天性发育异常。以下是一篇关于肠道弥漫性受累并伴有浆膜下额外肌层的报告。本例患者为一名29岁男性,于2022年1月因长期亚急性肠梗阻(SAIO)病史接受评估。术前腹部和盆腔CT扫描显示右髂窝回肠袢轻度扩张和聚集,肠壁轻度增厚达5mm。术中发现聚集的肠袢与前腹壁之间有致密粘连。粘连松解后,行回盲部切除并回结肠吻合术。切除肠段的组织病理学检查显示环形和纵行肌层不规则肥厚,在回肠和阑尾的外纵行肌层外侧可见一层额外的平滑肌层。未发现空泡变性证据,可见神经节细胞数量充足。肌动蛋白免疫染色阳性证实浆膜下存在额外的平滑肌束。此外,进行了CD117染色,显示 Cajal间质细胞网络正常。切除的肠段未发现活动性炎症迹象。本例的发现揭示了一种极其罕见的肠道固有肌层畸形,即浆膜下额外肌层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9520/11164246/19eda89e4bb9/cureus-0016-00000060096-i01.jpg

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