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从解剖学和组织学角度看多发性空肠憩室病:一例报告

Multiple jejunal diverticulosis, from an anatomical and histological view: A case report.

作者信息

Schmidt Patricia, Perniss Alexander, Nassenstein Christina, Keller Hanno, Deckmann Klaus

机构信息

Institute for Anatomy and Cell Biology, Justus-Liebig-University Giessen, Giessen 35392, Hesse, Germany.

Leibniz Institute on Aging, Fritz Lipmann Institute, Jena 07745, Thuringia, Germany.

出版信息

World J Gastrointest Surg. 2025 Jul 27;17(7):104985. doi: 10.4240/wjgs.v17.i7.104985.

Abstract

BACKGROUND

Here, we report a case of jejunal diverticulosis from an anatomical and histological view. During the "Gross Anatomy course," we found multiple jejunal diverticula along a total length of 208 cm of intestine.

CASE SUMMARY

After opening the intestinal tract, we counted 232 jejunal diverticulum entry points with a diameter of up to 2 cm and observed connections between the diverticula that created shortcuts between two distinct intestinal parts. Interestingly, we observed an extreme longitudinal striation on the intestinal parts hosting diverticula. Thorough vessel preparation utilizing a dissecting microscope confirmed that all investigated arteriae rectae ended in a diverticulum. Histological and immunohistochemical investigations revealed that intestinal villi of diverticula were smaller and less prominent than control tissue and that the stratum longitudinale, as well as the stratum circular, were much thinner in the diverticula compared to control tissue. Neither submucosal nor mesenteric plexus could be detected in the diverticula. However, vasoactive intestinal peptide-positive nerve fibers and villin-positive brush border could only be detected in control tissue. This indicates that jejunal diverticulosis is associated with abnormalities of the smooth muscles and a disorder of innervation.

CONCLUSION

Jejunal diverticulosis originates from mesenteric vessels, featuring smooth muscle changes, absent innervation, and thinning of tissue layers.

摘要

背景

在此,我们从解剖学和组织学角度报告一例空肠憩室病病例。在“大体解剖学课程”期间,我们在一段总长208厘米的肠管上发现了多个空肠憩室。

病例摘要

打开肠道后,我们清点了232个直径达2厘米的空肠憩室入口点,并观察到憩室之间的连接,这些连接在两个不同肠段之间形成了捷径。有趣的是,我们在有憩室的肠段观察到了极端的纵向条纹。利用解剖显微镜进行彻底的血管准备证实,所有研究的直动脉均终止于一个憩室。组织学和免疫组织化学研究显示,憩室的肠绒毛比对照组织小且不明显,与对照组织相比,憩室的纵肌层和环肌层都薄得多。在憩室中未检测到黏膜下神经丛和肠系膜神经丛。然而,仅在对照组织中检测到血管活性肠肽阳性神经纤维和绒毛蛋白阳性刷状缘。这表明空肠憩室病与平滑肌异常和神经支配紊乱有关。

结论

空肠憩室病起源于肠系膜血管,其特征为平滑肌改变、无神经支配和组织层变薄。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf4f/12305284/c3f3beb524bc/wjgs-17-7-104985-g001.jpg

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