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带状疱疹后出现短暂腹壁膨隆的假性疝:一例报告

Pseudohernia Following Herpes Zoster Presenting With Transient Abdominal Wall Bulging: A Case Report.

作者信息

Kei Nagatani, Takahiko Tsunoda

机构信息

Dermatology, Yamagata City Hospital Saiseikan, Yamagata, JPN.

出版信息

Cureus. 2025 Aug 26;17(8):e91076. doi: 10.7759/cureus.91076. eCollection 2025 Aug.

DOI:10.7759/cureus.91076
PMID:41018410
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12464513/
Abstract

Herpes zoster (HZ), caused by reactivation of latent varicella-zoster virus within the sensory ganglia, typically presents with painful vesicular eruptions. While motor nerve involvement is uncommon, it can occasionally lead to abdominal wall pseudohernia. Pseudohernia results from denervation and paralysis of abdominal muscles in the absence of a fascial defect, and is easily mistaken for a true hernia. We report the case of a 78-year-old man who developed a left-sided abdominal wall bulge shortly after the onset of HZ rash in the T10-T12 dermatomes. The bulge became prominent when standing but diminished in the supine position. CT revealed asymmetric thinning of the internal oblique and transversus abdominis muscles at the T11 level, with preservation of fascial continuity and no protrusion of intra-abdominal contents. These findings, combined with the close anatomical correspondence between the skin rash and the innervation of affected muscles, supported the diagnosis of HZ-related pseudohernia. Differential diagnoses such as diabetic truncal neuropathy, postsurgical changes, scarring myopathy, and localized fat atrophy were considered but excluded based on clinical history and imaging. The patient was managed conservatively with antiviral therapy and neuropathic pain control, leading to complete resolution of the bulge within three months. This case emphasizes that when abdominal wall bulging occurs near recent HZ skin lesions, pseudohernia should be strongly suspected. Recognition of this condition is essential to avoid misdiagnosis and unnecessary surgical procedures. Diagnosis can be supported by both clinical findings, including reduction of the bulge in the supine position, and imaging evidence of muscle thinning without a hernial defect. Prognosis is generally favorable, as most patients recover with conservative management alone.

摘要

带状疱疹(HZ)由感觉神经节内潜伏的水痘-带状疱疹病毒重新激活引起,通常表现为疼痛性水疱疹。虽然运动神经受累并不常见,但偶尔可导致腹壁假性疝。假性疝是在没有筋膜缺损的情况下,腹部肌肉失神经支配和麻痹所致,很容易被误诊为真性疝。我们报告一例78岁男性,在T10 - T12皮节出现HZ皮疹后不久,左侧腹壁出现隆起。站立时隆起明显,仰卧位时减轻。CT显示T11水平腹内斜肌和腹横肌不对称变薄,筋膜连续性保留,无腹腔内容物突出。这些发现,结合皮疹与受累肌肉神经支配之间密切的解剖对应关系,支持了HZ相关假性疝的诊断。考虑了诸如糖尿病性躯干神经病、术后改变、瘢痕性肌病和局限性脂肪萎缩等鉴别诊断,但根据临床病史和影像学检查予以排除。患者接受抗病毒治疗和神经性疼痛控制的保守治疗,三个月内隆起完全消退。该病例强调,当腹壁隆起发生在近期HZ皮肤病变附近时,应高度怀疑假性疝。认识到这种情况对于避免误诊和不必要的手术至关重要。仰卧位时隆起减轻等临床发现以及无疝缺损的肌肉变薄的影像学证据均可支持诊断。预后通常良好,因为大多数患者仅通过保守治疗即可康复。