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肉芽肿性多血管炎合并肠囊样积气 1 例报告。

Pneumatosis cystoides intestinalis in granulomatosis with polyangiitis: a case report.

机构信息

Department of Rheumatology and Immunology, Beijing Friendship Hospital, Capital Medical University, 95 Yong'an Road, Beijing, 100050, China.

Department of Radiology, Beijing Friendship Hospital, Capital Medical University, 95 Yong'an Road, Beijing, 100050, China.

出版信息

Clin Rheumatol. 2024 Dec;43(12):3809-3814. doi: 10.1007/s10067-024-07153-6. Epub 2024 Oct 2.

Abstract

This study aims to investigate the clinical manifestations, imaging features, and treatment considerations in the rare occurrence of pneumatosis cystoides intestinalis (PCI) within the context of granulomatosis with polyangiitis (GPA). We present the case of a 71-year-old Chinese woman diagnosed with GPA, who, despite exhibiting fatigue, knee pain, and nasosinusitis, remained asymptomatic for PCI. Regular follow-up revealed laboratory and imaging evidence indicative of clinical relapse. The patient received GPA treatment but was not specifically managed for PCI. Serial abdominal CT scans were performed to monitor the progression of PCI. Radiological diagnosis confirmed the presence of gas within the colon wall, indicating pneumatosis cystoides intestinalis. Notably, the patient remained asymptomatic for abdominal complaints. Despite ongoing GPA treatment, a follow-up CT scan 2 months later revealed persistent gas within the colon wall, suggesting a persistent state of PCI. Patient consent was obtained for the publication of this case report, and ethical approval was not obtained as this study constitutes a retrospective review. This case underscores the importance of recognizing pneumatosis cystoides intestinalis as a potential complication in GPA patients, even in the absence of typical abdominal symptoms. Further research is warranted to elucidate the underlying mechanisms and optimal management strategies for this rare association. Key points • Rare association: This case report sheds light on the uncommon occurrence of pneumatosis cystoides intestinalis (PCI) within the context of granulomatosis with polyangiitis (GPA), adding to the understanding of the spectrum of manifestations of GPA. • Clinical manifestations: Despite being diagnosed with GPA and experiencing symptoms such as fatigue, knee pain, and nasosinusitis, the patient remained asymptomatic for PCI, emphasizing the importance of vigilant clinical monitoring in GPA patients. • Imaging features: Radiological imaging, including serial abdominal CT scans, played a crucial role in diagnosing and monitoring the progression of PCI in the absence of typical abdominal complaints, highlighting the utility of imaging modalities in detecting silent manifestations of gastrointestinal complications in GPA. • Treatment considerations: The case highlights the challenge of managing PCI in GPA patients, especially when asymptomatic, and raises questions about the optimal management strategies for such rare associations, underscoring the need for further research in this area.

摘要

本研究旨在探讨罕见的皮肌炎合并多血管炎(GPA)患者并发肠囊样积气(PCI)的临床表现、影像学特征和治疗注意事项。我们报告了一例 71 岁的中国女性 GPA 患者,尽管她表现出疲劳、膝关节疼痛和鼻旁窦炎,但没有 PCI 的症状。定期随访显示出实验室和影像学证据表明临床复发。患者接受了 GPA 治疗,但没有专门针对 PCI 进行管理。连续进行腹部 CT 扫描以监测 PCI 的进展。放射学诊断证实结肠壁内存在气体,提示肠囊样积气。值得注意的是,患者没有出现腹部症状。尽管 GPA 治疗仍在继续,但 2 个月后的后续 CT 扫描显示结肠壁内仍有气体,表明 PCI 持续存在。本病例报告获得了患者的同意,并获得了伦理批准,因为本研究属于回顾性研究。本病例强调了认识到 PCI 是 GPA 患者的一种潜在并发症的重要性,即使没有典型的腹部症状。需要进一步研究以阐明这种罕见关联的潜在机制和最佳管理策略。 关键点 • 罕见关联:本病例报告揭示了皮肌炎合并多血管炎(GPA)患者中肠囊样积气(PCI)的罕见发生,增加了对 GPA 表现谱的认识。 • 临床表现:尽管诊断为 GPA 并出现疲劳、膝关节疼痛和鼻旁窦炎等症状,但患者没有 PCI 的症状,强调了在 GPA 患者中进行警惕性临床监测的重要性。 • 影像学特征:影像学,包括连续腹部 CT 扫描,在没有典型腹部症状的情况下对诊断和监测 PCI 的进展发挥了关键作用,强调了影像学在检测 GPA 患者胃肠道并发症隐匿表现方面的作用。 • 治疗注意事项:该病例强调了在 GPA 患者中管理 PCI 的挑战,尤其是在无症状的情况下,并提出了关于此类罕见关联的最佳管理策略的问题,突出了在这一领域进一步研究的必要性。

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