Suppr超能文献

3例播散性肺泡型棘球蚴病复发性多器官受累:病例报告

Recurrent multiple-organ involvement of disseminated alveolar echinococcosis in 3 patients: Case report.

作者信息

Xu Leilei, Siyiti Sikandaer, Song Xinghua, Wen Hao, Ding Liwen, Yunus Akbar, Tian Zheng, Wang Chong, Chen Jiangtao

机构信息

Orthopedic Department, The First Affiliated Hospital of Xinjiang Medical University Orthopedic Department, The Sixth Affiliated Hospital of Xinjiang Medical University Xinjiang Medical University, Urumqi, PR China.

出版信息

Medicine (Baltimore). 2017 Oct;96(42):e7632. doi: 10.1097/MD.0000000000007632.

Abstract

RATIONALE

Alveolar echinococcosis (AE) is a rare but highly malignant form of echinococcosis caused by Echinococcus multilocularis. There have been very few reports on multiple-organ AE, especially AE in bones. Here we report 3 rare cases of disseminated multiple-organ AE from western China and its neighboring areas.

PATIENT CONCERNS

Patient 1 had back and left hip pain, headache, and weakness in left lower limb, often with minor epilepsy and fluctuation of blood pressure. Lower limbs Babinski sign was positive and muscular tension was above normal range. The second patient had pain in lower limbs and chest discomfort without fever, cough, sputum, chest tightness, or hemoptysis. Patient 3 had masses and pain in the back side of his right shoulder.

DIAGNOSES

The patients had been treated for AE multiple times and were positive for serum hydatid antigens. They were diagnosed as multiorgan AE involving liver, spinal cord, and many other organs.

INTERVENTIONS

The patients had undergone surgeries to decompress the spinal cord, remove lesions from tissues as required, and were put on albendazole for at least 2 years.

OUTCOMES

The patients responded well and AE recurrence has not occurred.

LESSONS

All 3 cases experienced multiple recurrences of AE due to missed diagnosis, misdiagnosis, or inappropriate treatment, which resulted in metastatic multiorgan AE. These cases demonstrated the need for more policy attention to battle AE endemic in western China.

摘要

原理

泡型包虫病(AE)是由多房棘球绦虫引起的一种罕见但高度恶性的包虫病形式。关于多器官AE的报道非常少,尤其是骨骼中的AE。在此,我们报告3例来自中国西部及其周边地区的罕见播散性多器官AE病例。

患者情况

患者1有背部和左髋部疼痛、头痛以及左下肢无力,常伴有轻度癫痫和血压波动。下肢巴宾斯基征阳性,肌张力高于正常范围。第二名患者有下肢疼痛和胸部不适,无发热、咳嗽、咳痰、胸闷或咯血。患者3右肩后侧有肿块和疼痛。

诊断

这些患者曾多次接受AE治疗,血清包虫抗原呈阳性。他们被诊断为累及肝脏、脊髓和许多其他器官的多器官AE。

干预措施

患者接受了脊髓减压手术,根据需要切除组织中的病变,并服用阿苯达唑至少2年。

结果

患者反应良好,未发生AE复发。

经验教训

所有3例病例均因漏诊、误诊或治疗不当而经历了AE多次复发,导致转移性多器官AE。这些病例表明需要更多政策关注以应对中国西部的AE流行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e9f/5662347/31f93be1bca2/medi-96-e7632-g002.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验