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孤立性肌肉囊尾蚴病两例报告:一种罕见的儿童假性肿瘤

Two Case Reports of Isolated Intramuscular Cysticercosis: An Uncommon Pediatric Pseudotumor.

作者信息

Gaur Shubhi, Parihar Pratap S, Nimodia Devyansh

机构信息

Department of Radiodiagnosis, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

出版信息

Cureus. 2024 Aug 30;16(8):e68206. doi: 10.7759/cureus.68206. eCollection 2024 Aug.

DOI:10.7759/cureus.68206
PMID:39347323
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11439477/
Abstract

, the pig tapeworm, produces larvae that cause cysticercosis, a common parasitic disease of the human nervous system including the brain. The disease is native to countries like Central and South America, Eastern Europe, Africa, India, and Indonesia. Cysticercosis is endemic in North India, particularly in Bihar, Uttar Pradesh, and Punjab. Asymptomatic cysts may have a history of trauma, while lower extremity involvement is less common. Isolated muscle involvement typically has no lethal consequences. Two cases, both pediatric, were diagnosed with intramuscular cysticercosis without involvement of the brain parenchyma. The patients received oral prednisolone therapy for seven days, followed by albendazole for 28 days. The swellings decreased in size and no new swellings or symptoms appeared during the two- and four-week follow-ups. At a three-month follow-up, the swellings completely resolved. Neurocysticercosis is a commonly encountered infection of the human central nervous system and one of the major causes of acquired epilepsy globally. Most cases are asymptomatic and go undiagnosed, with the first case likely due to trauma. Diagnosis is often delayed or overlooked due to vague clinical symptoms. Clinical differential diagnoses for intramuscular cysticercosis include lipomas, epidermoid cysts, neuromas, neurofibromas, pseudoganglia, sarcomas, myxomas, pyomyositis, cold abscess, and tuberculous lymphadenitis. High-resolution ultrasound is the most accurate method for diagnosing intramuscular cysticercosis, as it is quick, simple, and less expensive. Muscular cysticercosis sonographic patterns can be categorized into four types: first degree, uneven, irregular, and calcified. Magnetic resonance imaging (MRI) is the most accurate way to diagnose intramuscular cysticercosis, as it can show live scolex, cysts, and degenerating cysts. In every case, there is edema to varied degrees, with fluid-filled lesions without peripheral enhancement visible in early stages and peripheral rim augmentation and perilesional edema observed in later stages.

摘要

猪带绦虫会产生幼虫,导致囊尾蚴病,这是一种常见的人类神经系统寄生虫病,包括脑部感染。该病原产于中美洲、南美洲、东欧、非洲、印度和印度尼西亚等国家。囊尾蚴病在印度北部流行,尤其是在比哈尔邦、北方邦和旁遮普邦。无症状囊肿可能有外伤史,而下肢受累较少见。孤立的肌肉受累通常没有致命后果。有两例儿科患者被诊断为肌肉囊尾蚴病,未累及脑实质。患者接受了为期七天的口服泼尼松龙治疗,随后服用阿苯达唑28天。肿胀大小减小,在两周和四周的随访中未出现新的肿胀或症状。在三个月的随访中,肿胀完全消退。神经囊尾蚴病是人类中枢神经系统常见的感染,也是全球获得性癫痫的主要原因之一。大多数病例无症状且未被诊断,首例病例可能与外伤有关。由于临床症状模糊,诊断往往延迟或被忽视。肌肉囊尾蚴病的临床鉴别诊断包括脂肪瘤、表皮样囊肿、神经瘤、神经纤维瘤、假神经节、肉瘤、黏液瘤、脓性肌炎、寒性脓肿和结核性淋巴结炎。高分辨率超声是诊断肌肉囊尾蚴病最准确的方法,因为它快速、简单且成本较低。肌肉囊尾蚴病的超声图像模式可分为四种类型:一度、不均匀、不规则和钙化。磁共振成像(MRI)是诊断肌肉囊尾蚴病最准确的方法,因为它可以显示活的头节、囊肿和退化的囊肿。在每种情况下,都有不同程度的水肿,早期可见无周边强化的液性病变,后期可见周边边缘强化和病灶周围水肿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b774/11439477/17986f3735f0/cureus-0016-00000068206-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b774/11439477/9f126b3ee025/cureus-0016-00000068206-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b774/11439477/d1a3051be14e/cureus-0016-00000068206-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b774/11439477/3e52769ed4bd/cureus-0016-00000068206-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b774/11439477/17986f3735f0/cureus-0016-00000068206-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b774/11439477/9f126b3ee025/cureus-0016-00000068206-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b774/11439477/d1a3051be14e/cureus-0016-00000068206-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b774/11439477/3e52769ed4bd/cureus-0016-00000068206-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b774/11439477/17986f3735f0/cureus-0016-00000068206-i04.jpg

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本文引用的文献

1
Isolated intramuscular cysticercosis: Clinicopathological features, diagnosis and management - A review.孤立性肌肉囊尾蚴病:临床病理特征、诊断与治疗——综述
J Clin Orthop Trauma. 2016 Oct-Dec;7(Suppl 2):243-249. doi: 10.1016/j.jcot.2016.06.016. Epub 2016 Jun 30.
2
Solitary intramuscular cysticercosis-A report of two cases.孤立性肌肉囊尾蚴病——两例报告
Australas Med J. 2011;4(1):58-60. doi: 10.4066/AMJ.2011.483. Epub 2011 Jan 31.
3
Role of ultrasonography and magnetic resonance imaging in the diagnosis of intramuscular cysticercosis.
超声和磁共振成像在肌肉囊尾蚴病诊断中的作用。
Skeletal Radiol. 2012 Sep;41(9):1061-6. doi: 10.1007/s00256-011-1320-2. Epub 2011 Nov 19.
4
Subcutaneous and intramuscular cysticercosis: high-resolution sonography.皮下及肌肉囊尾蚴病:高分辨率超声检查
Indian J Dermatol Venereol Leprol. 2009 Sep-Oct;75(5):515-6. doi: 10.4103/0378-6323.55404.
5
A 37-year-old man with a painless growing mass of the thorax.一名37岁男性,胸部有一个无痛性生长的肿块。
Clin Orthop Relat Res. 2010 Apr;468(4):1193-8. doi: 10.1007/s11999-009-1057-6. Epub 2009 Aug 28.
6
Human cysticercosis and Indian scenario: a review.人类囊尾蚴病与印度情况:综述
J Biosci. 2008 Nov;33(4):571-82. doi: 10.1007/s12038-008-0075-y.
7
Masseter cysticercosis - a rare case diagnosed on ultrasound.
Dentomaxillofac Radiol. 2008 Feb;37(2):113-6. doi: 10.1259/dmfr/31885135.
8
Cysticercosis: an emerging parasitic disease.囊尾蚴病:一种新出现的寄生虫病。
Am Fam Physician. 2007 Jul 1;76(1):91-6.
9
MRI and ultrasound in solitary muscular and soft tissue cysticercosis.孤立性肌肉和软组织囊尾蚴病的磁共振成像与超声检查
Skeletal Radiol. 2005 Nov;34(11):722-6. doi: 10.1007/s00256-005-0954-3. Epub 2005 Sep 16.
10
Sonographic appearances in cysticercosis.囊尾蚴病的超声表现。
J Ultrasound Med. 2004 Mar;23(3):423-7. doi: 10.7863/jum.2004.23.3.423.