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本文引用的文献

1
Isolated Intramuscular Cysticercosis in Children: A Case Report.儿童孤立性肌囊虫病:病例报告。
Turkiye Parazitol Derg. 2022 Mar 1;46(1):72-74. doi: 10.4274/tpd.galenos.2020.6613.
2
Taenia solium taeniasis/cysticercosis: From parasite biology and immunology to diagnosis and control.猪带绦虫病/囊尾蚴病:从寄生虫生物学和免疫学角度探讨诊断和防治。
Adv Parasitol. 2021;112:133-217. doi: 10.1016/bs.apar.2021.03.003. Epub 2021 Apr 8.
3
Cytological diagnosis of cysticercosis: Role of FNAC with On-Site evaluation.囊尾蚴病的细胞学诊断:现场评估的细针穿刺抽吸活检(FNAC)的作用
IDCases. 2018 Dec 11;15:e00477. doi: 10.1016/j.idcr.2018.e00477. eCollection 2019.
4
Prevalence and risk factors for Taenia solium taeniasis in Kaniyambadi block, Tamil Nadu, South India.印度南部泰米尔纳德邦卡尼亚姆巴迪区猪带绦虫病的患病率及危险因素
Indian J Public Health. 2014 Jul-Sep;58(3):202-3. doi: 10.4103/0019-557X.138638.
5
Intramuscular cysticercosis--the solitary reaper.肌肉囊尾蚴病——孤独的收割者。
Ann Afr Med. 2014 Jan-Mar;13(1):53-4. doi: 10.4103/1596-3519.126955.
6
Intramuscular cysticercosis: starry sky appearance.肌内囊尾蚴病:星空样表现。
QJM. 2014 Jun;107(6):459-61. doi: 10.1093/qjmed/hct243. Epub 2013 Dec 3.
7
A rare case of disseminated cysticercosis.一例罕见的播散性囊尾蚴病。
Trop Parasitol. 2012 Jul;2(2):138-41. doi: 10.4103/2229-5070.105183.
8
Diagnostic criteria for neurocysticercosis, revisited.神经囊尾蚴病的诊断标准,再探讨。
Pathog Glob Health. 2012 Sep;106(5):299-304. doi: 10.1179/2047773212Y.0000000025.
9
Intramuscular cysticercosis diagnosed on ultrasonography in thigh: A rare case report.超声诊断大腿部肌肉囊尾蚴病:一例罕见病例报告。
N Am J Med Sci. 2010 Mar;2(3):162-4.
10
Cytomorphological spectrum of subcutaneous and intramuscular cysticercosis: A study of 22 cases.皮下及肌肉囊尾蚴病的细胞形态学谱:22例研究
J Cytol. 2010 Oct;27(4):123-6. doi: 10.4103/0970-9371.73294.

一名年轻女性孤立性肱桡肌症状性囊尾蚴病:一种经手术治疗的罕见病例。

Isolated brachioradialis symptomatic cysticercosis in a young female: A rare entity surgically managed.

作者信息

Dogra Shavinder, Misra Pratibha, Bedi Tejpal Singh, Jacob Mathews

机构信息

Head of Department (Surgery), 151 Base Hospital, C/o 99 APO, India.

Senior Advisor (Pathology & Biochemistry), 151 Base Hospital, C/o 99 APO, India.

出版信息

Med J Armed Forces India. 2024 Dec;80(Suppl 1):S288-S291. doi: 10.1016/j.mjafi.2023.04.005. Epub 2023 Jun 4.

DOI:10.1016/j.mjafi.2023.04.005
PMID:39734879
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11670622/
Abstract

Taenia solium is a parasite and is endemic in the developing countries due to various unhygienic faecal practices. The disseminated form is commoner with the brain being the most common site of affliction. This report is of a young female patient with complaints of an insidious and progressive swelling of the right forearm. Clinicoradiological features were suggestive of an isolated myocysticercosis which was symptomatic with restricted pronation and supination. The symptoms persisted post a course of Albendazole, and the cyst had to be excised as it was impinging on the median and radial nerves. The patient has been asymptomatic after a 3-month post-operative period with no signs or imaging evidence of residual disease. The presence of isolated intramuscular cysticercosis is an extremely rare and a high index of suspicion is needed for early diagnosis. Although medical management is extremely effective, surgical excision may be required in certain cases.

摘要

猪带绦虫是一种寄生虫,由于各种不卫生的粪便处理方式,在发展中国家呈地方性流行。播散型较为常见,其中脑部是最常见的受累部位。本报告介绍了一名年轻女性患者,她主诉右前臂出现隐匿性、进行性肿胀。临床放射学特征提示为孤立性肌肉囊尾蚴病,伴有旋前和旋后受限的症状。在接受阿苯达唑治疗后症状仍持续存在,由于囊肿压迫正中神经和桡神经,不得不将其切除。术后3个月患者一直无症状,没有残留疾病的体征或影像学证据。孤立性肌肉囊尾蚴病极为罕见,早期诊断需要高度怀疑。虽然药物治疗非常有效,但在某些情况下可能需要手术切除。