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Isolated Forearm Swelling - A Rare Presentation of Soft Tissue Cysticercosis

机译:孤立的前臂肿胀-软组织囊性囊肿的罕见表现

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Cysticercosis is a common human infestation in the developing world. Neurocysticercosis is the most common clinical presentation of cysticercal infestation in the human body, but it may be rarely encountered in other body parts like skeletal muscle, subcutaneous tissue and eye. We report this case of an uncommon clinical presentation of soft tissue cysticercosis as an isolated forearm swelling. Only a few cases of cysticercosis presenting as isolated swelling in any body part have been reported in literature. A 30 year old lady presented with a painless swelling in the left forearm for about one year. It was diagnosed as cysticercosis located in the intermuscular plane between the brachioradialis and pronator teres and above the supinator muscles. Magnetic resonance imaging (MRI) and ultrasonography (USG) of the forearm confirmed a cystic lesion and revealed a scolex. She was treated with albendazole and steroids for three weeks but did not respond to medical treatment. The swelling was surgically excised. Hisptopathological examination of the cyst confirmed cysticercosis. Soft tissue cysticercosis presenting as an isolated forearm swelling is a rare presentation of cysticercosis. Treating physicians and surgeons need to have a high index of clinical suspicion for cysticercosis, especially in endemic areas in the developing nations, to facilitate an early diagnosis. Through this case report we also highlight that cysticercosis can be easily diagnosed by non invasive investigations like MRI and USG. It is usually medically treatable but may occasionally require surgical intervention as was needed in our case. This document gives formatting instructions for authors preparing papers for publication in the journal. Authors are encouraged to prepare manuscripts directly using this template. This template demonstrates format requirements for the Journal.
机译:囊尾osis病是发展中国家常见的人类感染。神经囊尾osis病是人体中最常见的囊性脑病临床表现,但在其他身体部位(如骨骼肌,皮下组织和眼睛)可能很少见到。我们报告这种情况的软组织囊尾osis病的罕见临床表现为孤立的前臂肿胀。在文献中仅报道了少数几例囊尾as病在任何身体部位均表现为孤立性肿胀。一名30岁的女士左前臂无痛肿胀约一年。它被诊断为囊尾osis虫病,位于radi臂和前旋肌之间的肌间平面内,在旋后肌上方。前臂的磁共振成像(MRI)和超声检查(USG)证实了一个囊性病变并显示了下丘。她接受了阿苯达唑和类固醇的治疗,持续了三周,但对药物的治疗没有反应。通过手术切除肿胀。囊肿的组织病理学检查证实为囊虫病。表现为孤立的前臂肿胀的软组织囊尾osis病是一种罕见的囊尾rc病表现。治疗医生和外科医生需要对囊尾rc病有高度的临床怀疑,特别是在发展中国家的流行地区,以促进早期诊断。通过该病例报告,我们还强调可以通过非侵入性检查(如MRI和USG)轻松诊断出囊尾rc病。它通常是可以治疗的,但有时可能需要根据我们的情况进行手术干预。本文档为作者准备要在期刊中发表的论文提供了格式说明。鼓励作者使用此模板直接准备手稿。该模板演示了日记的格式要求。

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