Retroperitoneal hydatid cyst

  • 文章类型: Case Reports
    包虫病可以影响人体任何器官。腰大肌包虫囊肿的发生是罕见的,仅占病例的1-3%,甚至在流行地区。然而,多发性囊肿的存在更为罕见。
    方法:一名来自农村地区的40岁女性出现腹痛。体格检查显示右侧软骨病有压痛。七年前她有肺包虫膀胱切除术史。放射学检查显示,左腰大肌内有两个包虫囊肿。对两个包虫囊肿进行了膀胱切除术。患者服用阿苯达唑的剂量为15mg/kg,在最近一个月的随访预约中,患者未出现任何复发.
    此例表现为腰肌多发性包虫囊肿的罕见情况,强调在流行地区考虑非典型表现的重要性。
    结论:该病例突出了一名农村中年妇女腰大肌包虫囊肿的罕见性。早期识别,准确的放射学评估,适当的手术治疗对于积极的结果和避免感染等并发症至关重要,压缩附近的结构,或者过敏反应.
    UNASSIGNED: Hydatid disease can affect any human organ. The occurrence of hydatid cysts in psoas muscle is rare, accounting for only 1-3 % of cases, and even in endemic regions. However, the presence of multiple cysts is even more rare.
    METHODS: A 40-year-old female from a rural area presented with abdominal pain. Physical examination revealed tenderness in the right hypochondrium. Her medical history pulmonary hydatid cystectomy seven years ago. Radiology investigation showed a two-hydatid cyst within the left psoas major muscle. Cystectomy of two hydatid cyst was performed. The patient was prescribed albendazole at a dose of 15 mg/kg, and at the latest month\'s follow-up appointment, the patient did not experience any relapse.
    UNASSIGNED: This case presents a rare instance of multiple hydatid cysts in the psoas muscle, highlighting the importance of considering atypical presentations in endemic regions.
    CONCLUSIONS: This case highlights the rarity of psoas major muscle hydatid cysts in a middle-aged woman from a rural area. Early recognition, accurate radiological assessment, and proper surgical treatment are crucial for positive outcomes and averting complications like infection, compression of nearby structures, or anaphylactic reactions.
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  • 文章类型: Case Reports
    棘球蚴病是由细粒棘球蚴幼虫期产生的一种寄生虫病。骨包虫病在人类中很少见,仅在1-2%的包虫病病例中有报道。我们介绍了一名患者,该患者发展为左骨盆和股骨的包虫病,同侧髋关节软骨破坏,揭示了包虫囊肿的腹膜后位置。包虫骨必须存在于慢性单关节炎的鉴别诊断中。骨骼受累通常继发于我们必须研究的内脏包虫病。早期诊断可以根除和挽救骨骼和髋关节。延迟诊断总是充满复发和败血症的风险。
    Echinococcosis is a parasitic disease produced by the larval stage of Echinococcus granulosus. Hydatid disease of bone is rarely seen in humans and it has been reported in only 1-2% of cases of echinococcosis. We present a patient who developed hydatid disease of the left pelvic and femoral bones with cartilage destruction of the ipsilateral hip joint revealing a retroperitoneal location of hydatid cyst. Hydatid bone must be present in the differential diagnosis of chronic monoarthritis. Skeletal involvement is usually secondary to visceral hydatidosis that we must research. Early diagnosis allows eradication and salvage of the bone and the hip joint. Delayed diagnosis is always fraught with the risk of recurrence and sepsis.
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