Case Report: Misdiagnosed Primary Intramuscular Hydatid Cyst of the Deltoid Muscle in a Male Patient
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 1
- 试验地点
- 1
- 主要终点
- Complete recovery of shoulder function without recurrence
研究概览
简要总结
This case report describes a rare parasitic cyst called a hydatid cyst located in the shoulder muscle (deltoid) of a 29-year-old male. The patient initially presented with a painless, gradually enlarging swelling over the left shoulder. It was misdiagnosed as a synovial cyst and treated with corticosteroids, which caused local inflammation and purulent discharge. Blood tests for Echinococcus antibodies were negative. Ultrasound and MRI revealed a well-defined intramuscular cyst confined to the deltoid muscle. Surgical excision confirmed the diagnosis, and the patient received postoperative albendazole therapy for three months. Follow-up showed complete healing, restoration of shoulder function, and no recurrence. This case highlights the importance of considering hydatid disease in unusual muscle locations, particularly in endemic areas, to avoid misdiagnosis and ensure proper treatment.
详细描述
This report presents a rare case of a primary intramuscular hydatid cyst confined to the deltoid muscle in a 29-year-old male. The patient had a seven-month history of a gradually enlarging swelling in the left shoulder. Initially misdiagnosed as a synovial cyst, he received corticosteroid injection, which led to pain, erythema, and purulent discharge. Physical examination revealed a 10 cm fluctuant mass over the posterolateral deltoid. Serology for Echinococcus antibodies was negative. Ultrasound showed a well-defined, anechoic intramuscular cyst measuring 7 × 8 × 10 cm. MRI confirmed a fluid-filled cyst confined to the deltoid muscle, without involvement of bone, tendon, or joint structures. Under local anesthesia, the cyst was completely excised, and the cavity was irrigated with 10% povidone-iodine. Histopathology confirmed a non-fertile hydatid cyst (Echinococcus granulosus) without malignancy. Postoperative therapy included albendazole 400 mg daily for three months. Follow-up at six weeks showed complete wound healing, full shoulder function, and no recurrence. This case underscores the diagnostic challenges of intramuscular hydatid cysts, especially with negative serology, and highlights the importance of imaging, histopathology, and careful surgical management in endemic regions.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 120 Years(Adult, Older Adult)
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Male patient Age 18 years or older Diagnosed with primary intramuscular hydatid cyst of the deltoid muscle
排除标准
- •Patients with cysts in other organs (liver, lungs) Patients with systemic infection or immunocompromised status Patients who did not undergo surgical excision
结局指标
主要结局
Complete recovery of shoulder function without recurrence
时间窗: 6 weeks postoperatively
Monitoring for surgical site infection, serological status, and general patient well-being following treatment.
次要结局
未报告次要终点
研究者
Mohanad Nasani
Dr. Mohanad Nasani
Al-Shahba Specialized Hospital
