坐骨臀肌钙化性滑囊炎：一例报告
Calcifying Bursitis ischioglutealis: A Case report.
作者信息
Schuh Alexander, Narayan Chirag Thonse, Schuh Ralph, Hönle Wolfgang
机构信息
Research Unit Orthopedics and General Surgery, Neumarkt Clinic, 92318 Neumarkt, Germany; Orth.Med Weiden, 92637 Weiden, Germany.
Indian Orthopaedic Research Group.
出版信息
J Orthop Case Rep. 2011 Oct-Dec;1(1):16-8.
INTRODUCTION
The ischiogluteal bursa is an inconstant anatomical finding located between the ischial tuberosity and the gluteus maximus. Ischiogluteal bursitis is a rare disorder.
CASE REPORT
We report the case of a 43-year-old female patient with bilateral calcifying ischiogluteal bursitis. The patient had no relevant medical history of systemic illness or major trauma to the buttock. After aspiration of both ischiogluteal bursitis which delievered calcareous deposits and instillation of a mixture of 1cc betamethasone (6 mg) and 4 cc of 1% lidocaine the patient was out of any complaints.
CONCLUSION
Calcifying ischiogluteal bursitis is a rare entity but easily diagnosed on radiographs. Aspiration and local steroid instillation give good relief from symptoms.
引言
坐骨臀肌滑囊是位于坐骨结节和臀大肌之间的一种不恒定的解剖结构。坐骨臀肌滑囊炎是一种罕见的疾病。
病例报告
我们报告一例43岁双侧钙化性坐骨臀肌滑囊炎女性患者。该患者无全身性疾病或臀部重大创伤的相关病史。在抽吸双侧坐骨臀肌滑囊并排出钙质沉积物后，注入1毫升倍他米松（6毫克）和4毫升1%利多卡因的混合液，患者症状消失。
结论
钙化性坐骨臀肌滑囊炎是一种罕见的病症，但在X线片上易于诊断。抽吸和局部注射类固醇可有效缓解症状。
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