Abstract
小兒顱骨板障處血腫是一種罕見的疾病，到目前為止文獻上只報告九個案例。我們報導一位三歲大的女童，她的臨床表徵是右側頭頂部的頭皮持續性腫大。經影像學檢查顯示在變寬的頭頂部顱骨板障處有一骨質溶解合併中央囊腫形成的病癥。開刀清除血腫時發現，此損害板障的內側顱骨面完整，所以被完整保留下來。壹個月後的追蹤顯示出此缺損處已完全重新形成骨質，無任何顱骨缺損。
Diploic hematoma is an uncommon lesion of the skull and only nine cases have been reported. We report a 3-year-old girl who presented a progressive swelling of her right parietal scalp. Image studies revealed an osteolytic lesion in the widened parietal diploic bone with a central cyst formation. Operation was performed and diploic hematoma was found. It was evacuated with preservation of the inner cortical bone. One month after surgery, the skull bone showed excellent remodeling, and no bony defect. A relationship between the anticoagulants and the diploic hematoma is suggested. Consideration of treatment for diploic hematoma depends on the integrity of the inner table.
Diploic hematoma is an uncommon lesion of the skull and only nine cases have been reported. We report a 3-year-old girl who presented a progressive swelling of her right parietal scalp. Image studies revealed an osteolytic lesion in the widened parietal diploic bone with a central cyst formation. Operation was performed and diploic hematoma was found. It was evacuated with preservation of the inner cortical bone. One month after surgery, the skull bone showed excellent remodeling, and no bony defect. A relationship between the anticoagulants and the diploic hematoma is suggested. Consideration of treatment for diploic hematoma depends on the integrity of the inner table.
| Original language | American English |
|---|---|
| Pages (from-to) | 177-180 |
| Journal | Formosan Journal of Surgery |
| Volume | 40 |
| Issue number | 4 |
| State | Published - 2007 |