摘要
從1980年1月到1986年10月，共收集23個已由病理證明為組織細胞症X的病例。其年齡範圍從3個月大到53歲。男女比例為13:10。此病之預後最差為發生於幼童期，其表現為急性散播型。若病人只有單一骨頭的病灶，其預後最好。此病常見有多處骨骼同時發生骨質溶解之病變。在這份報告裡，頭骨病灶最常見，次之為脊椎骨，而再後者為股骨，盆骨，肱骨及橈骨。
關鍵字
無資料並列摘要
From Jan. 1980 to Oct. 1986, 23 cases of histiocytosis X, proven by pathology, were reviewed. The age range was from 3 months to .53 years. The sex ratio of male to female was 13:10. Tge prognosis presented worse in the young childhood because of disseminated pattern from the onset. Satisfactory response to therapy was gained in the patient with solitary bone lesion but poor result in the case of disseminated form. Histiocytosis X always had multiple bone lesions with osteolytic character. In our series, skull bone was the most frequent site of bone involvement, whereas the other frequent site of bone involvement, whereas the other frequent site from more to less were spine, femur, pelvic, humerus and radius.
延伸閱讀
- Huang, Y. L., Jin, Y. T., Yan, Y. H., Lin, C. C., & Lin, L. M. (1987). 口腔X型組織細胞增多症之超微構造組織病理學及免疫組織生化學的探討. The Kaohsiung Journal of Medical Sciences, 3(3), 155-165. https://doi.org/10.6452/KJMS.198703.0155
- 林茂杉、秦德萍、李三剛、李超群、何善平（1988）。惡性纖維組織細胞瘤。中華放射線醫學雜誌，13(3)，279-284。https://www.airitilibrary.com/Article/Detail?DocID=10188940-198809-13-3-279-284-a
- 黃聖懿、田蕙芬（2009）。漿細胞骨髓瘤。當代醫學，(426)，287-299。https://doi.org/10.29941/MT.200904.0010
- 廖雅玲、盧金坊（1987）。結膜性的組織球細胞增多症X。中華民國眼科醫學會雜誌，26(1)，343-347。https://doi.org/10.30048/ACTASOS.198705.0061
- 蔡文雄、林凱信、林東燦、林國信、謝宏忠（1988）。組織球增多症－X併有廣泛性淋巴結病變－兩病例報告。Acta Paediatrica Sinica，29(2)，131-136。https://www.airitilibrary.com/Article/Detail?DocID=00016578-198804-29-2-131-136-a