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來源資料
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題名 | Cytophagic Histiocytic Panniculitis--A Case Report and Review of the Literature=細胞吞噬性組織細胞性脂層炎--病例報告以及文獻回顧 |
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作者 | 林起翎; 陳國熏; Lin, Chi-ling; Chen, Gwo-shing; |
期刊 | 中華皮膚科醫學雜誌 |
出版日期 | 20070300 |
卷期 | 25:1 2007.03[民96.03] |
頁次 | 頁53-58 |
分類號 | 415.65 |
語文 | eng |
關鍵詞 | 細胞吞噬性組織細胞性脂層炎; Cytophagic histiocytic panniculitis; Histiocytic cytophagic panniculitis; Weber-Christian syndrome; |
中文摘要 | 一位四歲男童病患有發燒、腹痛以及數個青紅色皮下結節於下背及四肢,以小腿居多出現約有十天。實驗數據顯示白血球升高、血小板低下以及肝功能異常。骨髓穿刺檢查排除血液腫瘤疾患。血清學檢查排除病毒感染。病理切片檢查顯示脂肪層有明顯之發炎細胞浸潤和組織細胞之增生,以及紅血球被吞噬的情形。患者在接受類固醇治療下,於三到四週後康復。該患者之臨床表現和檢查結果符合一細胞吞噬性組織細胞性脂層炎,病程短且為良性,我們在此提出病例報告以及文獻回顧。 |
英文摘要 | Recently, we evaluated a 4-year-old boy with fever, abdominal pain and multiple reddish blue subcutaneous nodules of the low back and the extremities, especially of the lower legs for 10 days. Laboratory studies showed leukocytosis, thrombocytopenia and liver dysfunction. The bone marrow aspiration excluded a proliferative disease of the haematopoietic or lymphatic system. Serological tests excluded virus infections. In the histopathologic examination of skin biopsy, there was an intense inflammatory infiltration of the adipose tissue and proliferation of histiocytes with haemophagocytosis. The emption resolved within 3 to 4 weeks using the corticosteroid therapy. The symptoms and examinations of this patient were consistent with cytophagic histiocytic panniculitis. This case had a short and benign course. We report here a case presentation and a review of the literatures. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。