- 期刊
Atrophoderma of Pasimi and Pierini-A Variant of Mouphea -Report of a Case and Review of the Literature-
Pasini與Pierini氏皮萎症─局限性鞏皮症之變異型 ─病例報告及文獻回顧─
摘要
Pasini與Pierini氏皮萎症是一種罕見但極具臨床特徵的疾病，典型皮膚病灶為境界鮮明、稍微下陷並帶有石灰色或棕色的斑，病人通常無自覺症狀，且病灶常雙側對稱出現。我們報告一例15歲女孩，最近3年來在其左側手臂及背部出現數個呈帶狀排列、稍微下陷的棕色斑。我們在其左側腰部進行皮膚切片，取下的組織包括正常皮膚與下陷部位，病理檢查發現在真皮深處局部有膠原纖維增厚及均質化的現象，因此我們診斷其為Pasini與Pierini氏皮萎症。
關鍵字
無資料並列摘要
Atrophoderma of Pasini and Pierini (APP) is a rare but clinically distinct skin disease characterized by sharply demarcated, slightly depressed patches with a slate-gray or brown color. The lesions are usually asymptomatic, bilateral and symmetrical. We report a 15-year-old girl who had a 3-year history of unilateral band-form, brownish, slightly depressed patches over the left arm and back. A skin biopsy from the left flank lesion including clinically normal skin and a depressed area was performed. The histopathologic study revealed thickening of the collagen fibers with homogenization in focal areas of reticular dermis at the lesion site, which is consistent with APP.
延伸閱讀
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- 陳振武、吳明彰（1980）。Pimaricin對Fusarium角膜真菌症之著效－病例報告。中華民國眼科醫學會雜誌，19()，149-153。https://doi.org/10.30048/ACTASOS.198005.0022