Pigmented progressive purpuric dermatosis - 色素性紫斑病
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ドイツの2022年Stiftung Warentestの結果では、ModelDermに対する消費者満足度は有料の遠隔医療相談よりもわずかに低いだけでした。
ドイツの2022年Stiftung Warentestの結果では、ModelDermに対する消費者満足度は有料の遠隔医療相談よりもわずかに低いだけでした。
relevance score : -100.0%
ReferencesPigmented purpuric dermatoses (PPD) は、毛細血管の炎症による皮膚下の小さな領域での出血を特徴とする一連の皮膚疾患です。PPD は通常、赤から紫の斑点として始まり、ヘモジデリンが再吸収されるにつれて金茶色に変化します。
Pigmented purpuric dermatoses (PPD) include several skin diseases characterized by multiple petechial hemorrhage as consequence of capillaritis. PPD generally present with red to purple macules that progressively evolve to golden-brown color as the hemosiderin is reabsorbed.
Pigmented purpuric dermatoses (PPD) include several skin diseases characterized by multiple petechial hemorrhage as consequence of capillaritis. PPD generally present with red to purple macules that progressively evolve to golden-brown color as the hemosiderin is reabsorbed.
Schamberg disease は pigmented purpuric dermatoses (PPDs) の最も一般的なタイプで、小さな赤または紫の斑点と、皮膚の色素沈着（茶色、赤、または黄色の斑点）がみられる慢性皮膚疾患です。PPD は、Schamberg's purpura、Majocchi purpura、lichen aureus、Gougerot‑Blum purpura、eczematoid‑like purpura of Doucas and Kapetanakis の5つのタイプに分類されます。Schamberg disease (SD) は progressive pigmentary dermatosis of Schamberg、purpura pigmentosa progressiva、Schamberg's purpura とも呼ばれます。主に男性に発症し、通常は下腿に現れますが、太もも、臀部、胴体、腕にも出現することがあります。
Schamberg disease represents the most common type of pigmented purpuric dermatoses (PPDs), a chronic, benign, cutaneous eruptions characterized by petechiae, purpura, and increased skin pigmentation (brown, red, or yellow patchy). The PPDs are grouped into five clinical entities: Schamberg's purpura, Majocchi purpura, lichen aureus, Gougerot-Blum purpura and, eczematoid-like purpura of Doucas and Kapetanakis. Schamber disease (SD) has also been called: progressive pigmentary dermatosis of Schamberg, purpura pigmentosa progressive and, Schamberg's purpura. It is commonly seen in males and mainly affects the tibial regions, and could involve thighs, buttocks, trunk, or upper extremities.
Schamberg disease represents the most common type of pigmented purpuric dermatoses (PPDs), a chronic, benign, cutaneous eruptions characterized by petechiae, purpura, and increased skin pigmentation (brown, red, or yellow patchy). The PPDs are grouped into five clinical entities: Schamberg's purpura, Majocchi purpura, lichen aureus, Gougerot-Blum purpura and, eczematoid-like purpura of Doucas and Kapetanakis. Schamber disease (SD) has also been called: progressive pigmentary dermatosis of Schamberg, purpura pigmentosa progressive and, Schamberg's purpura. It is commonly seen in males and mainly affects the tibial regions, and could involve thighs, buttocks, trunk, or upper extremities.
この研究では、皮膚生検を受けた38人を含む113人のPPD患者の情報を分析しました。最も一般的な臨床型はシャンベルグ病（60.5%）でした。PPDと併存する主な合併症は、高血圧（15.8%）や糖尿病（10.5%）などです。投薬歴では、スタチン（13.2%）やベータ遮断薬（10.5%）が確認されました。PPDに関連する可能性のある要因として、最近の上気道感染症（5.3%）、長時間の立位による起立性血圧上昇（2.6%）、激しい運動（2.6%）が挙げられます。治療は36人の患者（94.7%）に実施され、口腔抗ヒスタミン薬（oral antihistamines）、ペントキシフィリン（pentoxifylline）、外用ステロイド（topical steroids）、および/または光線療法（phototherapy）などが用いられました。
Information on 113 patients with PPD was analyzed, and 38 subjects with skin biopsy were included for this study. Schamberg's disease was the most frequent clinical type (60.5%). Concomitant diseases included hypertension (15.8%), diabetes (10.5%), and others. Associated medication histories included statins (13.2%), beta blockers (10.5%), and others. Possibly associated etiologic factors were recent upper respiratory infection (5.3%), high orthostatic pressure due to prolonged standing (2.6%), and strenuous exercise (2.6%). A total of 36 patients (94.7%) were treated with one or more treatment methods, including oral antihistamines, pentoxifylline, topical steroids, and/or phototherapy.
Information on 113 patients with PPD was analyzed, and 38 subjects with skin biopsy were included for this study. Schamberg's disease was the most frequent clinical type (60.5%). Concomitant diseases included hypertension (15.8%), diabetes (10.5%), and others. Associated medication histories included statins (13.2%), beta blockers (10.5%), and others. Possibly associated etiologic factors were recent upper respiratory infection (5.3%), high orthostatic pressure due to prolonged standing (2.6%), and strenuous exercise (2.6%). A total of 36 patients (94.7%) were treated with one or more treatment methods, including oral antihistamines, pentoxifylline, topical steroids, and/or phototherapy.
色素性紫斑病 (Pigmented progressive purpuric dermatosis) は、皮膚の変色以外に症状を伴いません。この病変は下肢に最も頻繁に現れますが、手・腕・胴体、さらには首など、体のあらゆる部位に出る可能性があります。
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