Pigmented progressive purpuric dermatosis - Dermatose Purpúrica Progressiva Pigmentada
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Nos resultados do Stiftung Warentest de 2022 da Alemanha, a satisfação do consumidor com o ModelDerm foi apenas ligeiramente inferior do que com as consultas pagas de telemedicina.
Nos resultados do Stiftung Warentest de 2022 da Alemanha, a satisfação do consumidor com o ModelDerm foi apenas ligeiramente inferior do que com as consultas pagas de telemedicina.
relevance score : -100.0%
ReferencesPigmented purpuric dermatoses (PPD) são um grupo de doenças de pele caracterizadas por pequenas áreas de sangramento subcutâneo decorrentes de inflamação capilar. O PPD geralmente inicia‑se como manchas vermelhas a roxas, que posteriormente tornam‑se marrom‑douradas à medida que a hemossiderina é reabsorvida.
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 é o tipo mais comum de pigmented purpuric dermatoses (PPDs), que são doenças crônicas da pele caracterizadas por pequenas manchas vermelhas ou roxas e aumento da coloração da pele (manchas marrons, vermelhas ou amarelas). Os PPDs são classificados em cinco tipos: Schamberg's purpura, Majocchi purpura, lichen aureus, Gougerot‑Blum purpura e eczematoid‑like purpura of Doucas and Kapetanakis. Schamberg disease (SD) também é conhecido como progressive pigmentary dermatosis of Schamberg, purpura pigmentosa progressiva e Schamberg's purpura. Afeta principalmente homens e costuma aparecer na parte inferior das pernas, mas pode também ocorrer nas coxas, nádegas, tronco ou braços.
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.
Foram analisadas informações de 113 pacientes com DPP, incluindo 38 que foram submetidos à biópsia de pele para este estudo. O tipo clínico mais comum foi a doença de Schamberg (60,5%). Outras condições paralelas à DPP foram hipertensão (15,8%), diabetes (10,5%) e outras. Os históricos de medicação revelaram estatinas (13,2%), betabloqueadores (10,5%) e outros. Os possíveis fatores ligados à DPP incluíram infecção recente do trato respiratório superior (5,3%), permanência prolongada em pé, levando a pressão ortostática elevada (2,6%) e exercícios extenuantes (2,6%). O tratamento foi administrado a 36 pacientes (94,7%): oral antihistamines, pentoxifylline, topical steroids e/ou 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.
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.
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