Pigmented progressive purpuric dermatosishttps://en.wikipedia.org/wiki/Pigmented_purpuric_dermatosis
Tagraíonn Pigmented progressive purpuric dermatosis do na coinníollacha craiceann neamh-itching arb iad is sainairíonna brúchtaí craiceann purpuric. Tá méid an lesion ó 0.3 go 1 cm agus is minic a fheictear iad sna foircinn níos ísle. Cabhróidh an uachtar cortisone leis an itching agus feabhas a chur ar mhílí an chraiceann. Níl aon chomharthaí eile mar thoradh ar pigmented progressive purpuric dermatosis in aice le dídhathú craicinn. Is iad na loit is minice ar na géaga níos ísle, ach d'fhéadfadh tarlú áit ar bith ar an gcomhlacht, lena n-áirítear na lámha, airm, torso agus fiú an muineál.

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  • Schamberg disease ― fireannach 26 bliain d'aois le paiste de lí asymptomatic agus telangiectasia ar an cos.
    References Pigmented Purpuric Dermatoses: A Complete Narrative Review 34070260 
    NIH
    Is grúpa coinníollacha craiceann iad Pigmented purpuric dermatoses (PPD) atá marcáilte ag réimsí beaga fuilithe faoin gcraiceann de bharr athlasadh ribeach. Is gnách go dtosaíonn PPD chomh dearg le spotaí corcra a iompaíonn níos déanaí órdhonn de réir mar a athionsúnnaítear an hemosiderin.
    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 32809367 
    NIH
    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.
     Characteristics and Clinical Manifestations of Pigmented Purpuric Dermatosis 26273156 
    NIH
    Rinneadh anailís ar fhaisnéis ar 113 othar le PPD, lena n-áirítear 38 a chuaigh faoi bhithóipse craicinn don staidéar seo. Ba é an cineál cliniciúil is coitianta ná galar Schamberg (60. 5%) . I measc na gcoinníollacha eile taobh le PPD bhí Hipirtheannas (15. 8%) , diaibéiteas (10. 5%) , agus daoine eile. Nocht stair cógas statins (13. 2%) , bacóirí béite (10. 5%) , agus daoine eile. I measc na bhfachtóirí féideartha a bhaineann le PPD bhí ionfhabhtú riospráide uachtarach le déanaí (5. 3%) , seasamh fada as a dtagann brú ard ortastatach (2. 6%) , agus aclaíocht dhian (2. 6%) . Tugadh cóireáil do 36 othar (94. 7%) - 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.