Poikilodermahttps://en.wikipedia.org/wiki/Poikiloderma
Poikiloderma waa xaalad maqaarka ah oo ka kooban meelaha midab‑dhac (hypopigmentation), midab‑kordhin (hyperpigmentation), dilac xididdada dhiigga (telangiectasias) iyo hoos u dhac (atrophy). Poikiloderma ayaa inta badan lagu arkaa laabta ama qoorta, oo lagu garto midabka cas ee maqaarka kaas oo inta badan lala xiriiriyo dhaawaca qorraxda.

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      References Diagnosis and Differential Diagnosis of Poikiloderma of Civatte: A Dermoscopy Cohort Study 36892344 
      NIH
      Poikiloderma of Civatte waa xaalad maqaarka ah oo caadi ah oo inta badan ka soo baxda qoorta iyo wejiga, gaar ahaan kuwa maqaarkoodu cad‑cad yahay, dumarka ka dambeeya caadada. Waxay u muuqataa isku dhafka telangiectasias, hyperpigmentation, iyo atrophy. Caadi ahaan, waxay saamaysaa meelaha qorraxda u soo ban‑baxa, sida wejiga, qoorta, iyo laabta, laakiin ma aha meelaha hadhsan. Poikiloderma of Civatte waxaa loo kala saari karaa iyadoo lagu salaynayo astaamihiisa ugu waaweyn: erythema, hyperpigmentation, ama isku dhafka labadaba. Sababta saxda ah si buuxda looma fahmin, laakiin arrimaha sida soo‑gaadhista qorraxda, isbeddelada hormoonnada, contact sensitization ama waxyaalaha la isku qurxiyo, iyo gabowga ayaa loo malaynayaa inay door ka ciyaaraan. Poikiloderma of Civatte waxay u egtahay inay si tartiib‑tartib ah uga sii darto waqti ka dib.
      Poikiloderma of Civatte (PC) is a rather common benign dermatosis of the neck and face, mainly affecting fair-skinned individuals, especially postmenopausal females. It is characterized by a combination of a reticular pattern of linear telangiectasia, mottled hyperpigmentation and superficial atrophy. Clinically, it involves symmetrically sun-exposed areas of the face, the neck, and the V-shaped area of the chest, invariably sparing the anatomically shaded areas. Depending on the prevalent clinical feature, PC can be classified into erythemato-telangiectatic, pigmented, and mixed clinical types. The etiopathogenesis of PC is incompletely understood. Exposure to ultraviolet radiation, hormonal changes of menopause, contact sensitization to perfumes and cosmetics, and normal ageing have been incriminated. The diagnosis is usually clinical and can be confirmed by histology, which is characteristic, but not pathognomonic. The course is slowly progressive and irreversible, often causing significant cosmetic disfigurement.