
Idiopathic guttate hypomelanosis L81.5
Hypomelanosis guttata idiopathica. multiple, 0.2-0.4 cm large, round, symptomless, white, slightly rough spots, persisting for months/years. DD: Stuccokeratoses

Idiopathic guttate hypomelanosis L81.5
Hypomelanosis guttata idiopathica: Disseminated, different sized, roundish, sharply defined, white patches on the lower leg of a 74-year-old patient; slight lesional scaling; solar lentigines.

Flash lamps
Flashlamps (side effects of the therapy): streaky hypopigmentation after IPL depilation, hair growth unchanged

Extrinsic skin aging L98.8
Chronic actinic damage to the skin: brown colouring of the leather-like thickened skin with splashes of depigmentation.

Klippel-trénaunay syndrome Q87.2
Klippel-Trénaunay syndrome. Extensive nevus flammeus; so far no evidence of soft tissue hypertrophy. No pelvic obliquity!

Vasculitis leukocytoclastic (non-iga-associated) D69.0; M31.0
Vasculitis leukocytoclastic (non-IgA-associated): multiple, since about 1 week existing, localized on both lower legs, irregularly distributed, 0.1-0.2 cm large, confluent in places, symptomless, red, smooth spots (not compressible).

Asymmetrical nevus flammeus Q82.5
Naevus flammeus: congenital, bilateral, chronically inpatient, bizarre, asymptomatic, non-syndromal naevus flammeus with livedo-like aspect

Ecchymosis syndrome, painful R23.8
Ecchymosis syndrome, painful seti 6 months of recurrent, painful, extensive skin bleeding on the abodes and extremities in an otherwise healthy 69-year-old female patient

Hyperpigmentation postinflammatory L81.0

Granulomatosis disciformis chronica et progressiva L92.1
Granulomatosis disciformis chronica et progressiva: Large, hyperpigmented, borderline infiltrated foci with atrophic surface.