
Varice reticular I83.91

Purpura pigmentosa progressive L81.7
Purpura eczematide-like purpura: non-symptomatic (no itching) "eczema-like" disease that has been recurrent for months in a completely healthy patient (no history of medication).

Vasculitis leukocytoclastic (non-iga-associated) D69.0; M31.0
vasculitis, leukocytoclastic (non-IgA-associated). multiple, acute, symmetric, localized on both legs for 2 weeks, symptomless, red, smooth spots and plaques. localized aspect of erythema multiforme.

Maculopapular cutaneous mastocytosis Q82.2
Urticaria pigmentosa (systemic mastocytosis): spots of varying size, disseminated, flat, oval or round, brownish-red spots on the trunk, buttocks and thighs; continuous proliferation of the spots for years; laboratory and histological evidence of systemic infestation.

Vasculitis (overview) L95.8

Acrodermatitis chronica atrophicans L90.4
Acrodermatitis chronica atrophicans. general view: blurred, livid red, spots on the right thigh extending to the hip and groin. no symptoms.

Purpura pigmentosa progressive L81.7
Purpura pigmentosa progressiva. reflected light microscopy, blurred, yellowish-brownish spots (haemosiderin) next to punctiform, fresh bleedings.

Granulomatosis disciformis chronica et progressiva L92.1
Granulomatosis disciformis chronica et progressiva: solitary, non-infiltrated, polycyclically limited, brown, symptomless, slow-growing spot.

Unilateral naevoid telangiectasia syndrome I78.8

Vasculitis leukocytoclastic (non-iga-associated) D69.0; M31.0

Granulomatosis disciformis chronica et progressiva L92.1
Granulomatosis disciformis chronica et progressiva. single, hardly infiltrated, hyperpigmented, bizarrely limited focus (only palpable as a spot) in the area of the lower leg.

Livedo racemosa (overview) M30.8
Livedo racemosa : irregular, bizarre non-closed circle segments, as pioneering morphological indicators of livedo racemosa, and cholesterol embolism occurred in this 73-year-old passon smoker.

Acrocyanosis I73.81; R23.0;
Acrocyanosis, livid discoloration of the lower extremity, here with pronounced onychomycosis.

Idiopathic guttate hypomelanosis L81.5
Hypomelanosis guttata idiopathica: Multiple, chronic, for years increasing, disseminated, mainly at the light exposed areas, preferably localized on the stretching side, 0.2-0.4 cm large, round, symptomless, white, slightly rough spots.

Acrocyanosis I73.81; R23.0;
acrocyanosis: typical picture of the red, cold foot in a 42-year-old chain smoker. variable course. erythema not painful. occurs at an ambient temperature of 20ºC and less. also in stressful situations

Livedoid vasculopathy L95.0
Livedovasculopathy: changes in the sole of the foot (rather rare localization)

Maculopapular cutaneous mastocytosis Q82.2
Urticaria pigmentosa:differently sized, disseminated, flat, oval or round, brownish-red spots on the trunk, buttocks and thighs; 52-year-old female patient. Continuous proliferation of the spots for years. No evidence of systemic infestation.

Ecchymosis syndrome, painful R23.8
Ecchymosis syndrome, painful. intermittent manifestation of painful skin bleeding in a 52-year-old manic-depressive woman. Initial development of edematous, overheated, pressure-sensitive erythema, followed by development of bleeding and slow expansion of the skin changes.

Klippel-trénaunay syndrome Q87.2
Klippel-Trénaunay syndrome: extensive, bilateral vascular malformation of capillary (naevus flammeus) and venous vessels (varicosis with chronic venous insufficiency - CVI); distinct soft tissue hypertrophy on the left side; no pelvic obliquity!

Striae cutis distensae L90.6

Acromegaly E22.0
Acromegaly: 43-year-old patient with known acromegaly. Noticeable increase in size of the lower extremities. Simultaneous development of excessive varicosis with consecutive chronic venous insufficiency (CVI).