Image diagnoses for "Arm/Hand"
352 results with
787 images
Results for Arm/Hand
Acrodermatitis chronica atrophicans L90.4
Acrodermatitis chronica atrophicans: Livid erythema on the back of the right hand and nail dystrophies in a 78-year-old female patient with confirmed neuroborreliosis 6 years ago. Cushion-like (pernion-like) plaques on the fingers. Persistent pain in the carpal and interphalangeal joints.
Acrodermatitis continua suppurativa L40.2
acrodermatitis continua suppurativa. complete destruction of the nail organ at the thumb end of the right hand of a 54-year-old patient. recurrent small yellowish blisters and pustules for approx. 4-5 years. considerable spontaneous and pressure pain in case of relapsing activities. no evidence of osseous destruction, no soft tissue calcification so far.
Acrodermatitis continua suppurativa L40.2
acrodermatitis continua suppurativa. persistent, therapy-resistant changes of the right thumb of a 68-year-old woman since 3 years. initially a suppuration at the medial nail bed was observed which became more and more severe and finally led to nail extraction. 2 further nail extractions followed after 2 recurrences. the nail matrix is distally detached and altogether dystrophic. in the distal region there is a smaller weeping plaque. secondary findings are a melanonychia striata as a central, dark, longitudinal stripe at the nail.
Acrodermatitis continua suppurativa L40.2
acrodermatitis continua suppurativa. chronic, red, rough plaques with recurrent pustular formation and onychodystrophies. pressure dolence. primary efflorescence (subcorneal pustules) and general symptoms are indicative. in the advanced course, acral skin and bone atrophies were observed in addition to the pronounced onychodystrophies.
Acrodermatitis continua suppurativa L40.2
Recurrent sterile pustular disease of theacromion, which tends to mutate and leads to atrophy and loss of nails if it occurs repeatedly and persists for a long time (see figure).
Gianotti-crosti syndrome L44.4
Punctured palmoplantar keratosis type 3 L85.8
Acrokeratoelastoidosis: In a band-shaped arrangement at the transition zone from field skin to groin skin lichenoid shiny, 0.1-0.2 cm large, polygonally limited, yellowish to skin-coloured, completely asymptomatic papules appear.
Acrocyanosis I73.81; R23.0;
acrocyanosis. acute, changeable, homogeneously laminar, reddish-livid skin discoloration with reduced temperature. doughy swelling, hyperhidrosis, perniones and cutis marmorata. sometimes slight pain and dysesthesia.
Acrocyanosis I73.81; R23.0;
Acrocyanosis in right heart failure in age-related atrophic, shiny skin with solar lentigines on the back of the hand (DD: chronic Lyme disease - picture of acrodermatitis chronica atrophicans).
Acrocyanosis I73.81; R23.0;
acrocyanosis in age-atrophied, shiny skin with half and half nails. DD: chronic lyme borreliosis. here the picture of acrodermatitis chronica atrophicans is present. the cold-dependence of the redness is not very pronounced. conspicuous (see stronger enlargement) the smooth atrophic skin surface. a positive borrelia serology is always to be expected in this stage of a borrelia infection.
Angiokeratoma circumscriptum D23.L
Angiokeratoma circumscriptum, large confluent angiokeratomas in the area of the foot with cavernous transformation.
Angiokeratoma circumscriptum D23.L
Angiokeratoma circumscriptum. 20-year-old female patient with a lesion composed of several types of efflorescence. The skin lesions present have existed since birth. The blue-black parts have gradually developed over the past five years. In addition to two-dimensional red spots (upper part), red papules (lower part) and blue-black bumped plaques with a smooth, shiny surface are found. Soft, spongy consistency in the centre.
Artifacts L98.1
Artifacts L98.1
Atrophy senile of the skin L90.8
Atrophy, senile: parchment-like, pale yellow skin with clearly protruding veins in the area of the back of the hand in the elderly patient.
Calcinosis cutis (overview) L94.2
Calcinosis dystrophica disseminated: reddened nodules with painful central ulcerations and visible calcifications; the changes occurred bilaterally in the underlying progressive systemic scleroderma.
Calcinosis cutis (overview) L94.2
Calcinosis cutis: ulceration with a rock-hard, irregular base and reddened periulcerous surroundings; more frequent, e.g. in systemic scleroderma
Melasma L81.1