Image diagnoses for "Skin defects (superficially, deep)"
187 results with 477 images

Pemphigus vulgaris: extensive, painful erosions on the soft and hard palate

Pemphigus vulgaris. multiple, chronic, since 3 years intermittent, symmetric, trunk-accentuated, easily injured, flaccid, 0.2-3.0 cm large, red blisters confluent to larger, weeping and crusty areas. infestation of the oral mucosa.

pemphigus vulgaris: recurrent clinical picture for months. superficially, weeping, non-detachable (because painful) crusts are found on weeping surfaces. no clinically detectable blisters. at the same time, extensive erosions of the oral mucosa. on searching inspection of the skin, very isolated, easily injured (immediately bursting) blisters can be found (here in this picture on the patient's left shoulder)

Porphyria cutanea tarda: typical indication of a porphyria cutanea tarda; a banal trauma leads to a exfoliating injury of the traumatized area.

Porphyria cutanea tarda: close-up. older scars marked by stars. vertical arrows: encrusted erosions after traumta; vertical arrows: bulging (subepithelial - the entire epidermis forms the firm bladder roof) fresh areactive blisters (the blisters appear as if from nowhere. no signs of inflammation!)

Porphyria cutanea tarda: detailed picture; the variety of skin lesions can be reduced to certain features by careful analysis.

Porphyria cutana tarda. extensive traumatically induced erosions, flat ulcerations and older and fresh scarring. see further analyses.

Porphyria cutana tarda. extensive traumatically induced erosions, flat ulcerations and older and fresh scarring. onycholysis of the ring fingernail.

Pyoderma gangaenosum : Chronic, since more than 1 year progressive, large, flat, barely purulent ulcer with rounded, raised edges; sequence of images under immunosuppressive therapy in a six-month period

Pyoderma gangraenosum with multiple foci: Known, long-term immunosuppressive basic disease.

Pyoderma gangraenosum with multiple foci: Known immunosuppressive basic disease

Pyoderma gangraenosum. multiple, chronically progressive, painful, large-area, blue-reddish nodules, partly with polycyclic ulcerations. characteristic is the necrotic ulcer with a painful marginal zone with walllike, undermined margins and dark red, livid erythematous border.

Pyoderma gangraenosum: progressive, painful ulcer that has been present for several months in patients with known MGUS

Pyoderma gangraenosum: deep, painful ulcer that has existed for several months; ulcerative colitis ulcerosa that is located at the base of the tract.

severe zoster ophthalmicus. right-sided headache increasing for 5 days with accompanying feeling of illness. redness and swelling of the skin with stabbing, shooting pain for 3 days. extensive erythema and swelling. skin is highly sensitive to touch. no fever. no leukocytosis.

zoster. right sided headache with accompanying feeling of illness, increasing for 5 days. redness and swelling of the skin with stabbing, shooting pain for 3 days. extensive erythema and swelling. skin is highly sensitive to touch. no fever. no leukocytosis.

Calcinosis (cutis) dystrophica: Cause could not be clarified.

Erythema multiforme: suddenly occurring, itchy, disseminated exanthema with cocard-like plaques which has been present for 4 days. here the finding on the lower leg. striated arrangement after external stimulus. s. isomorphism (Koebner phenomenon).

Lymphoma cutaneous NK/T-cell lymphoma nasal type: ulcer covered with red granulation tissue and crusts that has been expanding for months with partial destruction of the nasal septum.

Leishmaniasis, cutaneous: about 8 weeks old, furuncoloid, moderately pressure dolent, red, rough lump with extensive central ulceration; history of previous vacation in Egypt; no systemic complaints.

Leishmaniasis cutane: after a holiday in Tunisia appeared, little symptomatic, roundish, red-brown ulcerated nodules.

Primary cutaneous CD30-positive large cell T-cell lymphoma: lymphoma known for alonger period of time with a faster growth tendency in recent months.

Porphyria cutana tarda: discrete finding with which the disease initially presents itself. after banal traumas subclinical blisters develop. here residuals with erosions and shallow ulcerations

Sézary syndrome: severe final febrile developmental stage. universal redness of the skin with extensive skin detachment. generalized lymphadenopathy, leukemic lymphocytic (CD4+) blood count (75-year-old female patient.

Erythema induratum (Nodular vasculitis): The 48-year-old patient has been suffering for 2 years from these intermittent, moderately painful, therapy-resistant plaques which tend to ulceration.