Image diagnoses for "red"
899 results with 4541 images

Parapsoriasis en plaques large-heart poikilodermatic: a sympothless, slowly progressive clinical picture that has existed for several years, with poikilodermatic changes consisting of reticular lichenoid, pityriasiform scaling, papules and plaques and central atrophy of the skin.

Scabies norvegica: excessive infestation with dirty-brown, keratotic changes in the area of the face.

Cheilitis simplex in Melkersson Rosenthal syndrome.

Dermatosis acute febrile neutrophils: Findings in the legs.

Candida granuloma. chronic recurrent nodular cutaneous-subcutaneously localized, deep-reaching, livid inflammatory foci on the wrist of an immunocompromised, 28-year-old patient. abundant C. albicans detectable in the smear. development of new nodules despite oral antimycotic medication. partial healing leaving post-inflammatory pigmentation.

Purpura pigmentosa progressiva: etiologically unexplained (medication?) pronounced clinical picture that has been changing for several months with symmetrically distributed, disseminated, non-itching, yellow-brown, spots.

Keratosis lichenoides chronica: generalized eminently chronic, moderately itchy clinical picture with reddish, firm, papules and plaques with scaling.

Ulcus cruris arteriosum: chronic, slowly progressive, painful, deep, sharp-edged ulcer located in the area of the lower leg clitoris, measuring approx. 5.5 x 3.5 cm. The periulcerous area is reddened and overheated. The patient suffers from a PAVK of the multi-level type and has been a heavy cigarette smoker for 30 years.

Balanitis plasmacellularis: chronic balanitis in a 62 year old patient. no other skin diseases known. no diabetes mellitus. slight urinary incontinence in case of prostate hyperplasia. sharply defined, slightly raised red plaque. no significant symptoms.

Lymphangioma circumscriptum: Densely aggregated vesicles, usually with haemorrhagic content (so-called haematolymphangioma).

Hand-foot-mouth disease. few, acute, painful, polygonal vesicles with a red courtyard. unspecific flu-like prodromies that had persisted about 2 weeks before.

Leiomyoma. Close up of the multiple leiomyomas described above.

Lichen sclerosus extragenitaler: Progressive lichen sclerosus for 2 years with a clearly sunken scarring of the lower lip and chin; surrounding, flat, blurred, clearly consistent plaque with a red-white coloration in the chin area (here the clinical features of the lichen sclerosus are visible).

Purpura thrombocytopenic: line shaped, fresh skin bleeding (diascopically not pushable away) after intensive scratching

Angioma seniles of the lips (also lip margin angioma): a soft, completely compressible, symptom-free lump that has existed for several years.

Psoriasis seborrhoeic type: Chronic recurrent, sharply defined, flat, rough, partly with yellowish scaling, bordering, red spots and plaques.

ecchymosis syndrome, painful, intermittent manifestation of painful skin bleeding in a 48-year-old man. initial development of oedematous, overheated, pressure-sensitive erythema. subsequent development of skin bleeding and slow expansion of the skin changes. scarless healing after 1-2 weeks. in the present case, there was a severely pronounced clinical picture with multiple accompanying symptoms, especially fever, weight loss, fatigue, muscle and headaches, arthralgia, epistaxis, haemoptysis and haematuria.

Dermatosis, acute febrile neutrophils (Sweet Syndrome): suddenly appearing inflammatory, succulent, livid red papules that have conflued into larger and plaques, combined with fever and feeling of illness.