Image diagnoses for "Nodule (<1cm)"
255 results with 972 images

Type I neurofibromatosis, peripheral type or classic cutaneous form. massive tumorous transformation of the skin with numerous generalized distributed, soft, skin-colored, partly pointed conical shaped neurofibromas on the left mamma. the CT examination (skull) did not reveal any pathological findings. no neurofibromas known in the family.

Mycosis fungoides advanced tumor stage: since years known Mycosis fungoides. advanced tumor stage. findings of the same patient in 2017

Endemic Kaposisarcoma, reddish-livid plaques around the edges of the foot in elderly patients.

Type I Neurofibromatosis, peripheral type or classic cutaneous form. Since puberty slowly increasing formation of these soft, skin-coloured or slightly brownish, painless papules and nodules. Several café-au-lait spots.

Cylindrome. 72-year-old female patient with familial multiple Cylindromas (Brooke-Spiegler syndrome). Differently large aggregated papules interspersed with telangiectasias and smooth nodules in the region of the temple.

Merkel cell carcinoma. Metastatic tumor.

Lip carcinoma: Apparently from the skin of the lips (not from the lip red) spreading to the lip red, grown within 6 months, firm, painless, broadly based knot with central honeycomb plug.

Numerous keloids and hypertrophic scars, after acne vulgaris has largely healed.

Detailed view: The diagnosis "pigmented basal cell carcinoma" is visible at the left margin, where the spatter-like hyperpigmentation is found (accumulation of melanin clods in the tumor parenchyma, caused by the "accompanying proliferation" of melanocytes). At the upper pole local tumor decay and ulceration.

acne papulopustulosa

Acne conglobata: with accompanying severe acne inversa with extensive scarring induration of the entire axilla as well as strand-like scars which have led to a restriction of mobility in the shoulder joint.

Angiosarcoma of the head and facial skin. slow, chronic progression without subjective complaints. initially contusiform, blue-red discolored skin, later angiomatous nodules and the development of multiple satellite metastases.

Boils. 38-year-old patient with recurrent boils. 2.5 x 2.0 cm large, spontaneously formed, pressure-marked, flat raised lump with yellow necrotic tip and scaly crown.

Keratosis seborrhoeic (papillomatous type); unusual localization of this solitary, completely asymptomatic benign tumor.

Leishmaniasis (mucocutaneous leishmaniasis of the old world): Ethiopian (HIV-infected) patient with skin and mucous membrane infestation

Myzetome: Indolent, chronic granulomatous infection of the skin and subcutis with circumscribed, pseudotumorous swellings and fistula formation ("Madura foot").

Atheroma Chronic stationary, growing imperceptibly for more than 10 years, solitary, sharply defined, on the base well movable, indolent, plumply elastic, about 5.0 cm large, skin-colored, smooth lump.

type i neurofibromatosis, peripheral type or classic cutaneous form. numerous smaller and larger soft papules and aques. several café-au-lait spots.

Amelanotic acrolentiginous malignant melanoma: slowly growing nodule known for several years; increasing nail destruction in the last six months, also weeping and bleeding, sometimes slight pain; encircled and marked with an arrow, deep-seated pigment remains, which suggest the diagnosis "malignant melanoma".