Malformations, vascular: mixedvenous/capillary malformation with a large, subcutaneous venous part; here in a lateral view where the clear protrusion of the neck contour is visible.
Dupuytren's contracture: Severity III: Nodular induration of the palm with retraction of the skin and incipient flexion contracture of the ring finger.
Circumscribed scleroderma. Atrophy of the right leg muscles, atrophy of the gluteal muscles on the right, shortening of the right leg (difference 2.0 cm) with consecutive secondary pelvic obliquity and scoliosis in a 19-year-old female patient. Multiple white indurated plaques on the right leg are also present on the thighs, lower legs and in the foot area.
Fibromatosis, digital infantile. detailed enlargement of the findings of the right big toe of the above mentioned patient. 2 very rough, in the center somewhat yellowish, reddened nodes at the margins are impressive.
Behçet, M.. Distinct swelling of the right upper lip in a 70-year-old woman. Intraorally, in the region of the right upper lip, aphtae measuring about 5 mm. For about six to seven years recurrent, relapsing aphtae of the oral cavity.
Plantar fibromatosis: Chronic stationary, subcutaneously located, skin-coloured to brown, approx. 5 x 4 cm large, coarse knot of a 60-year-old man, localised at the Arcus plantaris. 10 years of pressure pain and difficulties in rolling.
Keratosis pilaris syndrome: Numerous follicularly bound papules in the area of the forearm in the sense of a keratosis follicularis in a 47-year-old female patient.
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).
Connective tissue nevus, lumbosacral. 30-year-old woman, in whom these changes had been present since earliest childhood. Clinically, in the sacral region, sharply defined, very firm, partly rubbery, slightly raised above the skin level, cobblestone-like arranged, whitish papules and plaques with smooth surface are found. Localization and clinic are characteristic for the diagnosis. Secondary findings are angiofibromas in the face.
Hidrocystoma, apocrine. remark: solitary cysts of the lid margin are rather evaluated as apocrine cysts, but histological differentiation is often not possible (see also Hidrocystoma, eccrine)
Pronounced livedo racemosa: Intermediate findings after 2 more years (period of clinical follow-up over a period of 8 years); extensive scar healing after therapy with high-dose venous immunoglobulin therapy (IVIG)
Scleroedema adultorum. extensive, board-like induration in the area of the upper back and neck. there is still a discreet erythema. the skin is not compressible and cannot be wrinkled.
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