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Prurigo nodularis (PN), also known as nodular prurigo, is a skin disorder characterized by pruritic , nodular lesions, which commonly appear on the trunk, arms and legs. [1] Patients often present with multiple excoriated nodules caused by chronic scratching.
Smaller (less than 0.5 cm) raised soft tissue bumps may be termed papules. [3] The evaluation of a skin nodule includes a description of its appearance, its location, how it feels to touch and any associated symptoms which may give clues to an underlying medical condition. [4] Nodules in skin include dermatofibroma [5] and pyogenic granuloma. [6]
Cutaneous lupus mucinosis, also known as papular and nodular mucinosis in lupus erythematosus, papular and nodular mucinosis of Gold, and papulonodular mucinosis in lupus erythematosus, is a cutaneous condition characterized by lesions that present as asymptomatic skin-colored, at times reddish, 0.5–2 cm papules and nodules. [1] [2]
Gianotti–Crosti syndrome (infantile papular acrodermatitis, papular acrodermatitis of childhood, papulovesicular acrolocated syndrome) Giant condyloma acuminatum (Buschke–Löwenstein tumor, giant condyloma of Buschke–Löwenstein tumor) Hand-foot-and-mouth disease; Heck's disease (focal epithelial hyperplasia) Hemorrhagic fever with renal ...
Acral persistent papular mucinosis (APPM) is a rare form of lichen myxedematosus. It is characterized by small papules on the backs of the hands, wrists, and extensor aspects of the distal forearms, with no further clinical or laboratory indications. Lesions tend to persist and may grow in number gradually.
Papular mucinosis (also known as scleromyxedema, [1] [2] "generalized lichen myxedematosus" and "sclerodermoid lichen myxedematosus") is a rare skin disease. Localized and disseminated cases are called papular mucinosis or lichen myxedematosus while generalized, confluent papular forms with sclerosis are called scleromyxedema.
papules or nodules which are red, globular and non-blanching, with a vascular appearance; purplish nodules sufficiently similar to Kaposi's sarcoma that a biopsy may be required to verify which of the two it is; a purplish lichenoid plaque; a subcutaneous nodule which may have ulceration, similar to a bacterial abscess
Progressive nodular histiocytosis is a cutaneous condition clinically characterized by the development of two types of skin lesions: superficial papules and deeper larger subcutaneous nodules. [ 1 ] : 718 Progressive nodular histiocytosis was first reported in 1978 by Taunton et al. [ 2 ] It is a subclass of non-Langerhans cell histiocytosis ...