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Gianotti–Crosti syndrome (/ dʒ ə ˈ n ɒ t i ˈ k r ɔː s t i /), also known as infantile papular acrodermatitis, [1] papular acrodermatitis of childhood, [1] and papulovesicular acrolocated syndrome, [2]: 389 is a reaction of the skin to a viral infection. [3] Hepatitis B virus [4] and Epstein–Barr virus are the most frequently reported ...
All these rashes are made worse by exposure to sunlight, and are often very itchy, painful, and may bleed. [ 10 ] If a person exhibits only skin findings characteristic of DM, without weakness or abnormal muscle enzymes, then he or she may be experiencing amyopathic dermatomyositis (ADM), formerly known as "dermatomyositis sine myositis".
This is a shortened version of the thirteenth chapter of the ICD-9: Diseases of the Musculoskeletal System and Connective Tissue. It covers ICD codes 710 to 739. The full chapter can be found on pages 395 to 415 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1.
This is a shortened version of the twelfth chapter of the ICD-9: Diseases of the Skin and Subcutaneous Tissue. It covers ICD codes 680 to 709. The full chapter can be found on pages 379 to 393 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1.
A maculopapular rash is a type of rash characterized by a flat, red area on the skin that is covered with small confluent bumps. It may only appear red in lighter-skinned people. The term "maculopapular" is a compound: macules are small, flat discolored spots on the surface of the skin; and papules are small, raised bumps.
Lichen planus may be categorized as affecting mucosal or cutaneous surfaces.. Cutaneous forms are those affecting the skin, scalp, and nails. [10] [11] [12]Mucosal forms are those affecting the lining of the gastrointestinal tract (mouth, pharynx, esophagus, stomach, anus), larynx, and other mucosal surfaces including the genitals, peritoneum, ears, nose, bladder and conjunctiva of the eyes.
Systemic-onset juvenile idiopathic arthritis (sJIA), also known as Still disease, Still's disease, and systemic juvenile idiopathic arthritis, is a subtype of juvenile idiopathic arthritis (JIA) that is distinguished by arthritis, a characteristic erythematous skin rash, and remitting fever. [5]
The clinical manifestation of this group of disorders is chronic joint inflammation that results in pain, swelling, warm and stiffness of the joints that persistent for a long period of time. [10] General signs of childhood arthritis disorders include: Joints: Swollen, stiff, red, warm, and/or painful joints. [9]