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A dermatomycosis is a skin disease caused by a fungus. [1] The most frequent form is dermatophytosis (ringworm, tinea). Another example is cutaneous candidiasis. These fungal infections impair superficial layers of the skin, hair and nails.
Lymphedema is most frequently a complication of cancer treatment or parasitic infections, but it can also be seen in a number of genetic disorders. Tissues with lymphedema are at high risk of infection because the lymphatic system has been compromised. [3] Though incurable and progressive, a number of treatments may improve symptoms. [2]
Tinea versicolor (also known as dermatomycosis furfuracea, pityriasis versicolor, and tinea flava) [2] is a condition characterized by a skin eruption on the trunk and proximal extremities, hypopigmentation macule in area of sun induced pigmentation. During the winter the pigment becomes reddish brown.
Treatment is generally performed using antifungal medicines, usually in the form of a cream or by mouth or injection, depending on the specific infection and its extent. [15] Some require surgically cutting out infected tissue. [3] Fungal infections have a world-wide distribution and are common, affecting more than one billion people every year ...
Numerous studies have found Tinea capitis to be the most prevalent dermatophyte to infect children across the continent of Africa. [32] Dermatophytosis has been found to be most prevalent in children ages 4 to 11, infecting more males than females. [32] Low socioeconomic status was found to be a risk factor for Tinea capitis. [32]
Primary lymphedema is a form of lymphedema which is not directly attributable to another medical condition. It can be divided into three forms, depending upon age of onset: congenital lymphedema, lymphedema praecox, and lymphedema tarda. [1] Congenital lymphedema presents at birth. Lymphedema praecox presents from ages 1 to 35.
Milroy's disease is also known as primary or hereditary lymphedema type 1A or early onset lymphedema. It is a very rare disease with only about 200 cases reported in the medical literature. Milroy's disease is an autosomal dominant condition caused by a mutation in the FLT4 gene which encodes the vascular endothelial growth factor receptor 3 ...
Treatment for lymphedema includes compressing fluid out of her arms and wearing a custom-fitted compression sleeve to avoid aggravating the swelling while doing normal tasks or ingesting things ...