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HIV-associated lipodystrophy commonly presents with fat loss in face, buttocks, arms and legs. [citation needed]There is also fat accumulation in various body parts. . Patients often present with "buffalo hump"-like fat deposits in their up
Lipodystrophy syndromes are a group of genetic or acquired disorders in which the body is unable to produce and maintain healthy fat tissue. [ 1 ] [ 2 ] The medical condition is characterized by abnormal or degenerative conditions of the body's adipose tissue .
The management of lipodermatosclerosis may include treating venous insufficiency with leg elevation and elastic compression stockings. [9] In some difficult cases, the condition may be improved with the additional use of the fibrinolytic agent, stanozol.
Cosmetic concerns may cause patients to refuse or stop treatment. If severe enough, the fat accumulation may result in sleep apnea or other sleep disorders, migraines, decreased range of motion, discomfort due to pressure on internal organs, and general loss of condition. Fat loss may result in pain in the buttocks when seated.
Lipedema was first identified in the United States, at the Mayo Clinic, in 1940. [ 32 ] [ 33 ] Most attribute the original identification of lipedema to E. A. Hines and L. E. Wold (1951). [ 32 ] Despite that, lipedema is barely known in the United States to physicians or to the patients who have the disease.
Lipoatrophy occurs in HIV-associated lipodystrophy, one cause of which is an adverse drug reaction that is associated with some antiretroviral medications. [ 2 ] A more general term for an abnormal or degenerative condition of the entire body's adipose tissue is lipodystrophy .
Even with anti-retroviral treatment, over the long term HIV-infected people may experience neurocognitive disorders, [219] osteoporosis, [220] neuropathy, [221] cancers, [222] [223] nephropathy, [224] and cardiovascular disease. [174] Some conditions, such as lipodystrophy, may be caused both by HIV and its treatment. [174]
Acquired generalized lipodystrophy (AGL), also known as Lawrence syndrome [1] and Lawrence–Seip syndrome, [1] is a rare skin condition that appears during childhood or adolescence, characterized by fat loss affecting large areas of the body, particularly the face, arms, and legs.