Zobrazeno 1 - 10
of 56
pro vyhledávání: '"K E, Greer"'
Publikováno v:
Journal of the American Academy of Dermatology. 44:725-746
Sarcoidosis is a systemic noncaseating granulomatous disorder of unknown origin. The cutaneous manifestations of sarcoidosis often enable the dermatologist to be the first physician to make the diagnosis. This article reviews essential sarcoidosis pa
Autor:
K A, Knoell, K E, Greer
Publikováno v:
Pediatrics in Review. 20:46-52
Publikováno v:
Dermatology online journal. 19(8)
Numerous medications have been associated with the development of subacute cutaneous lupus erythematosus. A mechanism explaining how unrelated drug classes can lead to subacute cutaneous lupus erythematosus has remained elusive, suggesting that there
Autor:
N A, Levin, K E, Greer
Publikováno v:
Dermatology nursing. 13(3)
Endocrine disorders such as diabetes or Cushing's syndrome often have cutaneous findings, including changes to the skin, hair, and nails. In this review, the major causes, clinical manifestations, laboratory workup, and treatment of the most importan
Autor:
N A, Levin, K E, Greer
Publikováno v:
Cutis. 66(1)
For centuries, scurvy, or vitamin C deficiency, decimated crews of sailing ships on long sea voyages and populations deprived of fresh fruits and vegetables during times of war or famine. Today, scurvy is extremely rare in the United States, and its
Publikováno v:
Journal of cutaneous pathology. 27(1)
Lipedematous alopecia is a rare condition of unknown etiology characterized by a thick, boggy scalp with varying degrees of hair loss that occurs in adult black females, with no clearly associated medical or physiologic conditions. The fundamental pa
Publikováno v:
Archives of dermatology. 133(8)
Dysplastic melanocytic nevi (DMN) are thought to represent a clinical and histologic bridge between common pigmented nevi and superficial spreading malignant melanoma. The following clinical criteria for DMN were established to aid in the proper iden
Autor:
J D, Hendrix, K E, Greer
Publikováno v:
Cutis. 57(5)
A single case of Rubinstein-Taybi syndrome associated with numerous giant keloids is reported. The patient manifested all the major features of Rubinstein-Taybi syndrome. The cause of this multisystem developmental disorder is unknown.
Autor:
D M, Elder, K E, Greer
Publikováno v:
Geriatrics. 50(8)
Venous disease accounts for up to 90% of all cases of chronic leg ulcers. Patients with venous disease have relatively unhealthy, ischemic tissue in the lower legs, and slight trauma often initiates an ulcer. Symptoms include leg swelling, which is o
Publikováno v:
Cutis. 55(3)
Papular mucinosis, also known as lichen myxedematosus, is a rare, idiopathic disorder in which focal deposits of mucin accumulate in the dermis. It has been previously reported in two patients with human immunodeficiency virus infection; we describe