Stevens-Johnson syndrome

[ste´venz jon´son] a severe and sometimes fatal form of erythema multiforme in which the lesions may involve the oral and anogenital mucosa, eyes, and viscera, associated with such constitutional symptoms as malaise, headache, fever, arthralgia, and conjunctivitis.

Ste·vens-John·son syn·drome

(stē'vĕnz jon'sŏn), a bullous form of erythema multiforme that may be extensive, involving the mucous membranes and large areas of the body; it may produce serious subjective symptoms and may have a fatal termination.
See also: ocular-mucous membrane syndrome. Synonym(s): erythema multiforme bullosum, erythema multiforme exudativum, erythema multiforme major

Ste·vens-John·son syn·drome

Stevens-Johnson syndrome

(stē′vənz-jŏn′sən)n. A severe inflammatory eruption of the skin and mucous membranes, usually occurring after an infection, with malignancy, or as an allergic reaction to drugs or other substances.

Stevens-Johnson syndrome

Dermatology A variant of erythema multiforme characterized by purpuric macules or atypical targetoid lesions with focal confluence and epithelial detachment covering < 10% of body surface;¹⁄₂ are reactions to drugs–eg, sulfonamides, anticonvulsants, allopurinol, etc; 10-30% are accompanied by systemic Sx Clinical Fever, erosive stomatitis, lesions of anogenital mucosa, conjunctiva–keratitis, corneal erosions, RTIs; < 5% are fatal Treatment Delete offending drug

Ste·vens-John·son syn·drome

(stē'vĕnz jon'sŏn sin'drōm) A bullous form of erythema multiforme that may be extensive, involving the mucous membranes and large areas of the body; it may produce serious subjective symptoms and may be fatal.

Stevens-Johnson syndrome

S18-899220 (ste'venz-jon'son) [Albert M. Stevens, 1884–1945, Frank C. Johnson, 1894–1934, U.S. pediatricians] STEVENS-JOHNSON SYNDROMEA systemic skin disease, probably identical to toxic epidermal necrolysis, that produces fevers and lesions of the oral, conjunctival, and vaginal mucous membranes. It is marked by a cutaneous rash that is often widespread and severe. Skin loss may lead to dehydration, infection, or death. See: illustration; erythema multiformeillustration

Stevens-Johnson syndrome

A rare but severe condition involving skin and MUCOUS MEMBRANES of the eyes, mouth, nose and genitals and featuring ulceration and loss of epithelium with abnormal adhesions. A form of ERYTHEMA MULTIFORME usually caused by an adverse reaction to drugs such as the SULPHONAMIDES. (Albert Mason Stevens, 1884–1935, American paediatrician; and Frank Chambliss Johnson, 1894–1934, American paediatrician).

Stevens-Johnson syndrome

A severe form of erythema multiforme in which the systemic symptoms are severe and the lesions extensive, involving multiple body areas, especially the mucous membranes.Mentioned in: Corticosteroids, Systemic, Kawasaki Syndrome, Toxic Epidermal Necrolysis

Baader,

Ernst, German physician. Baader dermatostomatitis - Synonym(s): Stevens-Johnson syndrome

Johnson,

Frank Chambliss, U.S. pediatrician, 1894-1934. Stevens-Johnson syndrome - see under Stevens, Albert Mason

Stevens,

Albert Mason, U.S. pediatrician, 1884-1945. Stevens-Johnson syndrome - a bullous form of erythema multiforme. Synonym(s): Baader dermatostomatitis; ectodermosis erosiva pluriorificialis; erythema multiforme bullosum; erythema multiforme exudativum; erythema multiforme major

Ste·vens-John·son syn·drome

(stē'vĕnz jon'sŏn sin'drōm) A bullous form of erythema multiforme that may be extensive, involving the mucous membranes and large areas of the body.

单词	stevens-johnson syndrome
释义	Stevens-Johnson syndrome Ste·vens-John·son syndrome S0750750 (stē′vənz-jŏn′sən)n. A severe inflammatory eruption of the skin and mucous membranes, usually occurring after an infection, with malignancy, or as an allergic reaction to drugs or other substances. [After Albert Mason Stevens (1884-1945) and Frank Chambliss Johnson (1894-1934), American pediatricians.] EncyclopediaSeesyndrome Stevens-Johnson syndrome Stevens-Johnson syndrome [ste´venz jon´son] a severe and sometimes fatal form of erythema multiforme in which the lesions may involve the oral and anogenital mucosa, eyes, and viscera, associated with such constitutional symptoms as malaise, headache, fever, arthralgia, and conjunctivitis. Ste·vens-John·son syn·drome (stē'vĕnz jon'sŏn), a bullous form of erythema multiforme that may be extensive, involving the mucous membranes and large areas of the body; it may produce serious subjective symptoms and may have a fatal termination. See also: ocular-mucous membrane syndrome. Synonym(s): erythema multiforme bullosum, erythema multiforme exudativum, erythema multiforme major Ste·vens-John·son syn·drome (stē'vĕnz jon'sŏn), a bullous form of erythema multiforme that may be extensive, involving the mucous membranes and large areas of the body; it may produce serious subjective symptoms and may have a fatal termination. See also: ocular-mucous membrane syndrome. Synonym(s): erythema multiforme bullosum, erythema multiforme exudativum, erythema multiforme major Stevens-Johnson syndrome (stē′vənz-jŏn′sən)n. A severe inflammatory eruption of the skin and mucous membranes, usually occurring after an infection, with malignancy, or as an allergic reaction to drugs or other substances. Stevens-Johnson syndrome Dermatology A variant of erythema multiforme characterized by purpuric macules or atypical targetoid lesions with focal confluence and epithelial detachment covering < 10% of body surface;¹⁄₂ are reactions to drugs–eg, sulfonamides, anticonvulsants, allopurinol, etc; 10-30% are accompanied by systemic Sx Clinical Fever, erosive stomatitis, lesions of anogenital mucosa, conjunctiva–keratitis, corneal erosions, RTIs; < 5% are fatal Treatment Delete offending drug Ste·vens-John·son syn·drome (stē'vĕnz jon'sŏn sin'drōm) A bullous form of erythema multiforme that may be extensive, involving the mucous membranes and large areas of the body; it may produce serious subjective symptoms and may be fatal. Stevens-Johnson syndrome S18-899220 (ste'venz-jon'son) [Albert M. Stevens, 1884–1945, Frank C. Johnson, 1894–1934, U.S. pediatricians] STEVENS-JOHNSON SYNDROMEA systemic skin disease, probably identical to toxic epidermal necrolysis, that produces fevers and lesions of the oral, conjunctival, and vaginal mucous membranes. It is marked by a cutaneous rash that is often widespread and severe. Skin loss may lead to dehydration, infection, or death. See: illustration; erythema multiformeillustration Stevens-Johnson syndrome A rare but severe condition involving skin and MUCOUS MEMBRANES of the eyes, mouth, nose and genitals and featuring ulceration and loss of epithelium with abnormal adhesions. A form of ERYTHEMA MULTIFORME usually caused by an adverse reaction to drugs such as the SULPHONAMIDES. (Albert Mason Stevens, 1884–1935, American paediatrician; and Frank Chambliss Johnson, 1894–1934, American paediatrician). Stevens-Johnson syndrome A severe form of erythema multiforme in which the systemic symptoms are severe and the lesions extensive, involving multiple body areas, especially the mucous membranes.Mentioned in: Corticosteroids, Systemic, Kawasaki Syndrome, Toxic Epidermal Necrolysis Baader, Ernst, German physician. Baader dermatostomatitis - Synonym(s): Stevens-Johnson syndrome Johnson, Frank Chambliss, U.S. pediatrician, 1894-1934. Stevens-Johnson syndrome - see under Stevens, Albert Mason Stevens, Albert Mason, U.S. pediatrician, 1884-1945. Stevens-Johnson syndrome - a bullous form of erythema multiforme. Synonym(s): Baader dermatostomatitis; ectodermosis erosiva pluriorificialis; erythema multiforme bullosum; erythema multiforme exudativum; erythema multiforme major Ste·vens-John·son syn·drome (stē'vĕnz jon'sŏn sin'drōm) A bullous form of erythema multiforme that may be extensive, involving the mucous membranes and large areas of the body.
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Stevens-Johnson syndrome

Ste·vens-John·son syndrome

Stevens-Johnson syndrome

Stevens-Johnson syndrome

Ste·vens-John·son syn·drome

Ste·vens-John·son syn·drome

Stevens-Johnson syndrome

Stevens-Johnson syndrome

Ste·vens-John·son syn·drome

Stevens-Johnson syndrome

Stevens-Johnson syndrome

Stevens-Johnson syndrome

Baader,

Johnson,

Stevens,

Ste·vens-John·son syn·drome