Results 231 to 240 of about 72,111 (278)

Mucocutaneous Lymph Node Syndrome

Journal of Computer Assisted Tomography, 1984
A 3-year-old child presented with a short clinical history of fever and diffuse cervical lymphadenopathy, and the diagnosis of mucocutaneous lymph node syndrome was reached. We include a discussion of the case history and a brief review of this disorder.
Michael Fine, James Stankiewicz, Cesar E. Menendez, Mark S. Puczynski   +3 more
openaire   +3 more sources

Morphological observations on the vasculitis in the mucocutaneous lymph node syndrome

European Journal of Pediatrics, 1978
Sachiko Hirose, Yoshihiro Hamashima
openalex   +2 more sources

Sonography in the diagnosis and management of hydrops of the gallbladder in children with mucocutaneous lymph node syndrome.

Pediatrics, 1980
Acute hydrops of the gallbladder is described in four patients who had mucocutaneous lymph node syndrome. Diagnosis was readily made with gray-scale ultrasound, and the patients were followed with this technique.
T. Slovis, D. Hight, A. Philippart, R. Dubois   +3 more
semanticscholar   +1 more source

Are infantile periarteritis nodosa with coronary artery involvement and fatal mucocutaneous lymph node syndrome the same? Comparison of 20 patients from North America with patients from Hawaii and Japan.

Pediatrics, 1977
We reviewed available clinical and pathologic autopsy material from 20 patients with infantile periarteritis nodosa with coronary artery involvement (IPN) from the continental United States, two Hawaiian patients with fatal mucocutaneous lymph node ...
B. Landing, E. Larson
semanticscholar   +1 more source

Ultrasonography of mucocutaneous lymph node syndrome.

Radiology, 1981
Clinical findings associate mucocutaneous lymph node syndrome (MCLS) with diffuse arteritis leading to the formation of large aneurysms. Ultrasound assists in the diagnosis of the associated aneurysms, and aids the clinical management of the patients.
H Kangarloo, Josephine Isabel-Jones, M S Vangrov, H Heins, T G Di Sessa   +4 more
openaire   +3 more sources

Mucocutaneous lymph node syndrome (MLNS): a disease widespread in Japan which demands our attention.

Pediatrics, 1974
In 1967 Kawasaki of Tokyo1 described 50 cases of a seemingly self-limited disease syndrome of infants and young children, which he designated as mucocutaneous lymph node syndrome (MLNS). The patients ranged in age from 2 months to 9 years, more than half
G. Fetterman, Y. Hashida
semanticscholar   +1 more source

Mucocutaneous lymph node syndrome with necrotic pharyngitis

European Journal of Pediatrics, 1980
We report a case of Kawasaki disease in which some unusual symptoms, including petechiae, an urticaria-like eruption, and necrotic pharyngitis, made the diagnosis difficult. No complications were detected during a follow-up period of 15 months.
Brion, Luc, Bachelart, D., Szliwowski, Henri, Dickstein, M, Tondeur, Marianne, Heenen, Michel, Courtoy, Michel   +6 more
openaire   +3 more sources

HLA antigens in mucocutaneous lymph node syndrome in New England.

Pediatrics, 1981
HLA antigens were evaluated in 27 patients with mucocutaneous lymph node syndrome (Kawasaki disease) in the Boston area. In contrast to previous Japanese studies, no increase of HLA-Bw22 was found.
Alan M. Krensky, William Berenberg, K. Shanley, Edmond J. Yunis   +3 more
semanticscholar   +1 more source

Mucocutaneous Lymph Node Syndrome in Adults

JAMA: The Journal of the American Medical Association, 1980
To the Editor.— The letters between James K. Todd, MD, and E. Dale Everett, MD (243:1631, 1980), concerning the question of whether mucocutaneous lymph node syndrome (MLNS) (Kawasaki disease) can occur in adults are of interest to us as authors of a report on this syndrome in an adult (discussed with Dr Kawasaki in 1976 before submission of our report
Harry M. Bauer, Virginia A. Anderson
openaire   +2 more sources

Ocular manifestations of Kawasaki disease (mucocutaneous lymph node syndrome).

Canadian Journal of Ophthalmology-journal Canadien D Ophtalmologie, 1982
This paper describes nine patients, five girls and four boys aged 4 months to 7 years (mean 3 3/4 years), who had the clinical and laboratory features of Kawasaki disease (mucocutaneous lymph node syndrome).
J. Jacob, R. Polomeno, Z. Chad, N. Lapointe   +3 more
semanticscholar   +1 more source