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2.
Eur J Intern Med ; 16(8): 545-50, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16314234

ABSTRACT

In this review we summarize a number of cases of Sweet's syndrome (SS) associated with sarcoidosis that have been reported in the English literature. In all of the cases, the two disorders were diagnosed simultaneously. Patients with both disorders were younger and had a higher rate of fever than patients with SS alone. In this group of patients, we found a trend toward less skin involvement of the face and trunk, more involvement of the upper limbs, and more atypical skin lesions, particularly papules. The association of the two disorders seems to be more related to a subset of acute sarcoidosis (Lofgren's syndrome). All of the patients in this group had a benign course and self-limiting disease. Thus, SS in association with sarcoidosis could be considered a favorable prognostic factor. Although SS has a high rate of recurrence, no recurrence occurred in this group of patients during follow-up.

10.
Isr Med Assoc J ; 2(6): 433-7, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10897233

ABSTRACT

BACKGROUND: Acute rheumatic fever is considered a relatively uncommon disease in developed countries. Although cases are encountered in the Nazareth area in Israel, no systematic study of this disease has been done in the last 20 years. OBJECTIVE: To study the incidence and characteristics of acute rheumatic fever cases in the Nazareth area during the last decade. METHODS: Cases of acute rheumatic fever diagnosed according to the modified Jones criteria were identified in two hospitals in the Nazareth area during the 10 years. These two hospitals receive about 75% of non-obstetric referrals to the emergency room. Clinical, laboratory and treatment data of these patients were documented and the incidence of disease calculated. The population census in the Nazareth area was obtained from the Central Bureau of Statistics. RESULTS: Forty-four patients, with a mean age of 18 years, were identified. The mean annual incidence was 5 cases/100,000 population. Arthritis was found in 98% of the patients (migratory in 52%) and carditis in 34%, but only one patient had a subcutaneous nodule, and none had either erythema marginatum or chorea. Only one patient with carditis developed heart failure a few months later due to severe mitral stenosis. CONCLUSION: Rheumatic fever in the Nazareth area is still manifest. The mean age of the patients was higher than found previously. In only half of the patients was the arthritis migratory, with other major manifestations of rheumatic fever found only rarely.


Subject(s)
Rheumatic Fever/epidemiology , Acute Disease , Adolescent , Adult , Arthritis, Rheumatoid/complications , Child , Child, Preschool , Female , Humans , Israel/epidemiology , Male , Myocarditis/complications
11.
Lupus ; 4(1): 19-22, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7539322

ABSTRACT

A patient with hyperglobulinemic purpura of Waldenstrom and systemic lupus erythematosus is reported. The coexistence of these two conditions which share a number of common clinical and laboratory features is rare. Treatment of the patient with prednisone, colchicine and hydroxychloroquine led to the improvement of the cutaneous vasculitis and a drop in ESR, serum gamma globulins and IgM and IgG rheumatoid factors. The features of nine other cases and the immunopathogenesis of the disease are reviewed.


Subject(s)
Lupus Erythematosus, Systemic/complications , Waldenstrom Macroglobulinemia/complications , Adult , Colchicine/therapeutic use , Female , Humans , Hydroxychloroquine/therapeutic use , Immunoglobulin G/blood , Immunoglobulin M/blood , Lupus Erythematosus, Systemic/blood , Lupus Erythematosus, Systemic/drug therapy , Prednisone/therapeutic use , Rheumatoid Factor/blood , Skin/blood supply , Vasculitis/therapy , Waldenstrom Macroglobulinemia/blood , Waldenstrom Macroglobulinemia/drug therapy , gamma-Globulins/metabolism
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