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1.
SQUMJ-Sultan Qaboos University Medical Journal. 2006; 6 (1): 41-45
Dans Anglais | IMEMR | ID: emr-81175

Résumé

To 1. Highlight the demographic characteristics, clinical features, laboratory investigations and outcome if possible of a relatively rare disease [Adult Onset Still's Disease [AOSD]] and 2. To compare our results with those reported earlier by others. A retrospective review of the clinical, laboratory and radiological manifestations in 6 patients admitted with AOSD. Data were collected from clinical summary of each case highlighting the demographic, clinical features and relevant investigation. The diagnosis was made on clinical base and supported by the laboratory and radiological examinations to confirm the diagnosis and/or exclude other differential diagnoses. Mean age of patients [21.6], presence of fever [80.2%] and its pattern, skin rash [80.2%], arthralgia[100%], arthritis[66.65%], and the duration of morning stiffness, all these findings were compatible with earlier results. However young adult females constitute [80.2%] of our small group, which is quite high in comparison with others. Splenomegaly [33.3%], hepatomegaly[16.6%], and lymphadenopathy[16.6%] were less than that reported by others who have more serious intra-abdominal visceral involvement. One patient [16.65%] had a fatal pulmonary embolism, although usually pulmonary involvement is a mild one. None of our patients had neurological, ophthalmological or hearing involvement. The results of the investigations and radiological findings are more or less similar to those in other series. The clinical and laboratory characteristics of our small number of patients are more or less consistent with findings of others. It is important to keep in mind that AOSD is an uncommon syndrome with a range of signs and symptoms which are non-specific and may simulate a variety of connective tissue and general medical problems. Differences in the expression of AOSD were found between patients from different locations and the disease can be responsible for life-threatening complications


Sujets)
Adulte , Femelle , Humains , Mâle , Maladie de Still débutant à l'âge adulte/physiopathologie , Études rétrospectives , Arthrite juvénile , Fièvre d'origine inconnue , Antirhumatismaux
2.
Journal of the Faculty of Medicine-Baghdad. 1997; 39 (1): 131-6
Dans Anglais | IMEMR | ID: emr-45038

Résumé

To asses the relation between Abdominal wall hernia and joint hypermobility. [100] Patients with abdominal wall hernia were examined for joint hypermobility and compared with an age and sex matched control group without abdominal wall hernia. Mobility was measured on a scale of 0-9. The abdominal wall hernia group had more patients who were hypermobile [P=<0.01] and their total mobility score were higher than the control group [P=<0.001]. Joint complaints were similar in both groups while the Prevalence of backache in abdomined wall hernia group was one and a half the control group


Sujets)
Humains , Mâle , Femelle , Hernie , Instabilité articulaire , Hernie crurale , Hernie inguinale , Prévalence
3.
Journal of the Faculty of Medicine-Baghdad. 1995; 37 (4): 507-512
Dans Anglais | IMEMR | ID: emr-37782

Résumé

Forty one patients with different rheumatological diseases were involved in this retrospective study to assess the toxic side effects of gold compounds. More than half of the patients [56%] developed one or more such effects. The most common was cutaneous rash [36%] mainly Eczematous, Psoriatic, Lichenoid, and Pityriasis Rosea like rash. The renal affection followed cutaneous [12.5%], and lastly the haematological side effects [6.6%]. Withdrawal of chrysotherapy resulted in disappearance of the rash within weeks. Less common side effects were transient fainting attacks and glossitis which developed during the course of treatment, usually these were mild and did not necessitate withdrawal of therapy


Sujets)
Humains , Mâle , Femelle , Rhumatismes/thérapie , Antirhumatismaux/effets indésirables
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