Severe CD8 Deficiency in a Child with Miliary Tuberculosis
نویسندگان
چکیده
منابع مشابه
Recurrent Venous Thromboembolic Events in a Child with Severe Factor X Deficiency
Congenital factor X deficiency is a rare autosomal recessive bleeding disorder that presents with variable bleeding tendency and prolonged coagulation tests, prothrombin time, and partial thromboplastin time. Thromboembolic events have not been reported in patients with factor X deficiency yet. Herein, we report a patient with factor X deficiency who had recurrent venous thromboembolic events.
متن کاملMiliary Tuberculosis
این مقاله موردی از سل ارزنی را گزارش کرده که پس از بروز سل و ۲ ماه شیمی درمانی، با ضایعات پوستی، استئومیلیت انگشتان و التهاب پیشرونده و غیر معمول رباطها عارض گردیده است.
متن کاملMiliary tuberculosis in adults.
Of 40 adults with miliary tuberculosis 24 had "overt" disease; in them miliary mottling was usually present on the chest radiograph, and tubercle bacilli were readily isolated from sputum, urine, or cerebrospinal fluid. In the remaining 16 patients the disease was termed "cryptic" because its usual clinical and radiographic features were absent. This cryptic type is as common as the overt type ...
متن کاملMiliary tuberculosis presenting with thyrotoxicosis.
A male patient is described who presented with thyrotoxicosis, and a large painful neck mass. From the excised mass and stomach aspiration Mycobacterium tuberculosis was cultured and a diagnosis of miliary tuberculosis was made. The thyrotoxicosis was attributed to tuberculous thyroiditis.
متن کاملMiliary tuberculosis
The aim of this study was to determine the clinical features, and outcome of the patients with miliary tuberculosis (TB).We retrospectively evaluated 263 patients (142 male, 121 female, mean age: 44 years, range: 16-89 years) with miliary TB. Criteria for the diagnosis of miliary TB were at least one of the followings in the presence of clinical presentation suggestive of miliary TB such as pro...
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ژورنال
عنوان ژورنال: Journal of Tropical Pediatrics
سال: 2005
ISSN: 1465-3664,0142-6338
DOI: 10.1093/tropej/fmi053