A STONE MINER WITH SILICOSIS- CASE REPORT

نویسندگان
چکیده

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A stone miner with both silicosis and constrictive pericarditis: case report and review of the literature

BACKGROUND The working environment of stone miners has been believed to cause their susceptibility to respiratory diseases. Silicosis is an occupational disease caused by exposure to crystalline silica dust which is marked by inflammation and scarring in the lung. The immune system boosted after the silica invasion led to self-damage and lay the foundation of silicosis pathogenesis. Silicosis c...

متن کامل

Ureteral stone presenting as acute prostatitis: A case report of a COVID-19 patient with distal ureteral stone

1. Fellowship of Endouorology, Professor, Urology and Nephrology Research Center, Hamadan University of Medical Sciences, Hamadan, Iran 2.Resident of Urology, Urology and Nephrology Research Center, Hamadan University of Medical Sciences, Hamadan, Iran. 3. Resident of Urology, , School of Medicine , Isfahan University of Medical Sciences, Isfahan, Iran Abstract Distal ureterolithiasis is on...

متن کامل

Sjögren’s Syndrome and Silicosis – a Case Report

Sjögren's syndrome is an autoimmune disease of unknown etiology where immune response to self-antigens is believed to result from interactions between genetic and environmental factors. We describe the case of a patient who has been diagnosed with Sjögren's syndrome based on typical clinical and immunological parameters. The clinical picture was dominated by the respiratory symptoms, and radiog...

متن کامل

Retroperitoneal silicosis mimicking pancreatic carcinoma in an Alpine miner with chronic lung silicosis.

A miner, known to have had lung silicosis for 30 years, was investigated for abdominal pain. A retroperitoneal mass was found, in which histological examination showed an inflammatory reaction to silica.

متن کامل

Stone Man: A Case Report

Fibrodysplasia ossificans progressiva (FOP) is a rare hereditary connective tissue disease characterized by the progressive ectopic ossification of ligaments, tendons, and facial and skeletal muscles throughout life. Symptoms begin in childhood as localized soft tissue swellings. Immobility and articular dysfunction appear with involvement of the spine and proximal extremities. The temporomandi...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Journal of Evidence Based Medicine and Healthcare

سال: 2018

ISSN: 2349-2562,2349-2570

DOI: 10.18410/jebmh/2018/20