extrathoracic sarcoidosis - ترجمة إلى العربية
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extrathoracic sarcoidosis - ترجمة إلى العربية

DISEASE CHARACTERIZED BY THE GROWTH OF COLLECTIONS OF INFLAMMATORY CELLS (GRANULOMAS) IN MULTIPLE ORGANS
Besnier-Boeck-Schaumann disease; Sarcoidoisis; Sarchoidosis; Sarcoidosis, pulmonary; Besnier-Boeck disease; Besnier Boeck disease; Boeck's Sarcoid; Boeck-Schaumann disease; Hutchinson-Boeck disease; Sarcoiditis; Sarcoydosis; Systemic sarcoidosis; Pulmonary sarcoidosis; Boeck's sarcoid; Box sarcoid; Tache de bougie; Scar sarcoidosis; Sarcoid granuloma; Sarcoidosis in scar; Acute with erythema nodosum sarcoidosis; Plaque sarcoidosis; Subcutaneous nodular sarcoidosis; Maculopapular sarcoidosis; Nodular sarcoidosis; Papular sarcoidosis; Cutaneous sarcoidosis; Besnier Boeck Schaumann disease; Sarcoïdosis; Early-onset sarcoidosis; Besnier–Boeck–Schaumann disease; Cardiac sarcoidosis; Causes of sarcoidosis
  • Gross pathology image showing sarcoidosis with honeycombing: Prominent honeycombing is present in the lower lobes accompanied by fibrosis and some honeycombing in the upper lungs. Honeycombing consists of cystically dilated airways separated by scar tissue resembling the honeycomb of bees. It is a nonspecific end stage of many types of interstitial lung disease.
  • archive-date=May 7, 2009 }}</ref>

extrathoracic sarcoidosis      
‎ ساركويدٌ خارِجَ الصَّدْر‎
Besnier Boeck disease         
‎ داءُ بينييه بِيك,السَّارْكُويد‎
sarcoidosis         
‎ ساركويد‎

تعريف

sarcoidosis
[?s?:k??'d??s?s]
¦ noun Medicine a chronic disease in which the lymph nodes become enlarged and granulomas appear in the reticuloendothelial system.

ويكيبيديا

Sarcoidosis

Sarcoidosis (also known as Besnier-Boeck-Schaumann disease) is a disease involving abnormal collections of inflammatory cells that form lumps known as granulomata. The disease usually begins in the lungs, skin, or lymph nodes. Less commonly affected are the eyes, liver, heart, and brain, though any organ can be affected. The signs and symptoms depend on the organ involved. Often, no, or only mild, symptoms are seen. When it affects the lungs, wheezing, coughing, shortness of breath, or chest pain may occur. Some may have Löfgren syndrome with fever, large lymph nodes, arthritis, and a rash known as erythema nodosum.

The cause of sarcoidosis is unknown. Some believe it may be due to an immune reaction to a trigger such as an infection or chemicals in those who are genetically predisposed. Those with affected family members are at greater risk. Diagnosis is partly based on signs and symptoms, which may be supported by biopsy. Findings that make it likely include large lymph nodes at the root of the lung on both sides, high blood calcium with a normal parathyroid hormone level, or elevated levels of angiotensin-converting enzyme in the blood. The diagnosis should only be made after excluding other possible causes of similar symptoms such as tuberculosis.

Sarcoidosis may resolve without any treatment within a few years. However, some people may have long-term or severe disease. Some symptoms may be improved with the use of anti-inflammatory drugs such as ibuprofen. In cases where the condition causes significant health problems, steroids such as prednisone are indicated. Medications such as methotrexate, chloroquine, or azathioprine may occasionally be used in an effort to decrease the side effects of steroids. The risk of death is 1–7%. The chance of the disease returning in someone who has had it previously is less than 5%.

In 2015, pulmonary sarcoidosis and interstitial lung disease affected 1.9 million people globally and they resulted in 122,000 deaths. It is most common in Scandinavians, but occurs in all parts of the world. In the United States, risk is greater among black people as opposed to white people. It usually begins between the ages of 20 and 50. It occurs more often in women than men. Sarcoidosis was first described in 1877 by the English doctor Jonathan Hutchinson as a non-painful skin disease.