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Sarcoidosis

From Wikipedia
sarcoidosis
designated intractable/rare disease, class of disease
Subclass oftype IV hypersensitivity, disease Edit
Dem name afterErnest Besnier Edit
Health specialtyhematology, dermatology, pulmonology, ophthalmology Edit
Symptoms and signscough, dyspnea Edit
Possible treatmentibuprofen, methotrexate Edit
Genetic associationBTNL2 Edit
External data available at URLhttp://www.nanbyou.or.jp/entry/110 Edit
ICD-9-CM135 Edit
NCI Thesaurus IDC34995 Edit

Sarcoidosis, dem sanso know as Besnier–Boeck–Schaumann disease, be a non-infectious granulomatous disease wey dey involve abnormal collections of inflammatory cells wey dey form lump dem know as granulomata.[1] De disease usually dey begin insyd de lungs, skin, anaa lymph nodes.[1] Less commonly affected be de eyes, liver, heart, den brain, though any organ fi be affected.[1] De signs den symptoms dey depend on de organ involved.[1] Often, no symptoms anaa mild symptoms per be seen.[1] Wen e affect de lungs, wheezing, coughing, shortness of breath, anaa chest pain fi occur.[2] Sam fi get Löfgren syndrome, plus fever, enlarged hilar lymph nodes, arthritis, den a rash dem know as erythema nodosum.[1]

De cause of sarcoidosis be unknown.[1] Sam believe e fi be secof an immune reaction to a trigger such as an infection anaa chemicals insyd those wey be genetically predisposed.[3][4] Those plus affected family members be at greater risk.[5] Diagnosis partly be based on signs den symptoms, wich fi be supported by biopsy.[6] Findings wey dey make am likely dey include large lymph nodes at de root of de lung on both sides, high blood calcium plus a normal parathyroid hormone level, anaa elevated levels of angiotensin-converting enzyme insyd de blood.[6] Dem for make de diagnosis only after dem exclude oda possible causes of similar symptoms such as tuberculosis.[6]

Sarcoidosis fi resolve widout any treatment within a few years.[1][7] However, sam people fi get long-term anaa severe disease.[7] Sam symptoms fi be improved plus de use of anti-inflammatory drugs such as ibuprofen.[8] Insyd cases wer de condition dey cause significant health problems, steroids such as prednisone be indicated.[9] Medications such as methotrexate, chloroquine, anaa azathioprine occasionally fi be used in an effort to decrease de side effects of steroids.[9] De risk of death be 1–7%.[7] De chance of de disease returning insyd sam bro wey na dem previously get am be less dan 5%.[1]

Insyd 2015, na pulmonary sarcoidosis den interstitial lung disease affect 1.9 million people globally wey na e result in 122,000 deaths.[10][11] E be most common insyd Scandinavians, buh dey occur insyd all parts of de world.[12] Insyd de United States, risk be greater among black dan white people.[12] E usually dey begin between de ages of 20 den 50.[5] E dey occur more often insyd women dan men.[5] Na de English doctor Jonathan Hutchinson first describe sarcoidosis insyd 1877 as a non-painful skin disease.[13]

References

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  1. 1 2 3 4 5 6 7 8 9 "What Is Sarcoidosis?". NHLBI. June 14, 2013. Archived from the original on 6 April 2016. Retrieved 28 March 2016.
  2. "What Are the Signs and Symptoms of Sarcoidosis?". NHLBI. June 14, 2013. Archived from the original on 7 April 2016. Retrieved 29 March 2016.
  3. Baughman RP, Culver DA, Judson MA (March 2011). "A concise review of pulmonary sarcoidosis". American Journal of Respiratory and Critical Care Medicine. 183 (5): 573–81. doi:10.1164/rccm.201006-0865CI. PMC 3081278. PMID 21037016.
  4. "What Causes Sarcoidosis?". NHLBI. June 14, 2013. Archived from the original on 6 April 2016. Retrieved 28 March 2016.
  5. 1 2 3 "Who Is at Risk for Sarcoidosis?". NHLBI. June 14, 2013. Archived from the original on 7 April 2016. Retrieved 28 March 2016.
  6. 1 2 3 Govender P, Berman JS (December 2015). "The Diagnosis of Sarcoidosis". Clinics in Chest Medicine. 36 (4): 585–602. doi:10.1016/j.ccm.2015.08.003. PMID 26593135.
  7. 1 2 3 Wijsenbeek MS, Culver DA (December 2015). "Treatment of Sarcoidosis". Clinics in Chest Medicine. 36 (4): 751–67. doi:10.1016/j.ccm.2015.08.015. PMID 26593147.
  8. Drent M, Cremers JP, Jansen TL (May 2014). "Pulmonology meets rheumatology in sarcoidosis: a review on the therapeutic approach". Current Opinion in Rheumatology. 26 (3): 276–84. doi:10.1097/bor.0000000000000052. PMID 24614277. S2CID 24353355.
  9. 1 2 Judson MA (February 2016). "Corticosteroids in Sarcoidosis". Rheumatic Disease Clinics of North America. 42 (1): 119–35, ix. doi:10.1016/j.rdc.2015.08.012. PMID 26611555.
  10. Vos, Theo; et al. (October 2016). "Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1545–1602. doi:10.1016/S0140-6736(16)31678-6. PMC 5055577. PMID 27733282.
  11. Wang, Haidong; et al. (October 2016). "Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980–2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1459–1544. doi:10.1016/S0140-6736(16)31012-1. PMC 5388903. PMID 27733281.
  12. 1 2 Kobak S (October 2015). "Sarcoidosis: a rheumatologist's perspective". Therapeutic Advances in Musculoskeletal Disease. 7 (5): 196–205. doi:10.1177/1759720x15591310. PMC 4572362. PMID 26425148.
  13. James DG, Sharma OP (September 2002). "From Hutchinson to now: a historical glimpse" (PDF). Current Opinion in Pulmonary Medicine. 8 (5): 416–23. doi:10.1097/00063198-200209000-00013. PMID 12172446. Archived (PDF) from the original on 2016-03-04.
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