I-pulmonary fibrosis iyinqamuzana yamaphaphu angase abe ngenxa yezimbangela eziningi. Ihlukaniswe njengengxenye yeqembu lezifo zamaphaphu eyaziwa njenge-interstitial lung disease. Abantu abane-fibrosis ye-pulmonary bavame ukuphefumula okuqhubekayo. Ukwelashwa nokuchazwa kwe-pulmonary fibrosis kungahluka kuye ngokuthi imbangela, kodwa ngokuvamile, ayikho ikhambi le-fibrosis ye-pulmonary.
Ngesilinganiso esincane, izindonga ze- alveoli (ama-sac ezincane ezinomoya emaphashini) ziyabonakala. Lokhu kuvimbela i-alveoli ukuba ikhulise futhi ivumelane kahle ngesikhathi sokuphefumula.
Izimbangela
Kunezimbangela eziningi ze-fibrosis ye-pulmonary, ezinye zazo zihlanganisa:
- Idiopathic pulmonary fibrosis - Yilapho kungekho mbuzo oqondile ongatholakala nge-fibrosis emaphashini. Ngaphezu kokubangela izimpawu zodwa, i-IPF iyinhloko engozini yokuthuthukisa umdlavuza wamaphaphu.
- Izifo, ikakhulukazi izifo ezithathelwanayo.
- Ukuveza izinto ezinobuthi (njenge-asbestos ne-silika uthuli).
- Amagciwane .
- Eminye imithi efana ne-chemotherapy yezidakamizwa ze-Cytoxan, kanye nesifo sokutheleleka kwesibindi Macrodantin (nitrofurantoin).
- Ama-pneumoconioses njenge-black lung disease.
- Ukwelashwa kwezidakamizwa esifubeni somdlavuza wamaphaphu, umdlavuza webele, noma i-lymphomas. I-fibrosis yama-lung ivame ukuqala nge- radiation pneumonitis nokuvuvukala kwamapayipi ngenxa yokwelashwa kwemisebe. Uma i-radiation pneumonitis ingatholakali, noma uma ingaphatheki kahle, i-radiation permanent fibrosis ingaba umphumela. Abacwaningi babheka izindlela zokusiza ukuvimbela lo mphumela ohlangothini lwe-radiation therapy yomdlavuza. I-pulmonary fibrosis ingase ikhule izinyanga kuze kube yiminyaka emva kokuba imithi yokwelapha igcwaliswe.
- I-Genetics. Kubonakala sengathi ngezinye izikhathi i-fibrosis ye-pulmonary igijima emindenini ephakamisa isici sezofuzo.
- Isifo se-reflux esisemathunjini (GERD) . I-reflux ye-longness ye-longue ingaba yingozi engozini ye-lung fibrosis.
Izimpawu
Izimpawu ze-fibrosis ye-pulmonary zingabandakanya:
- Ukuphefumula, ngokuvamile ukuqala kokuzivocavoca bese uqhubeka kuze kube yilapho umuntu engapheli ukuphefumula ekuphumuleni. Lona uphawu oluvame kakhulu lwe-fibrosis ye-pulmonary.
- Ukukhwehlela owomile.
- Ubuhlungu besifuba.
- Amapulpitations.
- Ukulahlekelwa kwesisindo.
- Ukukhathala.
- Ama-muscle nama-joint aches.
- I-Clubbing - Lesi simo lapho ukuphela kweminwe kubheka khona i-spoon ephikisiwe.
Ukuxilongwa
Ukuxilongwa kwe-pulmonary fibrosis kungabandakanya ukuhlanganiswa kwezivivinyo ezingezansi, kanye nokuhlolwa ukukhipha ezinye zezimbangela zesifo.
- I-x-ray yekhanda kanye / noma isifuba CT scan.
- Ukuhlolwa kokusebenza kwamapulmonary .
- Ukuhlola igazi kwegazi.
- I-liop biopsy.
Ukwelapha
Ukwelashwa kwe-pulmonary fibrosis kuzoxhomeka ekubambeni. Muva nje, ukwelashwa sekutholakale ikakhulukazi kubantu abane-fibrosis ye-idiopathic pulmonary .
Njengoba i-fibrosis ye-pulmonary inencazelo ehlala njalo, ukwelashwa kuhloswe ukuvimbela ukuwohloka kwesifo nokusiza abantu ukuba babhekane nezinkinga zesifo. Imithi ingasiza ekuvimbeleni ukuqhuma okuqhubekayo, nokuvuselelwa kwe-pulmonary , imithi, kanye nokwelapha oksijini uma kunzima kakhulu ukusiza abantu ukuba baphile impilo esebenzayo naphezu kokuhlushwa yi-fibrosis ye-pulmonary. Kwabanye abantu, ukufakelwa kwamaphaphu kuyindlela engenzeka, futhi njengamanje, i-fibrosis yamaphaphu iyisizathu esiholela phambili sokuguqula amaphaphu e-United States.
Izinkinga
Njengoba amaphaphu eqala ukusibeka kancane, ungase ucabange ukuthi kunzima kakhulu igazi ukuba udlule emaphashini okuzoholela ekucindezeni kwegazi okuphezulu kulezi mithini yegazi, futhi ingxenye yenhliziyo isebenza ukudlulisa igazi emaphashini kufanele sisebenze kanzima.
Ezinye izinkinga zingabandakanya:
- Umfutho wegazi ophezulu wegazi - Ukwanda kwengcindezi yegazi emithonjeni yegazi yamapulmonary
- I-Cor pulmonale - Ukuhluleka kwenhliziyo okubandakanya ohlangothini lwesokudla senhliziyo (iningi lokuhluleka kwenhliziyo kusho ukuhluleka kwenhliziyo kwesokunxele, ngenhliziyo inenkinga yokupompa igazi kuwo wonke umzimba.)
- Isifo senhliziyo.
- Umdlavuza we-Lung - I-Pulmonary fibrosis ihlotshaniswa nengozi eyengeziwe yokwenza umdlavuza wamaphaphu.
- Ama-blood clots emilenzeni engakwazi ukuya emaphashini (emaphasini we-pulmonary emboli.)
Isibikezelo
Ukuchazwa kwe-pulmonary fibrosis futhi kuncike ekubambeni okubangela. Ngokuvamile, isikhathi sokuphila komuntu onomfutho we-pulmonary fibrosis sivela emkhatsini weminyaka engu-3 no-5, kodwa lokhu kungahluka kakhulu ngezimbangela ezihlukahlukene naphakathi kwabantu abahlukene.
Imithombo:
I-American Lung Association. I-Pulmonary Fibrosis.
Ilabhulali Kazwelonke Yezokwelapha. I-MedlinePlus. I-Pulmonary Fibrosis. Kubuyekezwe 07/13/16.