I-pulmonary fibrosis yinkqutyana yemiphunga engenzeka ngenxa yezizathu ezininzi. Ikwahlulo njengenxalenye yeqela leempawu zeemiphunga ezibizwa ngokuba yi-interstitial disease disease. Abantu abane-pulmonary fibrosis banokuphefumula okufutshane. Unyango kunye nokugxekwa kwe-pulmonary fibrosis kuyahlukahluka kuxhomekeke kweso sizathu, kodwa ngokubanzi, akukho naluphi unyango lwe-pulmonary fibrosis.
Kwinqanaba elincinci, iindonga ze- alveoli (iimbotyi ezincinci zomoya emaphafini) ziba nzima. Oku kuvimbela i-alveoli ukuba ikhulise kwaye ithengwe kakuhle ngexesha lokuphefumla.
Izizathu
Zininzi ezibangela i-pulmonary fibrosis, ezinye zezi ziquka:
- Idiopathic pulmonary fibrosis - Yilapho kungekho sizathu esicacileyo esinokufumaneka kwi-fibrosis kwimiphunga. Ukongeza ngaphezu kokubangela iimpawu zodwa, i-IPF ingumngcipheko wokuphucula umdlavuza wamaphaphu.
- Izifo, ikakhulukazi izifo zentsholongwane.
- Ukubonakaliswa kwizinto ezinobuthi (ezifana ne-asbestos kunye ne-silika uthuli).
- Utywala .
- Amanye amachiza afana ne-chemotherapy drug Cytoxan, kunye nesichengululo se-macrodantin (nitrofurantoin).
- Iipneumoconioses ezifana nesifo somnyama wamaphaphu.
- Ukunyanga kwamayeza emfubeni kumdlavuza wamaphaphu, umdlavuza webele, okanye i-lymphomas. I-fung fibrosis ivame ukuqala nge- radiation pneumonitis kunye nokuvuvukala kwemiphunga ngenxa yonyango lwe-radiation. Ukuba i-radiation pneumonitis ayifumaneki, okanye ukuba ingaphathwa kakubi, i-radiosis engapheliyo i-fibrosis ingaba ngumphumo. Abaphandi bajonga iindlela zokunceda ukukhusela le mpahla yecandelo lophulo lwe-radiation ngomhlaza. I-pulmonary fibrosis inokuphuhlisa inyanga ukuya kwiminyaka emva kokuba unyango lwemiyeza lugqityiwe.
- Genetics. Kubonakala ukuba ngamanye amaxesha i-pulmonary fibrosis isebenza kwiintsapho ezibonisa i-genetic element.
- Isifo se-reflux esiswini (GERD) . I-acid ye-long reflux ingaba ngumngcipheko we-lung fibrosis.
Iimpawu
Iimpawu ze-pulmonary fibrosis zingaquka:
- Ukuphefumula okuqhelekileyo, ngokuqhelekileyo kuqala ngokuzilolonga kwaye uqhube phambili de kubekho umntu ophefumulayo. Eli liphawu oluqhelekileyo lwe-pulmonary fibrosis.
- Umkhuhlane omile.
- Iintlungu zesifuba.
- Iipilpitations.
- Ukuhla ukusinda.
- Ukukhathala.
- Iimpawu zeMiscle kunye kunye.
- I-Clubbing - Lo mqathango apho ukuphela kweminwe kuthatha ukubonakala kwipuni.
Ukuxilongwa
Ukuxilongwa kwe-pulmonary fibrosis kunokubandakanya ukudibanisa iimvavanyo ezingezantsi, kwakunye neemvavanyo ukulawula ezinye zezizathu zesifo.
- I-x-ray yesifuba kunye / okanye isifuba se-CT.
- ImiSebenzi yovavanyo .
- Uvavanyo lwegazi.
- I-biopsy yomlenze.
Unyango
Unyango lwe-pulmonary fibrosis luya kuxhomekeka kwisizathu. Kungekudala, unyango luye lwafumaneka ngokukodwa kubantu abane-fibrose idiopathic pulmonary fibrosis .
Ekubeni i-pulmonary fibrosis ingcaciso ngokusisigxina, unyango lujoliswe ekukhuseleni ukwanda kwesifo nokunceda abantu bajamelane neempawu zesifo. Amachiza anokunceda ukukhusela ukuvutha komzimba, kunye nokuvuselelwa kwamapulmoni , unyango kunye ne-oksijithi xa kunzima ukunceda abantu baqhube ubomi obunobungozi nangona bephethwe yi-fibrosis ye-pulmonary. Kwabanye abantu, ukutshintshwa kwemiphunga kukukhetha, kwaye okwangoku, i-pulmonary fibrosis yeso sizathu esibangeleyo sokuhamba kwemiphunga e-United States.
Iingxaki
Ekubeni imiphunga iyancipha, unokucinga ukuba kunzima kakhulu igazi ukuba udlule emiphakeni leyo leyo ingakhokelela ekubeni uxinzelelo lwegazi luphezulu kule mijelo yegazi, kunye nenxalenye yentliziyo esebenzayo ukudlula igazi kwimiphunga kufuneka usebenze nzima.
Ezinye iingxaki zingabandakanya:
- I- blood pressure ye-pulmonary - Ukunyuka kwengcinezelo yegazi kwimithambo yegazi ye-pulmonary
- I-Cor pulmonale - Ukungaphumeleli kwintliziyo echaphazelekayo kwintliziyo (ininzi yexesha ukungaphumeleli kwentliziyo kuthetha ukungaphumeleli kwentliziyo yesinxele, kunye nentliziyo inobunzima ukupompa igazi kuwo wonke umzimba.)
- Isifo sentliziyo.
- Umhlaza womlenze - I-Pulmonary fibrosis idibene nomngcipheko okhulayo wokuba nomdlavuza wamaphaphu.
- Igazi livale emilenzeni ekwazi ukuhamba emiphakeni (imitha ye-pulmonary emboli.)
Prognosis
Ukugxekwa kwe-pulmonary fibrosis kuya kuxhomekeka kwimeko ethile. Ngokuqhelekileyo, ukulinda komntu umntu ophethe i-pulmonary fibrosis iphakathi kweminyaka emi-3 neye-5, kodwa oku kungahluka ngokubanzi kwizizathu ezahlukeneyo kunye phakathi kwabantu abahlukeneyo.
Imithombo:
I-American Lung Association. Pulmonary Fibrosis.
IThala leSizwe leMicrothelo. MedlinePlus. Pulmonary Fibrosis. Updated 07/13/16.