Ukukhubazeka Kwegazi Lokuvimbela Igazi
I-Klippel-Trenaunay-Weber syndrome (i-KTW), eyaziwa nangokuthi i-Parkes-Weber syndrome, iyisifo segazi esiyisisindo esivela ekuzalweni. Abacwaningi abaqiniseki ukuthi kungani kwenzeka ngoba akubonakali kudluliswa ngokwezakhi zofuzo. Isifo se-Klippel-Trenaunay-Weber sithinta kokubili abesilisa nabesifazane. Ayaziwa ukuthi kwenzeka kaningi kangakanani.
Izimpawu
Izimpawu ze-KTW syndrome zingabandakanya:
- Isakhiwo esikhulu sokubeletha se-port-wine (ngokuvamile isibonakaliso sokuqala esiqaphele) esibangelwa imithwalo encane yegazi ngaphansi kwesikhumba. Kungenzeka kube obomvu obomvu, obomvu, ukuvuswa, noma okumele kube ne-bumps kuso ekhanda kalula. Ngokuvamile kuvame ukuthi iwayini le-port likhulu futhi kusukela i-KTW syndrome ivame ukuthinta umlenze (izikhathi ezintathu ngaphezu kwamanye izingxenye), isibonakaliso sokubeletha sihlanganisa, kusukela kwesisindo nesikhumba kuya ohlangothini oluthintekile lomzimba.
- ama-hemangiomas - amasosha angavamile emithanjeni yegazi
- i-varicose veins
- amathaneli emithanjeni yegazi ebizwa ngokuthi i-arteriovenous malformations (AVMs)
- ukukhula ngokweqile kwezicubu ezithambile nethambo emlenzeni othintekile
Izinkinga zamanzi ezitshalo kanye nokukhuphuka kwegazi kuholela ekuguleni, ubuhlungu, izifo zesikhumba (cellulitis), ukuhamba nobunzima, kanye nama-blood clots (okungase aqede ukujikeleza kwegazi emlenzeni, noma ukuya kwezinye izingxenye zomzimba futhi kubangele ukulimala). Umuntu ngamunye one-Klippel-Trenaunay-Weber syndrome uyathinteka ngendlela yakhe, futhi izinkinga ezihlangenwe nakho zingase zingakhululekile ukukhubaza kanzima.
Izimbangela ezimbili zegazi ezingenayo izibonakaliso ezifanayo yi-Klippel-Trenaunay syndrome ne- Sturge-Weber syndrome . Zombili zenza i-port port ne-blood container malformations. Kodwa-ke, ngokungafani ne-Klippel-Trenaunay syndrome, i-Parkes-Weber syndrome ne-Sturge-Weber syndrome ihlanganisa i-AVM futhi kungenzeka ukuthi ibe namandla kakhulu ngezimpawu ezinzima kakhulu.
Ukuxilongwa
Izimpawu ze-Klippel-Trenaunay-Weber syndrome zikhona lapho zizalwa. Ukuxilongwa kusekelwe ezimpawu, ikakhulukazi ukuba khona kwethebula lewayini lechweba nokukhula ngokweqile kwezicubu ezithambile noma amathambo. I- CT scan ne- MRI ziyasiza ekunqumeni ubukhulu be-syndrome.
Ukwelapha
Ukwelashwa kwe-KTW syndrome kugxile ezimpawu. Abantu abaningi basizwa izifo ezilula ezifana nezindwangu zokuxilonga, ezinciphisa ubuhlungu nokuvuvukala. Ukwelashwa kwe-Laser kunganciphisa noma kuqede i-port stain stain. Ngezinye izikhathi ukuhlinzwa kuyadingeka ukususa i-hemangioma enkulu noma ukususa izicubu ezingaphezu komlenze osondelene kakhulu. Ezimweni ezingavamile, umlenze othintekile ungadinga ukuba unqunywe ngenxa yezindwangu zegazi noma ukukhuphuka okukhulu.
Naphezu kokulimaza nokubuhlungu, abantu abaningi abane-Klippel-Trenaunay-Weber syndrome benza kahle ngokuphathwa kabi. Ukuhlinzwa kuyadingeka kuphela ezimweni ezimbi.
Umthombo:
> "Incazelo ye-Klippel-Trenaunay Syndrome." Ukuqonda i-Klippel-Trenaunay Syndrome. Iqembu le-Klippel-Trenaunay Syndrome Support. 26 Meyi 2009