I-Sturge-Weber syndrome yinkinga yesikhumba nesistimu yezinzwa. Isibonakaliso saso esivela kakhulu siwu-pink okhanyayo ekujuleni kwesizinda esibucayi esibucayi ebusweni obubizwa ngokuthi i-port stain stain. Noma kunjalo, akubona bonke abantu abane-stain wine stain abanesifo se-Sturge-Weber. I-Sturge-Weber syndrome ikhona lapho izalwa, kodwa aziwa ukuthi yini ebangela ukuthi yenzeke noma impela ukuthi kwenzeka kaningi kangakanani.
Lithinta kokubili abesilisa nabesifazane bazo zonke izizinda ezihlukahlukene.
Kunezinhlobo ezintathu ze-Sturge-Weber syndrome:
- Thayipha I - uhlobo oluvame kakhulu, luhlanganisa i-port stain stain kanye ne-angiomas yobuchopho
- Uhlobo lwesibili - iwayini lesiphathi se-port kodwa akukho-angioma yobuchopho
- Uhlobo III - ingqondo ye-angioma kodwa ayikho i-port wine stain
Izimpawu
Izimpawu ze-Sturge-Weber syndrome zifaka:
- Ithebula lewayini le-Port - Lesi sikhangiso sokuzalwa ebusweni singahluka ngobukhulu, kodwa ngokuvamile sihlanganisa okungenani ijwabu leso eliphakeme nekhanda. Ingahle ibonakale ukusuka ekukhanyeni okukhanyayo kuze kube yilabo abomvu obomvu futhi ibangelwa ukukhula ngokweqile kwemithambo yegazi encane (i-capillaries) ngaphansi nje kwesikhumba. Ithebula lewayini le-port lingase libe nzima ukubona abantu abanobomvu.
- Ukuhlukunyezwa - Amaphesenti angaba ngu-75 kuya kwangu-90 abantu abane-Sturge-Weber syndrome bahlaselwa, ngokuvamile baqala unyaka owodwa ubudala. Ukuqothulwa kubangelwa ukukhula ngokweqile kwemithambo yegazi (angioma) ebusweni bobuchopho, ngokuvamile ngemuva kwengqondo ehlangothini olufanayo njenge-wine stain stain.
- Ubuthakathaka - Amaphesenti angaba ngu-25 kuya ku-56 abantu abakha ubuthakathaka noma ukulahlekelwa ukusetshenziswa kolunye uhlangothi lomzimba (hemiparesis), ngokuvamile ohlangothini olubhekene nebala lewayini lechweba.
- Ukulibaziseka okuthuthukisayo nokulinda kwengqondo kuthinta amaphesenti angama-50 kuya kwangu-60 abantu.
- Izinsizwa
- Ukucindezela okwandayo iso (i-glaucoma) - Cishe amaphesenti angu-70 abantu ahlakulela i-glaucoma eseduze ne-stain wine stain.
Ukuxilongwa
Ukuxilongwa kwe-Sturge-Weber syndrome kungase kuphakanyiswe ukuba khona kwetayela lewayini le-port ngaphezu kwelinye nelinye ebunzini. Ukuskena kwe-Computed tomography (CT) noma i-imaging magnetic resonance (MRI) ingahlola ubuchopho ukuba khona kwe-angiomas eyodwa noma ngaphezulu, okuzoqinisekisa ukuxilongwa. Ingane ene-Sturge-Weber syndrome iyoba nokuhlolwa kwezinzwa ukuze kuhlolwe izinkinga ze-angioma yengqondo, njengokuhlukunyezwa noma ubuthakathaka.
Ukwelapha
Ukwelashwa kwe-Sturge-Weber syndrome kugxile ezimpawu. Uma ukuqubuka kwenzeka, imishanguzo ye-antiseizure efana ne-carbamazepine (i-Tegretol), i-phenytoin (i-Dilantin), noma i-valproic acid (i-Depakote, i-Depakene) inikezwa. Imithi isetshenziselwa ukunciphisa nokulawula i-glaucoma nekhanda. Ukwelashwa kwe-Laser kungakhanyisa noma kususe i-port stain stain ebusweni. Izindlela eziningi zokwelapha zingadingeka.
Umthombo:
> "Iyini i-Sturge-Weber Syndrome?" Mayelana ne-SWS / KT / PWS. Isisekelo se-Sturge-Weber. 10 Meyi 2007