Kwayar cutar Von Hippel-Lindau (VHL) wani yanayi ne wanda ke haifar da ci gaban jini a cikin sassa daban-daban na jikinka. Wadannan ciwo masu maganganu zasu iya bunkasa cikin ciwon sukari da kuma cysts. VHL yana haifar da maye gurbi a cikin kwayar halittar da ke jagorancin ci gaban kwayar halitta, wanda ke samuwa a karo na uku na chromosome.
Dukkan maza da mata na kowace kabila suna fama da VHL, tare da kimanin 1 cikin 36,000 suna da yanayin.
Yawancin mutane sun fara fuskantar bayyanar cututtuka a cikin shekaru 23, kuma, a matsakaici, sun sami ganewar asali ta wurin lokacin da suka kasance 32.
Cutar cututtuka
Yawancin ciwon sukari da VHL ke haifarwa ba su da kyau amma zasu iya zama m. Tumau masu yawanci suna cikin:
- Eyes. Da ake kira hemangioblastomas (masu yawan jini), waɗannan ciwace-ciwacen ba ƙari ba ne amma zai iya haifar da matsaloli a cikin ido kamar farfadowar hangen nesa da karuwa da ido ( glaucoma ).
- Brain. Da aka sani da hemangioblastomas (yawancin jini), waɗannan mutane ba ƙyama ba ne amma na iya haifar da bayyanar cututtuka (kamar wahalar tafiya) saboda matsin da suke sanyawa a jikin kwakwalwa.
- Koda. Wadannan talakawa sune wadanda zasu iya zama mummunan rauni. Irin wannan ciwon daji, wanda ake kira karamin jini , shine babban dalilin mutuwar mutane da VHL.
- Adrenal gland. Da ake kira pheochromocytomas, ba yawanci ba ne amma zai iya haifar da karin adrenaline.
- Pancreas. Wadannan ciwace-ciwacen da yawa ba yawanci ba ne, amma kuma, a wasu lokuta, zasu cigaba da zama ciwon daji.
Hakanan na iya zamawa a cikin kashin baya, kunnuwa a ciki, dabbar genital, huhu, da hanta. Wasu mutane na iya samun ciwace-ciwace a wani yanki yayin da wasu zasu iya shafawa a yankuna masu yawa. Kashi 10 cikin dari na mutanen da ke dauke da VHL sukan inganta ƙwayar ciwon ƙwayoyi.
Ya kamata a kula da ciwon daji na ci gaba don hana tsararre.
Samun Bincike
Gwaran kwayoyin, ta hanyar gwajin jini , shine hanya mafi inganci na bincikar VHL. Idan iyayenku na da VHL, to, akwai damar kashi 50 cikin dari da kuka gaji yanayin. Duk da haka, ba duk lokuta na VHL an gaji ba. Kusan, kashi 20 cikin dari na VHL suna da maye gurbin kwayar da ba'a ƙetare daga iyayensu ba. Idan kana da VHL, akwai wata babbar dama da za ka ci gaba da akalla ƙwayar tumatir a rayuwarka - kashi 97 cikin dari na ciwon daji na ci gaba kafin cigaba da shekaru 60.
Jiyya
Zaɓuɓɓukan jiyya suna dogara ne akan inda tarin ku yake. Yawancin ciwace-ciwacen ƙwayoyi za a iya cire su tare da tiyata Wasu basu buƙatar cire su ba sai dai idan suna haifar da alamar cututtuka (misali, ƙwaƙwalwar ƙwaƙwalwar kwakwalwa a kwakwalwarka).
Idan kuna da VHL, kuna buƙatar samun gwaje-gwaje na jiki sau da yawa, kazalika da hotunan haɓaka mai kwakwalwa ( MRI ) ko ƙididdigar hoto ( CT ) na kwakwalwa, ciki, da kodan don kallon sababbin ciwace-ciwacen ƙwayoyi. Dole ne a gudanar da nazarin idanu akai-akai.
Dole a rufe wani kusa agogo a kan kowane kaya koda. Wadannan za a iya cire su a hankali don rage hadarin bunkasa ciwon koda. Kusan, kashi 70 cikin dari na mutanen da ke tare da VHL sukan inganta ciwon koda a cikin shekaru 60.
Duk da haka, idan cutar ciwon koda ba ta ci gaba ba, to, akwai kyawawan dama ba zai faru ba.
Sources:
Evans, JP (2002). von Hippel-Lindau cuta. eMedicine, isa ga http://www.emedicine.com/ped/topic2417.htm
VHL Alliance (2016). VHL Facts ,. http://vhl.org/about/resources/vhl-facts/