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Yala an bɛna kuma Lynch Syndrome kan, o min bɛ dɔ fara kansɛri farati kan wa?

Yala an bɛna kuma Lynch Syndrome kan, o min bɛ dɔ fara kansɛri farati kan wa?

Yala aw delila ka Lynch Syndrome ko mɛn wa? Nin tɔgɔ in bɛ se ka kɛ ko kura ye dɔɔnin i bolo. Nka o ye jamu bana ye min bɛ bɔ mɔgɔw la ka taa mɔgɔw la, o bɛ dɔ fara an ka kansɛri sɔrɔli kan kosɛbɛ. O bɛ dɔ fara kansɛri sɔrɔli kan, kɛrɛnkɛrɛnnenya la sani aw ka se san 50. A ka ca a la, aw bɛ siran dɔɔni ni aw ye nin kumaw mɛn ko "aw bɛ se ka kansɛri sɔrɔ". Nka min nafa ka bon kosɛbɛ, o ye ka kunnafoni ɲuman sɔrɔ o cogoya suguw kan. O la bi an bɛna kuma nin kan nɔgɔya la, cogo la min bɛ se ka faamuya.

N’an y’a fɔ cogo nɔgɔman na, Lynch Syndrome ye mun ye?

Miiri k’a filɛ, an farikolo bɛ i n’a fɔ masin gɛlɛn dɔ min bɛ baara kɛ ka kɛɲɛ ni cikan gafe belebeleba dɔ ye (ADN). An ka jɛnɛya bɛ i n’a fɔ lɛtɛrɛ minnu bɛ nin kalan gafe kɔnɔ. Tuma dɔw la, filiw bɛ nin kalan gafe in kɔnɔ, walima ‘sɛbɛnni filiw’. Furakɛcogo la, o bɛ wele ko fɛn falen-falen jamu.

Lynch syndrome ye bana ye min bɛ sɔrɔ jamu jiginni fɛ. Jɛnkulu suguya kɛrɛnkɛrɛnnen dɔ bɛ an farikolo la min bɛ filiw dɔn ani k’u labɛn an ka ADN kɔnɔ. O bɛ wele ko ``mismatch repair (MMR)`` jamu. A bɛ i n'a fɔ ''dilanjɛkulu'' an farikolo la. Lynch ka bana bɛ mɔgɔ min na, fiɲɛ bɛ o ''dilanjɛkulu'' in ka jamu dɔ la. O la, fili minnu bɛ ADN kɔnɔ, olu tɛ dilan ka ɲɛ. Nin fili ninnu bɛ farikolokisɛ minnu na, olu bɛ ɲɔgɔn lajɛ ani waati tɛmɛnen kɔfɛ, u ka teli ka kɛ kansɛri ye.

Nin bana in bɛ se ka mɔgɔ bɛɛ minɛ. Sabula o ye bana ye min bɛ sɔrɔ jamu fɛ. Tuma dɔw la, aw bɛ se ka nin jamu nafama in ciyɛn ta ka bɔ aw ba walima aw fa fɛ. A man teli kosɛbɛ, o fɛn caman sɛgɛsɛgɛli bɛ se ka kɛ mɔgɔ kura farikolo la ni mɔgɔ si tɛ denbaya kɔnɔ. N’i ​​ye jatebɔw lajɛ jamana dɔ la i n’a fɔ Ameriki, a jateminɛna ko mɔgɔ 279 o 279, kelen ɲɔgɔn bɛ nin bana in sɔrɔ.

Lynch ka bana bɛ mɔgɔ min na, o bɛ se ka taamasiɲɛ jumɛnw sɔrɔ?

Fɛn min nafa ka bon ka kɔlɔsi yan, o ye ko Lynch ka bana taamasiɲɛ kɛrɛnkɛrɛnnen si tɛ a la. O nɔ na, ​​a ye kansɛriw taamasiɲɛ ye minnu bɛ sɔrɔ bana in fɛ. Olu la, kansɛri min ka teli ka kɛ, o ye kolotuguda kansɛri ye.

O la, taamasiɲɛ minnu ka teli ka sɔrɔ, olu dɔw filɛ nin ye minnu bɛ se ka kɛ ni kolotuguda kansɛri ye:

Taamaʃyɛn Cogojirali
Joli bɛ kɛ banakɔtaa laNɔgɔ bɛ se ka bilen walima ka kɛ nɛrɛmuguma ye ni joli ɲagaminen don a la.
Kɔnɔdimi walima kɔnɔboli Kɔnɔdimi walima dusukasi bɛ to ka kɛ a la.
Yɛlɛma donna banakɔtaa la Kɔnɔboli walima kɔnɔboli bɛ daminɛ yɔrɔnin kelen, walima banakɔtaa minnu ka fin ka tɛmɛ a cogo kɔrɔ kan.
Sɛgɛn min bɛ kɛ tuma caman na Sɛgɛn tuma bɛɛ hali ni lafiɲɛ ɲuman bɛ a la.
Funu walima funu A bɛ a ye ko a bɛ fa walima ka funu hali ni a ye dumuni dɔɔni dun.
Dusukunnata walima fɔɔnɔ Dusukunnata walima fɔɔnɔ min sababu jɛlen tɛ.

Min nafa ka bon, o ye ko bɛɛ tɛ nin taamasiɲɛ ninnu sɔrɔ. Tuma dɔw la, kansɛri bɛ se ka taamasiɲɛ foyi jira fo a ka jugu kosɛbɛ. O la, ni aw bɛ to ka nin taamasiɲɛ kelen walima caman sɔrɔ, aw ye aw jija ka taa dɔgɔtɔrɔso la walasa ka laadilikan sɔrɔ.

Kansɛri suguya jumɛnw bɛ se ka sɔrɔ nin bana in sababu fɛ?

Lynch syndrome tɛ bana ye min bɛ da wuli kansɛri suguya kelen dɔrɔn na. A bɛ dɔ fara kansɛri sɔrɔli kan farikolo yɔrɔ caman na. Farati bɛ farikolo yɔrɔ minnu na, olu bɛ se ka ɲɔgɔn ta ka kɛɲɛ ni jamu fililen ye. `MLHL`, `MSH2`, `MSH6`, `PMS2` ani `EPCAM` ye jɛnɛyaba duuru ye minnu bɛ o ko la.

Kansɛri suguya dɔw bɛ duguma, Lynch ka bana bɛ dɔ fara u farati kan.

Kansɛri suguya Farikolo yɔrɔ min bɛ tali kɛ o la
Kolotuguda ni kɔnɔbara kansɛri Dumunikɛcogo
Denso/Kɔnɔbara basigilen kansɛri Muso ka bangeko siratigɛ la
Ovarie kansɛri Muso ka bangeko siratigɛ la
Kɔnɔbara kansɛri Dumunikɛcogo
Banakɔtaa fitiniw kansɛri Dumunikɛcogo
Pankreyasi kansɛri Dumunikɛcogo
Sugunɛ sanfɛla kansɛri Sugunɛ kɛcogo
Sugunɛ kansɛri Nɛrɛmuguma
Fari kansɛri Golo

Kɔnɔbara kansɛri minnu bɛ sɔrɔ Lynch ka bana fɛ, olu tɛ kelen ye dɔɔni. U bɛ bonya joona kosɛbɛ ka tɛmɛ kansɛriw kan minnu bɛ sɔrɔ a cogo la.Hali ni a bɛ san 10 ɲɔgɔn ta walasa mɔgɔ gansan ka polipu fitini ka kɛ kansɛri ye, a bɛ san kelen walima san fila dɔrɔn de ta ni Lynch ka bana bɛ mɔgɔ min na.

Ani fana, ka da nin bana in kan, mɔgɔ min ye kolotuguda kansɛri sɔrɔ siɲɛ kelen, ka sɔrɔ ka kɛnɛya , o tigi ka kan ka kansɛri suguya kelen sɔrɔ tuguni.

Aw ye jateminɛ kɛ, kansɛri ka se ka segin ka kɛ 15% ɲɔgɔn ye san 10 kɔnɔ kansɛri fɔlɔ bɔlen kɔfɛ opereli fɛ. O farati bɛ se ka bonya ka se 40% ma san 20 kɔfɛ, ka se 60% ma san 30 kɔfɛ. O b’a jira ko sɛgɛsɛgɛli kɛli tuma bɛɛ nafa ka bon cogo min na.

O bɛ tɛmɛn cogo di mɔgɔw ni ɲɔgɔn cɛ?

Lynch syndrome ye bana ye min bɛ bɔ mɔgɔw la ka taa mɔgɔw la ``autosomal dominant`` cogo la. O kɔrɔ dɔrɔn ye ko hali ni bangebaga kelen dɔrɔn , ba walima fa, ka jamu nafama bɛ a la, a bɛ se ka kɛ 50% ye ko den bɛna o ciyɛn ta. O kɔrɔ ye ko den kelen-kelen bɛɛ bɛ se ka ciyɛn sɔrɔ 50% ani ka se ka ciyɛn sɔrɔ 50%.

O la, ni a sɔrɔla ko Lynch ka bana bɛ aw walima aw ka denbaya kɔnɔmɔgɔ dɔ la, a nafa ka bon kosɛbɛ aw ka aw ka denbaya tɔ ladɔnniya. Kɛrɛnkɛrɛnnenya la, o farati ka kan ka fɔ aw balimakɛw, aw denw ani aw bangebagaw ye. Ni i y’u bila ka taa u ka jamu sɛgɛsɛgɛli ni ladilikanw na, o bɛ se k’u ka ɲɛnamaya yɛrɛ kisi.

Ne bɛ se k’a dɔn cogo di ni nin bana in bɛ ne la? Ne ka kan ka sɛgɛsɛgɛli jumɛnw kɛ?

Lynch ka bana bɛ aw la , o cogo ɲuman ye ka jamu sɛgɛsɛgɛli kɛ . A ka c’a la, o bɛ kɛ ni joli ta ye. Walima da kɔnɔna na, aw bɛ da kɔnɔnatumu dɔ ta. Nin sɛgɛsɛgɛli in bɛ se k’a dɔn tigitigi ni fɛn dɔ b’i la an ye kuma minnu kan ka tɛmɛ, i n’a fɔ MLHL ni MSH2.

Ni a sɔrɔla ko Lynch ka bana bɛ aw la, min nafa ka bon kosɛbɛ o kɔfɛ, o ye ka sɛgɛsɛgɛli kɛ tuma bɛɛ walasa ka kansɛri dɔn joona. Aw ka dɔgɔtɔrɔ bɛna sɛgɛsɛgɛli kɛcogo dɔ labɛn min bɛ bɛn aw ma.

Kɔrɔbɔli A kɛcogo ani waati ladilikan
Kolonkɔni (kolonoscopie).Kolosinsinnan ye fɛɛrɛ ye min bɛ kɛ ni tubabufura finman dɔ don a kɔnɔ ni kamera ye ka tɛmɛ kɔnɔbara fɛ walasa ka kolotuguda sɛgɛsɛgɛ. a ka c' a la , a bɛ fɔ san o san walima san fila o san fila .
Ultrason ( Ultrason) min bɛ kɛ musoya fɛ Musow fɛ, a ka ɲi ka basibɔn sɛgɛsɛgɛli kɛ, o min ye ka sɛgɛsɛgɛlikɛlan dɔ don musoya fɛ ani ka denso ni kɔnɔbara lajɛ, o bɛ kɛ san fila o san walima san fila .
Sugunɛ sɛgɛsɛgɛli Aw bɛ faamuyali jɔnjɔn sɔrɔ sugunɛbilenni kansɛriw kan ni aw ye sugunɛ sɛgɛsɛgɛli kɛ. a ka ɲi ka o kɛ san o san .
Endoscopie supérieure (Endoscopie supérieure) ye Tubabukan min kɔnɔ kamera donna da la walasa ka kɔnɔbara ni banakɔtaa sanfɛla lajɛ. a bɛ fɔ san 3-5 o san 3-5 .
Biopsie (Biopsie) ye Ni farikolo yɔrɔ sikɛlen walima kuru dɔ sɔrɔla sanfɛla sɛgɛsɛgɛli senfɛ, a bɛ ta ka a lajɛ ni kansɛribana tɛ a la.

Lynch ka bana bɛ furakɛ cogo di?

Sisan, fura tɛ yen min bɛ Lynch syndrome jamu bana in furakɛ. O la, furakɛli kunba ye ka kansɛribanakisɛw dɔn ani k’u bɔ farikolo la opereli fɛ. Ni kansɛri bɛ se ka dɔn ka bɔ a la sani a ka jɛnsɛn farikolo yɔrɔ wɛrɛw la, o nɔ bɛ ɲɛ kosɛbɛ.

O bɛ dɔgɔtɔrɔw ka jɛkulu dɔ de wajibiya min bɛ baara kɛ ni fɛn caman ye. Misali la, kɔnɔboli dɔgɔtɔrɔw, operelikɛlaw, musow ka kansɛri dɔgɔtɔrɔw ani kansɛri dɔgɔtɔrɔw bɛ baara kɛ ɲɔgɔn fɛ walasa ka nin bana in furakɛ.

Mɔgɔ dɔw, kɛrɛnkɛrɛnnenya la muso minnu y’u ka denbaya dafa, olu b’a sugandi ka kɔnɔbara basigilen walima kɔnɔbara bɔli kɛ sani bana si ka daminɛ walasa ka dɔ bɔ u ka denso walima kɔnɔbara kansɛri sɔrɔli la don nataw la. O cogo kelen na, kolotuguda kansɛri farati ka bon mɔgɔ minnu na, olu bɛ se k’a sugandi ka kolotuguda lajɛ. Ninnu ye mɔgɔ yɛrɛ ka latigɛw ye kosɛbɛ, wa u ka kan ka kɛ baro caman kɛlen kɔfɛ ni dɔgɔtɔrɔ ye.

Yala Lynch syndrome ni HNPCC ye fɛn kelen ye wa?

N’a sɔrɔ aw ye tɔgɔ fana mɛn `HNPCC (Hereditary Non-Polyposis Colorectal Cancer)`. A ka ca a la, Lynch syndrome ni HNPCC bɛ kɛ ɲɔgɔn fɛ, nka danfara dɔɔnin bɛ u fila ni ɲɔgɔn cɛ fɛɛrɛko siratigɛ la.

N’an y’a fɔ cogo nɔgɔman na, HNPCC tɔgɔ bɛ fɔ ka da denbaya ka tariku kan. O kɔrɔ ye ko ni denbaya kɔnɔmɔgɔ damadɔw ye nin kansɛri suguya in sɔrɔ, a bɛ fɔ ko HNPCC bɛ o denbaya la. Nka Lynch syndrome ye tɔgɔ ye min bɛ da a kan , fɛn kɛrɛnkɛrɛnnen min bɛ kɛ sababu ye ka a sɔrɔ, o dɔnna. O la, HNPCC bɛ denbaya min na, o kɔnɔmɔgɔw bɛɛ bɛ se ka Lynch syndrome gène mutation sɔrɔ. Ani fana, mɔgɔ min ye jɛnɛya caman sɛnɛcogo kura sɔrɔ ni mɔgɔ wɛrɛ tɛ denbaya kɔnɔ, a bɛ se k’a fɔ fana ko Lynch ka bana bɛ o tigi la.

A man di mɔgɔ si ye ka nin kumaw mɛn ko: "Kansɛri bɛ i la." Lynch syndrome bɛ mɔgɔ min na, o tigi bɛ se ka o kumaw mɛn waati dɔ la a ka ɲɛnamaya kɔnɔ. Nka o tɛ diɲɛ laban ye. Ni aw bɛ aw ka bana dɔn, ka baara kɛ ni dɔgɔtɔrɔ ye, ani ka kansɛri sɛgɛsɛgɛli kɛ tuma bɛɛ, kansɛri suguya bɛɛ bɛ se ka dɔn ka kɛnɛya a daminɛ na. Ni aw ye a dɔn joona ani ka a furakɛ, o ye fɛɛrɛ ɲuman ye min bɛ se ka kɛ walasa ka ɲɛnamaya kɛ cogo la min bɛ kɛnɛya ni nisɔndiya la.

Take-Home cikan

  • Lynch syndrome ye bana ye min bɛ sɔrɔ jamu fɛ, min bɛ tɛmɛ mɔgɔw fɛ mɔgɔw fɛ, wa a bɛ dɔ fara kansɛri farati kan.
  • Hali ni nin jamu nafama in bɛ bangebaga kelen dɔrɔn de la, den bɛ se ka a ciyɛn sɔrɔ 50%.
  • Ni a sɔrɔla ko nin bana in bɛ aw walima aw ka denbaya kɔnɔmɔgɔ dɔ la, a nafa ka bon kosɛbɛ aw ka denbaya kɔnɔmɔgɔ gɛrɛgɛrɛ wɛrɛw ladɔnniya o ko la.
  • Hali ni o bana in tɛ se ka kɛnɛya, kansɛri kunbɛncogo ɲuman walima a dɔnni joona, o ye ka taa dɔgɔtɔrɔso la tuma bɛɛ.
  • Kansɛri sɔrɔli joona ani a furakɛli bɛ se ka kɛ sababu ye ka ɲɛtaa sɔrɔ kosɛbɛ ani ka a to i ka ɲɛnamaya kɛ kɛnɛya la.
  • Aw bɛ taa dɔgɔtɔrɔso la tuma bɛɛ walasa ka sɛgɛsɛgɛli kɛcogo dɔ sigi sen kan min bɛ bɛn aw ma ani ka haminanko o haminanko ɲɛnabɔ.

Lynch Syndrome, Kansɛri farati, Mutations genetiques, Kansɛri kolotuguda, Bana minnu bɛ sɔrɔ ciyɛn fɛ, Sɛgɛsɛgɛli genetique, Syndrome de Lynch

Frequently Asked Questions (FAQ)

Yala Lynch syndrome ni HNPCC ye fɛn kelen ye wa?

N’a sɔrɔ aw ye tɔgɔ fana mɛn `HNPCC (Hereditary Non-Polyposis Colorectal Cancer)`. A ka ca a la, Lynch syndrome ni HNPCC bɛ kɛ ɲɔgɔn fɛ, nka danfara dɔɔnin bɛ u fila ni ɲɔgɔn cɛ fɛɛrɛko siratigɛ la.

⚠️ Important: The medical articles and information on Nirogi Lanka are for general awareness only, and are by no means a substitute for professional medical advice, diagnosis, or treatment. For any medical problem you have, consult a qualified physician immediately.

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Yala an bɛna kuma Lynch Syndrome kan, o min bɛ dɔ fara kansɛri farati kan wa?
Kansɛri7 zuluye 2026

Yala an bɛna kuma Lynch Syndrome kan, o min bɛ dɔ fara kansɛri farati kan wa?

Yala aw delila ka Lynch Syndrome ko mɛn wa? Nin tɔgɔ in bɛ se ka kɛ ko kura ye dɔɔnin i bolo. Nka o ye jamu bana ye min bɛ bɔ mɔgɔw la ka taa mɔgɔw la, o bɛ dɔ fara an ka kansɛri sɔrɔli kan kosɛbɛ. O bɛ dɔ fara kansɛri sɔrɔli kan, kɛrɛnkɛrɛnnenya la sani aw ka se san 50. A ka ca a la, aw bɛ siran dɔɔni ni aw ye nin kumaw mɛn ko "aw bɛ se ka kansɛri sɔrɔ". Nka min nafa ka bon kosɛbɛ, o ye ka kunnafoni ɲuman sɔrɔ o cogoya suguw kan. O la bi an bɛna kuma nin kan nɔgɔya la, cogo la min bɛ se ka faamuya.

N’an y’a fɔ cogo nɔgɔman na, Lynch Syndrome ye mun ye?

Miiri k’a filɛ, an farikolo bɛ i n’a fɔ masin gɛlɛn dɔ min bɛ baara kɛ ka kɛɲɛ ni cikan gafe belebeleba dɔ ye (ADN). An ka jɛnɛya bɛ i n’a fɔ lɛtɛrɛ minnu bɛ nin kalan gafe kɔnɔ. Tuma dɔw la, filiw bɛ nin kalan gafe in kɔnɔ, walima ‘sɛbɛnni filiw’. Furakɛcogo la, o bɛ wele ko fɛn falen-falen jamu.

Lynch syndrome ye bana ye min bɛ sɔrɔ jamu jiginni fɛ. Jɛnkulu suguya kɛrɛnkɛrɛnnen dɔ bɛ an farikolo la min bɛ filiw dɔn ani k’u labɛn an ka ADN kɔnɔ. O bɛ wele ko ``mismatch repair (MMR)`` jamu. A bɛ i n'a fɔ ''dilanjɛkulu'' an farikolo la. Lynch ka bana bɛ mɔgɔ min na, fiɲɛ bɛ o ''dilanjɛkulu'' in ka jamu dɔ la. O la, fili minnu bɛ ADN kɔnɔ, olu tɛ dilan ka ɲɛ. Nin fili ninnu bɛ farikolokisɛ minnu na, olu bɛ ɲɔgɔn lajɛ ani waati tɛmɛnen kɔfɛ, u ka teli ka kɛ kansɛri ye.

Nin bana in bɛ se ka mɔgɔ bɛɛ minɛ. Sabula o ye bana ye min bɛ sɔrɔ jamu fɛ. Tuma dɔw la, aw bɛ se ka nin jamu nafama in ciyɛn ta ka bɔ aw ba walima aw fa fɛ. A man teli kosɛbɛ, o fɛn caman sɛgɛsɛgɛli bɛ se ka kɛ mɔgɔ kura farikolo la ni mɔgɔ si tɛ denbaya kɔnɔ. N’i ​​ye jatebɔw lajɛ jamana dɔ la i n’a fɔ Ameriki, a jateminɛna ko mɔgɔ 279 o 279, kelen ɲɔgɔn bɛ nin bana in sɔrɔ.

Lynch ka bana bɛ mɔgɔ min na, o bɛ se ka taamasiɲɛ jumɛnw sɔrɔ?

Fɛn min nafa ka bon ka kɔlɔsi yan, o ye ko Lynch ka bana taamasiɲɛ kɛrɛnkɛrɛnnen si tɛ a la. O nɔ na, ​​a ye kansɛriw taamasiɲɛ ye minnu bɛ sɔrɔ bana in fɛ. Olu la, kansɛri min ka teli ka kɛ, o ye kolotuguda kansɛri ye.

O la, taamasiɲɛ minnu ka teli ka sɔrɔ, olu dɔw filɛ nin ye minnu bɛ se ka kɛ ni kolotuguda kansɛri ye:

Taamaʃyɛn Cogojirali
Joli bɛ kɛ banakɔtaa laNɔgɔ bɛ se ka bilen walima ka kɛ nɛrɛmuguma ye ni joli ɲagaminen don a la.
Kɔnɔdimi walima kɔnɔboli Kɔnɔdimi walima dusukasi bɛ to ka kɛ a la.
Yɛlɛma donna banakɔtaa la Kɔnɔboli walima kɔnɔboli bɛ daminɛ yɔrɔnin kelen, walima banakɔtaa minnu ka fin ka tɛmɛ a cogo kɔrɔ kan.
Sɛgɛn min bɛ kɛ tuma caman na Sɛgɛn tuma bɛɛ hali ni lafiɲɛ ɲuman bɛ a la.
Funu walima funu A bɛ a ye ko a bɛ fa walima ka funu hali ni a ye dumuni dɔɔni dun.
Dusukunnata walima fɔɔnɔ Dusukunnata walima fɔɔnɔ min sababu jɛlen tɛ.

Min nafa ka bon, o ye ko bɛɛ tɛ nin taamasiɲɛ ninnu sɔrɔ. Tuma dɔw la, kansɛri bɛ se ka taamasiɲɛ foyi jira fo a ka jugu kosɛbɛ. O la, ni aw bɛ to ka nin taamasiɲɛ kelen walima caman sɔrɔ, aw ye aw jija ka taa dɔgɔtɔrɔso la walasa ka laadilikan sɔrɔ.

Kansɛri suguya jumɛnw bɛ se ka sɔrɔ nin bana in sababu fɛ?

Lynch syndrome tɛ bana ye min bɛ da wuli kansɛri suguya kelen dɔrɔn na. A bɛ dɔ fara kansɛri sɔrɔli kan farikolo yɔrɔ caman na. Farati bɛ farikolo yɔrɔ minnu na, olu bɛ se ka ɲɔgɔn ta ka kɛɲɛ ni jamu fililen ye. `MLHL`, `MSH2`, `MSH6`, `PMS2` ani `EPCAM` ye jɛnɛyaba duuru ye minnu bɛ o ko la.

Kansɛri suguya dɔw bɛ duguma, Lynch ka bana bɛ dɔ fara u farati kan.

Kansɛri suguya Farikolo yɔrɔ min bɛ tali kɛ o la
Kolotuguda ni kɔnɔbara kansɛri Dumunikɛcogo
Denso/Kɔnɔbara basigilen kansɛri Muso ka bangeko siratigɛ la
Ovarie kansɛri Muso ka bangeko siratigɛ la
Kɔnɔbara kansɛri Dumunikɛcogo
Banakɔtaa fitiniw kansɛri Dumunikɛcogo
Pankreyasi kansɛri Dumunikɛcogo
Sugunɛ sanfɛla kansɛri Sugunɛ kɛcogo
Sugunɛ kansɛri Nɛrɛmuguma
Fari kansɛri Golo

Kɔnɔbara kansɛri minnu bɛ sɔrɔ Lynch ka bana fɛ, olu tɛ kelen ye dɔɔni. U bɛ bonya joona kosɛbɛ ka tɛmɛ kansɛriw kan minnu bɛ sɔrɔ a cogo la.Hali ni a bɛ san 10 ɲɔgɔn ta walasa mɔgɔ gansan ka polipu fitini ka kɛ kansɛri ye, a bɛ san kelen walima san fila dɔrɔn de ta ni Lynch ka bana bɛ mɔgɔ min na.

Ani fana, ka da nin bana in kan, mɔgɔ min ye kolotuguda kansɛri sɔrɔ siɲɛ kelen, ka sɔrɔ ka kɛnɛya , o tigi ka kan ka kansɛri suguya kelen sɔrɔ tuguni.

Aw ye jateminɛ kɛ, kansɛri ka se ka segin ka kɛ 15% ɲɔgɔn ye san 10 kɔnɔ kansɛri fɔlɔ bɔlen kɔfɛ opereli fɛ. O farati bɛ se ka bonya ka se 40% ma san 20 kɔfɛ, ka se 60% ma san 30 kɔfɛ. O b’a jira ko sɛgɛsɛgɛli kɛli tuma bɛɛ nafa ka bon cogo min na.

O bɛ tɛmɛn cogo di mɔgɔw ni ɲɔgɔn cɛ?

Lynch syndrome ye bana ye min bɛ bɔ mɔgɔw la ka taa mɔgɔw la ``autosomal dominant`` cogo la. O kɔrɔ dɔrɔn ye ko hali ni bangebaga kelen dɔrɔn , ba walima fa, ka jamu nafama bɛ a la, a bɛ se ka kɛ 50% ye ko den bɛna o ciyɛn ta. O kɔrɔ ye ko den kelen-kelen bɛɛ bɛ se ka ciyɛn sɔrɔ 50% ani ka se ka ciyɛn sɔrɔ 50%.

O la, ni a sɔrɔla ko Lynch ka bana bɛ aw walima aw ka denbaya kɔnɔmɔgɔ dɔ la, a nafa ka bon kosɛbɛ aw ka aw ka denbaya tɔ ladɔnniya. Kɛrɛnkɛrɛnnenya la, o farati ka kan ka fɔ aw balimakɛw, aw denw ani aw bangebagaw ye. Ni i y’u bila ka taa u ka jamu sɛgɛsɛgɛli ni ladilikanw na, o bɛ se k’u ka ɲɛnamaya yɛrɛ kisi.

Ne bɛ se k’a dɔn cogo di ni nin bana in bɛ ne la? Ne ka kan ka sɛgɛsɛgɛli jumɛnw kɛ?

Lynch ka bana bɛ aw la , o cogo ɲuman ye ka jamu sɛgɛsɛgɛli kɛ . A ka c’a la, o bɛ kɛ ni joli ta ye. Walima da kɔnɔna na, aw bɛ da kɔnɔnatumu dɔ ta. Nin sɛgɛsɛgɛli in bɛ se k’a dɔn tigitigi ni fɛn dɔ b’i la an ye kuma minnu kan ka tɛmɛ, i n’a fɔ MLHL ni MSH2.

Ni a sɔrɔla ko Lynch ka bana bɛ aw la, min nafa ka bon kosɛbɛ o kɔfɛ, o ye ka sɛgɛsɛgɛli kɛ tuma bɛɛ walasa ka kansɛri dɔn joona. Aw ka dɔgɔtɔrɔ bɛna sɛgɛsɛgɛli kɛcogo dɔ labɛn min bɛ bɛn aw ma.

Kɔrɔbɔli A kɛcogo ani waati ladilikan
Kolonkɔni (kolonoscopie).Kolosinsinnan ye fɛɛrɛ ye min bɛ kɛ ni tubabufura finman dɔ don a kɔnɔ ni kamera ye ka tɛmɛ kɔnɔbara fɛ walasa ka kolotuguda sɛgɛsɛgɛ. a ka c' a la , a bɛ fɔ san o san walima san fila o san fila .
Ultrason ( Ultrason) min bɛ kɛ musoya fɛ Musow fɛ, a ka ɲi ka basibɔn sɛgɛsɛgɛli kɛ, o min ye ka sɛgɛsɛgɛlikɛlan dɔ don musoya fɛ ani ka denso ni kɔnɔbara lajɛ, o bɛ kɛ san fila o san walima san fila .
Sugunɛ sɛgɛsɛgɛli Aw bɛ faamuyali jɔnjɔn sɔrɔ sugunɛbilenni kansɛriw kan ni aw ye sugunɛ sɛgɛsɛgɛli kɛ. a ka ɲi ka o kɛ san o san .
Endoscopie supérieure (Endoscopie supérieure) ye Tubabukan min kɔnɔ kamera donna da la walasa ka kɔnɔbara ni banakɔtaa sanfɛla lajɛ. a bɛ fɔ san 3-5 o san 3-5 .
Biopsie (Biopsie) ye Ni farikolo yɔrɔ sikɛlen walima kuru dɔ sɔrɔla sanfɛla sɛgɛsɛgɛli senfɛ, a bɛ ta ka a lajɛ ni kansɛribana tɛ a la.

Lynch ka bana bɛ furakɛ cogo di?

Sisan, fura tɛ yen min bɛ Lynch syndrome jamu bana in furakɛ. O la, furakɛli kunba ye ka kansɛribanakisɛw dɔn ani k’u bɔ farikolo la opereli fɛ. Ni kansɛri bɛ se ka dɔn ka bɔ a la sani a ka jɛnsɛn farikolo yɔrɔ wɛrɛw la, o nɔ bɛ ɲɛ kosɛbɛ.

O bɛ dɔgɔtɔrɔw ka jɛkulu dɔ de wajibiya min bɛ baara kɛ ni fɛn caman ye. Misali la, kɔnɔboli dɔgɔtɔrɔw, operelikɛlaw, musow ka kansɛri dɔgɔtɔrɔw ani kansɛri dɔgɔtɔrɔw bɛ baara kɛ ɲɔgɔn fɛ walasa ka nin bana in furakɛ.

Mɔgɔ dɔw, kɛrɛnkɛrɛnnenya la muso minnu y’u ka denbaya dafa, olu b’a sugandi ka kɔnɔbara basigilen walima kɔnɔbara bɔli kɛ sani bana si ka daminɛ walasa ka dɔ bɔ u ka denso walima kɔnɔbara kansɛri sɔrɔli la don nataw la. O cogo kelen na, kolotuguda kansɛri farati ka bon mɔgɔ minnu na, olu bɛ se k’a sugandi ka kolotuguda lajɛ. Ninnu ye mɔgɔ yɛrɛ ka latigɛw ye kosɛbɛ, wa u ka kan ka kɛ baro caman kɛlen kɔfɛ ni dɔgɔtɔrɔ ye.

Yala Lynch syndrome ni HNPCC ye fɛn kelen ye wa?

N’a sɔrɔ aw ye tɔgɔ fana mɛn `HNPCC (Hereditary Non-Polyposis Colorectal Cancer)`. A ka ca a la, Lynch syndrome ni HNPCC bɛ kɛ ɲɔgɔn fɛ, nka danfara dɔɔnin bɛ u fila ni ɲɔgɔn cɛ fɛɛrɛko siratigɛ la.

N’an y’a fɔ cogo nɔgɔman na, HNPCC tɔgɔ bɛ fɔ ka da denbaya ka tariku kan. O kɔrɔ ye ko ni denbaya kɔnɔmɔgɔ damadɔw ye nin kansɛri suguya in sɔrɔ, a bɛ fɔ ko HNPCC bɛ o denbaya la. Nka Lynch syndrome ye tɔgɔ ye min bɛ da a kan , fɛn kɛrɛnkɛrɛnnen min bɛ kɛ sababu ye ka a sɔrɔ, o dɔnna. O la, HNPCC bɛ denbaya min na, o kɔnɔmɔgɔw bɛɛ bɛ se ka Lynch syndrome gène mutation sɔrɔ. Ani fana, mɔgɔ min ye jɛnɛya caman sɛnɛcogo kura sɔrɔ ni mɔgɔ wɛrɛ tɛ denbaya kɔnɔ, a bɛ se k’a fɔ fana ko Lynch ka bana bɛ o tigi la.

A man di mɔgɔ si ye ka nin kumaw mɛn ko: "Kansɛri bɛ i la." Lynch syndrome bɛ mɔgɔ min na, o tigi bɛ se ka o kumaw mɛn waati dɔ la a ka ɲɛnamaya kɔnɔ. Nka o tɛ diɲɛ laban ye. Ni aw bɛ aw ka bana dɔn, ka baara kɛ ni dɔgɔtɔrɔ ye, ani ka kansɛri sɛgɛsɛgɛli kɛ tuma bɛɛ, kansɛri suguya bɛɛ bɛ se ka dɔn ka kɛnɛya a daminɛ na. Ni aw ye a dɔn joona ani ka a furakɛ, o ye fɛɛrɛ ɲuman ye min bɛ se ka kɛ walasa ka ɲɛnamaya kɛ cogo la min bɛ kɛnɛya ni nisɔndiya la.

Take-Home cikan

  • Lynch syndrome ye bana ye min bɛ sɔrɔ jamu fɛ, min bɛ tɛmɛ mɔgɔw fɛ mɔgɔw fɛ, wa a bɛ dɔ fara kansɛri farati kan.
  • Hali ni nin jamu nafama in bɛ bangebaga kelen dɔrɔn de la, den bɛ se ka a ciyɛn sɔrɔ 50%.
  • Ni a sɔrɔla ko nin bana in bɛ aw walima aw ka denbaya kɔnɔmɔgɔ dɔ la, a nafa ka bon kosɛbɛ aw ka denbaya kɔnɔmɔgɔ gɛrɛgɛrɛ wɛrɛw ladɔnniya o ko la.
  • Hali ni o bana in tɛ se ka kɛnɛya, kansɛri kunbɛncogo ɲuman walima a dɔnni joona, o ye ka taa dɔgɔtɔrɔso la tuma bɛɛ.
  • Kansɛri sɔrɔli joona ani a furakɛli bɛ se ka kɛ sababu ye ka ɲɛtaa sɔrɔ kosɛbɛ ani ka a to i ka ɲɛnamaya kɛ kɛnɛya la.
  • Aw bɛ taa dɔgɔtɔrɔso la tuma bɛɛ walasa ka sɛgɛsɛgɛli kɛcogo dɔ sigi sen kan min bɛ bɛn aw ma ani ka haminanko o haminanko ɲɛnabɔ.

Lynch Syndrome, Kansɛri farati, Mutations genetiques, Kansɛri kolotuguda, Bana minnu bɛ sɔrɔ ciyɛn fɛ, Sɛgɛsɛgɛli genetique, Syndrome de Lynch

Frequently Asked Questions (FAQ)

Yala Lynch syndrome ni HNPCC ye fɛn kelen ye wa?

N’a sɔrɔ aw ye tɔgɔ fana mɛn `HNPCC (Hereditary Non-Polyposis Colorectal Cancer)`. A ka ca a la, Lynch syndrome ni HNPCC bɛ kɛ ɲɔgɔn fɛ, nka danfara dɔɔnin bɛ u fila ni ɲɔgɔn cɛ fɛɛrɛko siratigɛ la.

⚠️ Important: The medical articles and information on Nirogi Lanka are for general awareness only, and are by no means a substitute for professional medical advice, diagnosis, or treatment. For any medical problem you have, consult a qualified physician immediately.

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