Algodystrophy: menene?

Algodystrophy: menene?

Ma'anar algodystrophy

THEalgodystrophy, kuma ake kira” reflex tausayi dystrophy ”Ko” hadaddun cututtukan yankin ciwo (SRDC) "wani nau'i ne na ciwo mai tsanani wanda yawanci yakan shafi hannu ko ƙafafu. Cuta ce da ba kasafai ba. Ciwo yana faruwa bayan karaya, busa, tiyata ko kamuwa da cuta.

Sanadin

Har yanzu ba a fahimci musabbabin algodystrophy ba. An yi imanin cewa suna cikin wani ɓangare saboda rashin aiki ko lalacewa ga tsarin juyayi na tsakiya (kwakwalwa da kashin baya) da na gefe (jijiya da ganglia).

Yawancin lokuta suna faruwa bayan rauni ga hannu ko ƙafa, kamar karaya ko yankewa. Tiyata, bugu, ƙwanƙwasa ko ma kamuwa da cuta kuma na iya haifarwa algodystrophy. Wani haɗari na cerebrovascular (CVA) ko ciwon zuciya na zuciya yana iya zama alhakin. Har ila yau damuwa na iya yin aiki a matsayin wani abu mai tsanani a cikin ciwo mai tsanani.

Nau'in algodystrophy na I, wanda ke shafar kashi 90% na lokuta, yana faruwa ne bayan rauni ko cuta wanda baya shafar jijiyoyi.

Nau'in algodystrophy na II yana haifar da lalacewa ga jijiyoyi a cikin nama da suka ji rauni.

Tsarin jima'i

Ana samun Algodystrophy a kowane zamani a cikin manya, a matsakaita kusan shekaru 40. Cutar ba kasafai take shafar yara da tsofaffi ba.

Cutar ta fi shafar mata fiye da maza. Muna magana ne game da mata 3 da abin ya shafa ga mutum 1.

Alamomin algodystrophy

Yawancin alamun farko na dystrophy da suka bayyana sune:

  • Wani ciwo mai tsanani ko soka mai kama da sandar allura da zafi mai zafi a hannu, hannu, kafa ko ƙafa.
  • Kumburi na yankin da abin ya shafa.
  • Hankalin fata don taɓawa, zafi ko sanyi.
  • Canje-canje a cikin nau'in fata, wanda ya zama bakin ciki, mai sheki, bushe da bushewa a kusa da yankin da abin ya shafa.
  • Canje-canje a yanayin zafin fata (mafi sanyi ko zafi).


Daga baya, wasu alamun bayyanar sun bayyana. Da zarar sun bayyana, galibi ba za su iya jurewa ba.

  • Canje-canje a launin fata daga jeri fari zuwa ja ko shuɗi.
  • Kauri, farce masu karye.
  • Ƙaruwar gumi.
  • Haɓaka ya biyo baya da raguwar gashi na yankin da abin ya shafa.
  • Tauri, kumburi sannan tabarbarewar gidajen abinci.
  • Muscle spasms, rauni, atrophy da wani lokacin ma tsoka contractures.
  • Asarar motsi a yankin da abin ya shafa.

Wani lokaci algodystrophy na iya yaduwa a wani wuri a cikin jiki, kamar kishiyar gaba. Ciwo na iya tsananta da damuwa.

A wasu mutane, bayyanar cututtuka na iya wuce watanni ko shekaru. A wasu kuma, suna tafiya da kansu.

Mutanen da ke cikin haɗari

  • Algodystrophy na iya nunawa a kowane zamani.
  • Wasu mutane suna da tsinkayar kwayoyin halitta don haɓaka algodystrophy.

hadarin dalilai

  •     Shan taba.

Ra'ayin likitan mu

THEalgodystrophy an yi sa'a cuta ce da ba kasafai ba. Idan, bayan rauni ko karaya zuwa hannu ko ƙafa, kun ci gaba da bayyanar cututtuka na algodystrophy (zaɓi mai tsanani ko ƙonawa, kumburin yankin da abin ya shafa, rashin jin daɗi don taɓawa, zafi ko sanyi), kada ku yi jinkirin tuntuɓar likitan ku kuma. . Matsalolin wannan cuta na iya zama mai matukar damuwa kuma suna haifar da ciwo mai tsanani. Duk da haka, da farko da aka yi amfani da maganin, mafi tasiri shine, ko ta hanyar shirin gyarawa ko kuma amfani da magunguna.

Dr Jacques Allard MD FCMF

 

 

Leave a Reply