Malignant melanoma - I-Melanoma Enobungozihttps://en.wikipedia.org/wiki/Melanoma
I I-Melanoma Enobungozi (Malignant melanoma) luhlobo lomhlaza wolusu osuka kwiiseli ezivelisa umbala owaziwa ngokuba ziimelanocytes. Kwabasetyhini, zixhaphake kakhulu emilenzeni, ngelixa kumadoda, ngokuqhelekileyo zenzeka ngasemva. Malunga ne-25% ye-melanomas ivela kwi-nevus. Utshintsho kwi-nevi olunokuthi lubonise i-melanoma lubandakanya ukwanda kobukhulu, imiphetho engaqhelekanga, ukutshintsha kombala, okanye isilonda.

Oyena nobangela uphambili wemelanoma kukuvezwa kokukhanya kweultraviolet kwabo banamanqanaba asezantsi ebala lesikhumba imelanin (abemi abamhlophe). Ukukhanya kwe-UV kusenokuba kuvela elangeni okanye kwizixhobo zokutshisa. Abo bane-nevus ezininzi, imbali ye-melanoma yamalungu osapho, kunye nokungasebenzi kakuhle kwamajoni omzimba basengozini enkulu ye-melanoma.

Ukusebenzisa i-sunscreen kunye nokuphepha ukukhanya kwe-UV kunokuthintela i-melanoma. Unyango ludla ngokususwa ngotyando. Kwezo zinemihlaza emikhudlwana, ii-lymph nodes ezikufutshane zinokuvavanyelwa ukusasazeka (metastasis). Uninzi lwabantu luyanyangeka ukuba i-metastasis ayizange yenzeke. Kwabo basasazeke kubo i-melanoma, i-immunotherapy, unyango lwe-biologic, unyango lwe-radiation, okanye i-chemotherapy inokuphucula ukusinda. Ngonyango, amazinga okusinda kweminyaka emihlanu e-United States yi-99% phakathi kwabo banesifo sendawo, i-65% xa isifo sisasazekile kwii-lymph nodes, kunye ne-25% phakathi kwabo basasazeka kude.

Imelanoma lolona hlobo luyingozi lomhlaza wolusu. IOstreliya neNew Zealand zinezinga eliphezulu lemelanoma ehlabathini. Amazinga aphezulu emelanoma ayenzeka kuMntla Yurophu nakuMntla Melika. Imelanoma ayifumaneki kangako eAsia, eAfrika naseLatin America. EUnited States, imelanoma yenzeke malunga nezihlandlo ezili-1,6 kumadoda kunamabhinqa.

Iimpawu kunye neempawu
Iimpawu zokuqala ze-melanoma lutshintsho kwimilo okanye kumbala we-nevus ekhoyo. Kwimeko ye-nodular melanoma, kukubonakala kweqhuma elitsha esikhumbeni. Kwinqanaba lokugqibela le-melanoma, i-nevi inokurhawuzelelwa, ibe nesilonda, okanye yophe.

[A-Asymmetry] I-asymmetry yobume
[B-Borders] Umda (ngokungaqhelekanga kunye neekona kunye neekona)
[C-Color] Umbala (i-variegated kwaye ayiqhelekanga)
[D-Diameter] Ububanzi (ngaphezulu kwe-6 mm = 0.24 intshi = malunga nobukhulu bento yokucima ipensile)
[E-Evolving] Hlaziya ngokuhamba kwexesha

cf) I-Seborrheic keratosis inokuhlangabezana nezinye okanye zonke iikhrayitheriya ze-ABCD, kwaye inokukhokelela kwiialamu zobuxoki.

I-Metastasis ye-melanoma yokuqala inokwenzeka, kodwa inqabile; ngaphantsi kwesihlanu seemelanoma ezifunyaniswe kwangethuba zibe yimetastatic. Iimetastases zobuchopho zixhaphakile kwizigulane ezine-metastatic melanoma. I-Metastatic melanoma inokusasazeka kwisibindi, amathambo, isisu, okanye i-lymph nodes ezikude.

Uxilongo
Ukujonga indawo ekuthethwa ngayo yeyona ndlela ixhaphakileyo yokurhanela imelanoma. IiNevus ezingaqhelekanga ngombala okanye imilo zidla ngokuphathwa njengabagqatswa bemelanoma.
Oogqirha baphonononga zonke iimoles, kubandakanywa nezo zingaphantsi kwe-6 mm ububanzi. Xa isetyenziswe ziingcali eziqeqeshiweyo, i-dermoscopy inceda ngakumbi ukuchonga izilonda ezinobungozi kunokusebenzisa iliso lodwa. Uxilongo lwe-biopsy yaso nasiphi na isilonda solusu esineempawu zokuba sinokuba nomhlaza.

Unyango
#Mohs surgery

Ugqirha wakho unokuncoma i-immunotherapy ngakumbi ukuba unenqanaba lesi-3 okanye i-4 melanoma engenakususwa ngotyando.
#Ipilimumab [Yervoy]
#Pembrolizumab [Keytruda]
#Nivolumab [Opdivo]
☆ Kwiziphumo zika-2022 ze-Stiftung Warentest ezivela eJamani, ukwaneliseka kwabathengi ngeModelDerm bekungaphantsi kancinci kunokubonisana nge-telemedicine ehlawulweyo.
  • I-melanoma emalunga ne-2.5cm (1 intshi) ngo-1.5cm (0.6 intshi)
  • Malignant Melanoma ― ithanga lasekunene eliphakathi. I-Seborrheic keratosis inokuqwalaselwa njengoxilongo oluhlukileyo.
  • Malignant Melanoma in situ ― Igxalaba eliPhambili. Nangona imilo yesilonda i-asymmetric, ichazwa kakuhle kunye nombala olinganayo. Kwabase-Asiya, esi silonda sibonakala njenge-lentigo enobungozi, kodwa kufuneka kufuneke i-biopsy kubantu baseNtshona.
  • Malignant Melanoma ― Isilonda esingasemva. Kwabase-Asiya, ifunyaniswa kakhulu njenge-lentigo, kodwa i-biopsy kufuneka yenziwe kubantu baseNtshona.
  • Enkulu acral lentiginous melanoma ― Kwabase-Asiya, acral melanoma entendeni kunye neyodwa ixhaphakile, kanti kumazwe aseNtshona, imelanoma kwiindawo ezichaswe lilanga ixhaphake kakhulu.
  • I-black plaque ethambileyo ejikeleze isilonda yinto eqhelekileyo kwi- acral melanoma.
  • Indawo emnyama eye yahlasela indawo ye-matrix ye-nail ngaphandle kwesikhonkwane ibonisa ububi.
  • Amelanotic melanoma phantsi kwesikhonkwane yinto enqabileyo. Kubantu abadala abanokukhubazeka okungaqhelekanga, i-biopsy inokuqwalaselwa ukujonga zombini i-melanoma kunye ne-squamous cell carcinoma.
  • Nodular melanoma
  • Amelanotic Melanoma ― Ngasemva kwethanga. Abantu abalusu olulungileyo bahlala benesilonda sika- lightly pigmented or amelanotic melanomas. Lo mzekelo awubonisi utshintsho oluqaphelekayo lwemibala okanye ukwahluka.
  • Scalp ― Kwabase-Asiya, iimeko ezinjalo ziqhele ukufunyaniswa njenge-benign lentigo (hayi i-melanoma). Nangona kunjalo, amabala amakhulu anemibala kwiindawo ezibekwe elangeni afuna i-biopsy kubantu baseNtshona.
  • Malignant Melanoma ― forearm. Isilonda sibonisa i-asymmetric shape kunye nomda ongaqhelekanga.
  • Malignant Melanoma in situ ― Umphambili.
  • Malignant melanoma kumqolo ophakathi. Ubukho bebala lezilonda bubonisa imelanoma okanye i-basal cell carcinoma.
  • Melanoma ngenyawo. Ubume be-asymmetric kunye nombala, kunye nokudumba okukhaphayo kubonisa i-melanoma.
  • Acral melanoma ― Nail in Asiaans. Isiziba esimnyama esingaqhelekanga esidlulela ngaphaya kwesikhumba esiqhelekileyo esijikeleze isikhonkwane sisiphumo esibalulekileyo esicebisa ngamandla ububi.
  • Nangona le meko yafunyaniswa njenge-melanoma, ukufunyaniswa okubonakalayo kufana kakhulu ne-hematoma ye-nail. I-hematomas yezikhonkwane (benign) idla ngokunyamalala kwisithuba senyanga enye ukuya kwezimbini njengoko ikhutshelwa ngaphandle. Ngoko ke, ukuba isilonda sihlala ixesha elide, i-melanoma inokukrokra kwaye i-biopsy kufuneka yenziwe.
  • Amelanotic nodular melanoma ― Ukubonakaliswa okungaqhelekanga kwemelanoma.
References Malignant Melanoma 29262210 
NIH
I-melanoma luhlobo lwethumba elenzeka xa i-melanocytes iba yingozi. I-Melanocytes ivela kwi-neural crest. Oku kuthetha ukuba i-melanomas ayinakukhula kuphela eluswini kodwa nakwezinye iindawo apho iiseli ze-neural crest zihamba khona, njengephecana lesisu kunye nengqondo. Izigulana ezinenqanaba le-0 melanoma zinezinga lokusinda leminyaka emihlanu lama-97%, kanti abo banesifo senqanaba le-IV banomlinganiselo omalunga ne-10% kuphela.
A melanoma is a tumor produced by the malignant transformation of melanocytes. Melanocytes are derived from the neural crest; consequently, melanomas, although they usually occur on the skin, can arise in other locations where neural crest cells migrate, such as the gastrointestinal tract and brain. The five-year relative survival rate for patients with stage 0 melanoma is 97%, compared with about 10% for those with stage IV disease.
 European consensus-based interdisciplinary guideline for melanoma. Part 1: Diagnostics: Update 2022 35570085
Cutaneous melanoma (CM) luhlobo oluyingozi kakhulu lwethumba lolusu, elinoxanduva lokufa komhlaza wolusu i90%. Ukulungisa oku, iingcaphephe ezisuka kwi the European Dermatology Forum (EDF) , the European Association of Dermato-Oncology (EADO) , and the European Organization for Research and Treatment of Cancer (EORTC) ziye zasebenzisana.
Cutaneous melanoma (CM) is a highly dangerous type of skin tumor, responsible for 90% of skin cancer deaths. To address this, experts from the European Dermatology Forum (EDF), the European Association of Dermato-Oncology (EADO), and the European Organization for Research and Treatment of Cancer (EORTC) had collaborated.
 Immunotherapy in the Treatment of Metastatic Melanoma: Current Knowledge and Future Directions 32671117 
NIH
I<em>melanoma, uhlobo lomhlaza wolusu, ibalasele ngolwalamano olusondeleyo nenkqubo yomzimba yokuzikhusela. Oku kubonakala kukwanda kokwenzeka kwayo kubantu abanamajoni omzimba abuthathaka, ubukho beeseli zokhuselo lomzimba kuwo omabini amathumba okuqala kunye nokusasazeka kwawo kwamanye amalungu omzimba, kunye nenyaniso yokuba amajoni omzimba anokuqonda iiproteni ezithile ezifumaneka kwiiseli zemelanoma. Okubalulekileyo, unyango olomeleza amajoni omzimba lubonise isithembiso ekulweni nemelanoma. Ngelixa ukusetyenziswa konyango lokomeleza i-immune ekuphatheni i-melanoma ephezulu luphuhliso lwamva nje, uphando lwakutsha nje lubonisa ukuba ukudibanisa olu nyango kunye ne-chemotherapy, i-radiotherapy, okanye unyango olujoliswe kuyo lweemolekyuli lunokuphucula kakhulu iziphumo. Nangona kunjalo, i-immunotherapy enjalo inokubangela uluhlu lweziphumo ebezingalindelekanga ezinxulumene nomzimba ezichaphazela izitho ezahlukeneyo, ezinokunciphisa ukusetyenziswa kwayo. Ukujonga phambili, iindlela ezizayo zokunyanga imelanoma ephucukileyo zinokubandakanya unyango olujolise kwiindawo ezithile zokugonywa komzimba ezifana ne-PD1, okanye amachiza aphazamisana neendlela ezithile zeemolekyuli ezifana ne-BRAF kunye ne-MEK.
Melanoma is one of the most immunologic malignancies based on its higher prevalence in immune-compromised patients, the evidence of brisk lymphocytic infiltrates in both primary tumors and metastases, the documented recognition of melanoma antigens by tumor-infiltrating T lymphocytes and, most important, evidence that melanoma responds to immunotherapy. The use of immunotherapy in the treatment of metastatic melanoma is a relatively late discovery for this malignancy. Recent studies have shown a significantly higher success rate with combination of immunotherapy and chemotherapy, radiotherapy, or targeted molecular therapy. Immunotherapy is associated to a panel of dysimmune toxicities called immune-related adverse events that can affect one or more organs and may limit its use. Future directions in the treatment of metastatic melanoma include immunotherapy with anti-PD1 antibodies or targeted therapy with BRAF and MEK inhibitors.