Malignant Melanoma
Key facts
Malignant melanoma of the skin is a cancer that arises in melanocytes, the cells that produce the skin's pigment. It can develop within an existing mole or appear as a new pigmented lesion; the main subtypes are superficial spreading, nodular, lentigo maligna, and acral lentiginous melanoma. In men it is most often found on the trunk, head, or neck, while in women it forms most often on the arms and legs. The typical first sign is a change in a mole, summarized by the ABCDE rule: Asymmetry, irregular Border, uneven Color, Diameter larger than 6 mm, and Evolving appearance over time. Diagnosis is established by a skin examination and a biopsy of the lesion, examined under a microscope.
Prognosis
🔬 Histological Types
📚 Latest Research
Long-Term Outcomes Support Utilization of 23-GEP in Clinically Ambiguous Melanocytic Neoplasms.
Bal KS, et al
A real-world cohort study of 267 clinically ambiguous melanocytic lesions with a median 6-year follow-up found that the 23-gene expression profile (23-GEP) test successfully guided a definitive diagnosis in 89.5% of difficult-to-diagnose cases. Event rates (recurrence or metastasis) were 11.5% for lesions with malignant 23-GEP results, 2.9% for intermediate results, and only 1.3% for benign results, a difference that was highly statistically significant (Fisher exact, P = 0.002). These outcomes remained consistent in the subgroup of 163 lesions with at least 5 years of follow-up or a recorded event (P = 0.007). The findings provide robust long-term real-world validation that 23-GEP testing meaningfully stratifies oncological risk and can guide clinical management decisions for patients with otherwise indeterminate melanocytic lesions.
The American Journal of dermatopathology
Source →[Analysis of therapeutic effects of proton and heavy ion radiotherapy on uveal melanoma].
Yue H, et al
A retrospective study of 69 patients with uveal melanoma treated at Fudan University between 2015 and 2025 found that both proton beam therapy (12 patients, 17.4%) and heavy ion radiotherapy (57 patients, 82.6%) produced statistically significant tumor regression: the largest basal tumor diameter decreased from 11.3±2.9 mm to 9.5±3.5 mm and tumor thickness fell from 6.7±2.3 mm to 5.5±2.7 mm (both P<0.05). The eye preservation rate was high, with only 4 patients (5.8%) ultimately requiring enucleation, while 19 patients retained best-corrected visual acuity of ≥0.1 after treatment. The most common complications were radiation-induced retinopathy (42.0%), macular edema (37.7%), retinal detachment (34.8%), and cataracts (33.3%), a profile consistent with published particle-therapy benchmarks. These findings support particle radiotherapy — particularly heavy ion therapy — as an effective organ-preserving treatment for uveal melanoma in a Chinese clinical setting.
[Zhonghua yan ke za zhi] Chinese journal of ophthalmology
Source →Characteristics of plasma-activated water and its effect on apoptosis of malignant melanoma cells.
Chen M, et al
Plasma-activated water (PAW) generated by a helium atmospheric pressure plasma jet triggers mitochondrial apoptosis in malignant melanoma cells, with the longest irradiation treatment (PAW5, 5 minutes) producing the strongest cytotoxic effect. Researchers found that PAW treatment reduced B16 melanoma cell viability in a time-dependent manner, increased lactate dehydrogenase release, and elevated oxidative stress markers, including a rise in malondialdehyde (MDA) content and a progressive decline in superoxide dismutase (SOD) activity. Western blot analysis confirmed that PAW downregulated the anti-apoptotic protein Bcl-2, upregulated pro-apoptotic Bax, and activated cleaved caspase-9 and cleaved caspase-3, collectively pointing to the mitochondrial apoptotic pathway as the key mechanism. These results position PAW as a promising non-invasive therapeutic strategy for malignant melanoma that warrants further preclinical and clinical investigation.
Biochemical and biophysical research communications
Source →💊 Therapies
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🩺 Centers for this diagnosis
Warszawa, PL
OECI OECI treats this diagnosis
Białystok Oncology Centre
Cancer centerBiałystok, PL
CMJ treats this diagnosis
Prof. Franciszek Łukaszczyk Oncology Centre, Bydgoszcz
Cancer centerBydgoszcz, PL
CMJ treats this diagnosis
Greater Poland Cancer Centre, Poznań
Cancer centerPoznań, PL
OECI treats this diagnosis
West Pomeranian Oncology Centre in Szczecin
Cancer centerSzczecin, PL
CMJ treats this diagnosis
Show all centers for this diagnosis (17) ›
Centrum Medyczne HCP — Szpital im. św. Jana Pawła II, Poznań
Outpatient clinicPoznań, PL
treats this diagnosis
Mazovian Oncology Hospital — Warsaw
Outpatient clinicWarszawa, PL
treats this diagnosis
Radom Oncology Centre
Outpatient clinicRadom, PL
treats this diagnosis
Szpital na Klinach (Neo Hospital) — surgical oncology
Outpatient clinicKraków, PL
treats this diagnosis
Szpital św. Rafała — Scanmed (Kraków)
Outpatient clinicKraków, PL
treats this diagnosis
Dąbrowa Górnicza, PL
treats this diagnosis
Centrum Medycyny Profilaktycznej Salwator — Krakow
Outpatient clinicKrakow, PL
consults on this diagnosis
Centrum Medyczne Dekerta (Kraków)
Outpatient clinicKraków, PL
consults on this diagnosis
Inmedico Medical Centre, Tychy
Outpatient clinicTychy, PL
consults on this diagnosis
Krakowskie Centrum Diagnostyczno-Kliniczne (KCDK) — surgical oncology
Outpatient clinicKraków, PL
consults on this diagnosis
Onkomedica — Cancer Therapy Centre
Outpatient clinicWarszawa, PL
consults on this diagnosis
VEGAMED Regional Centre for Cancer Diagnosis and Treatment — Katowice
Outpatient clinicKatowice, PL
consults on this diagnosis