What does cancer look like on skin? Below is a selection of photos that give you a general idea about what skin cancers can look like. Remember that skin cancers can look quite different from one person to another due to skin tone, size and type of skin cancer and location on the body. Skin cancer can be tricky in other ways, too. For example, melanoma is a type of skin cancer that is often pigmented tan, brown, black, even blue. But amelanotic melanoma lacks pigment and appears as a skin-tone or pink lesion.

Actinic keratosis (also known as solar keratosis) is the most common precancer. For more photos and information on actinic keratosis warning signs and symptoms, visit our Actinic Keratosis Warning Signs page.


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Our 24/7 cancer helpline provides information and answers for people dealing with cancer. We can connect you with trained cancer information specialists who will answer questions about a cancer diagnosis and provide guidance and a compassionate ear.

Our highly trained specialists are available 24/7 via phone and on weekdays can assist through video calls and online chat. We connect patients, caregivers, and family members with essential services and resources at every step of their cancer journey. Ask us how you can get involved and support the fight against cancer. Some of the topics we can assist with include:

The mission of the Cancer Imaging Program, National Cancer Institute, is to promote and support: Cancer-related basic, translational and clinical research in imaging sciences and technology, and integration and application of these imaging discoveries and developments to the understanding of cancer biology and to the clinical management of cancer and cancer risk. more >

The European Cancer Imaging Initiative is one of the flagships of the Europe's Beating Cancer Plan (EBCP). One of the objectives of the Plan is to make the most of the potential of data and digital technologies such as Artificial Intelligence (AI) or High-Performance Computing (HPC) to combat cancer.

The aim of the European Cancer Imaging Initiative is to foster innovation and deployment of digital technologies in cancer treatment and care, to achieve more precise and faster clinical decision-making, diagnostics, treatments and predictive medicine for cancer patients.

The Initiative will showcase how medical images can be accessed, used and pooled, while ensuring a high level of ethics, trust, security and personal data protection in full compliance with EU values and rules. It will make large amounts of cancer images and linked clinical data easily accessible to European clinicians, researchers and innovators in line with the European data strategy and supporting the goals of the European Health Data Space.

Cancer imaging datasets exist for different cancer types, but they are scattered among many repositories and clinical centres in Europe, and they are not easily accessible to clinicians, researchers and innovators.

The European Cancer Imaging Initiative will work towards linking up resources and databases to an open, available and user-friendly infrastructure of cancer images for all stakeholders. This will be achieved through an integrated approach designed with major European research organisations, institutions, and companies. The infrastructure will support the development and benchmarking, testing and piloting of tools for personalised medicine, essentially offering a backbone for next generation of cancer diagnostics and treatments.

The project will provide a central hub that will link EU-level and national initiatives, hospital networks as well as research repositories with cancer images data. Clinicians, researchers and innovators will have cross-border access to an interoperable, privacy-preserving and secure infrastructure for federated, distributed analysis of cancer imaging data.

EUCAIM plans to make cancer images data available to the AI Testing and Experimentation Facility for Health established under the DIGITAL programme. The TEF-Health project started in January 2023. This will allow small and medium-sized enterprises who have developed Artificial Intelligence solutions for cancer care to test them in real-life environments. Other testing facilities will also be considered.

Skin cancers -- including melanoma, basal cell carcinoma, and squamous cell carcinoma -- often start as changes to your skin. They can be new growths or precancerous lesions -- changes that are not cancer but could become cancer over time. An estimated 40% to 50% of fair-skinned people who live to be 65 will develop at least one skin cancer. Learn to spot the early warning signs. Skin cancer can be cured if it's found and treated early.

Related to actinic keratosis, actinic cheilitis is a precancerous condition that usually appears on the lower lips. Scaly patches or persistent roughness of the lips may be present. Less common symptoms include swelling of the lip, loss of the sharp border between the lip and skin, and prominent lip lines. Actinic cheilitis may evolve into invasive squamous cell carcinoma if not treated.

A mole (nevus) is a benign growth of melanocytes, cells that gives skin its color. Although very few moles become cancer, abnormal or atypical moles can develop into melanoma over time. "Normal" moles can appear flat or raised or may begin flat and become raised over time. The surface is typically smooth. Moles that may have changed into skin cancer are often irregularly shaped, contain many colors, and are larger than the size of a pencil eraser. Most moles develop in youth or young adulthood. It's unusual to acquire a mole in the adult years.

Atypical moles are not cancer, but they can become cancer. They can be found in sun-exposed or sun-protected areas of the body. Atypical moles may be larger (one-quarter inch across or larger) and more irregular in shape, with notched or fading borders. They may be flat or raised or the surface smooth or rough. They are typically of mixed color, including pink, red, tan, and brown.

Most moles on a person's body look similar to one another. A mole or freckle that looks different from the others or that has any characteristics of the ABCDEs of melanoma should be checked by a dermatologist. It could be cancerous. The ABCDEs are important characteristics to consider when examining your moles or other skin growths, so learn them in the slides to come.

If you find a mole or spot that has any ABCDE's of melanoma -- or one that's tender, itching, oozing, scaly, doesn't heal or has redness or swelling beyond the mole -- see a doctor. Your doctor may want to remove a tissue sample from the mole and biopsy it. If found to be cancerous, the entire mole and a rim of normal skin around it will be removed and the wound stitched closed. Additional treatment may be needed.

Malignant melanoma, especially in the later stages, is serious and treatment is difficult. Early diagnosis and treatment can increase the survival rate. Nonmelanoma skin cancers include basal cell carcinoma and squamous cell carcinoma. Both are common and are almost always cured when found early and treated. People who've had skin cancer once are at risk for getting it again; they should get a checkup at least once a year.

A melanoma is a form of skin cancer that develops in the cells (melanocytes) that produce the pigment that gives color to your skin, hair and eyes. The tumors usually contain melanin which makes them dark in color but in some cases, they can be free of any pigment. Melanomas spread quickly so it is important to identify and treat them quickly. They may be removed surgically, but immunotherapy (drug treatment to help your immune system fight the cancer), targeted therapy (targeted drug treatments that focus on weaknesses in the cancer cells), radiation therapy or chemotherapy (drugs to kill cancer cells) may be needed.

This nonmelanoma skin cancer may appear as a firm red nodule, a scaly growth that bleeds or develops a crust, or a sore that doesn't heal. It most often occurs on the nose, forehead, ears, lower lip, hands, and other sun-exposed areas of the body. Squamous cell carcinoma is curable if caught and treated early. If the skin cancer becomes more advanced, treatment will depend on the stage of cancer.

Bowen disease is also called squamous cell carcinoma "in situ." It is a type of skin cancer that spreads outward on the surface of the skin. By contrast, "invasive" squamous cell carcinomas can grow inward and spread to the interior of the body. Bowen disease looks like scaly, reddish patches that may be crusted; it may be mistaken for rashes, eczema, fungus, or psoriasis.

Basal cell carcinoma is the most common form of skin cancer caused by sun damage. BCC causes small bumps or open sores on the skin like this one. It is slow growing, and if not removed can spread into local underlying tissues.

Sun exposure is the biggest cause of skin cancer. But it doesn't explain skin cancers that develop on skin not ordinarily exposed to sunlight. Exposure to environmental hazards, radiation treatment, and even heredity may play a role. Although anyone can get skin cancer, the risk is greatest for people who have:

Nodular basal cell cancers can look see through (translucent) and shiny. You can often also see their blood vessels. Sometimes they have a sore (ulcerated) area and it may also have fluid filled sacs (cystic).

The basis for imaging tumour heterogeneity with CT is that misshapen, irregular, disorganized and tortuous architecture arising from tumour-induced angiogenesis eventually results in the formation of hypoxic voids, necrosis and an acidic milieu. These pathologic features have a fundamental role in tumorigenesis and this adverse microenvironment results in increased tumour invasion and metastasis, tumour tissue swelling, impaired delivery of chemotherapeutic agent, increased cellular resistance to chemotherapy and radiotherapy and inhibition of immune responses[36,37]. We postulate that heterogeneity measured on CT could potentially be a reflection of the above complex vascular environment seen within malignant neoplasms. This hypothesis is supported by previous clinical studies that have identified biological correlates for CTTA, confirming an association between CT heterogeneity and a hypoxic and angiogenic tumour microenvironment. Tumour heterogeneity at medium and coarse texture scale on CT correlated with hypoxia in primary non-small cell lung cancer (NSCLC, which included both extrinsic and intrinsic histopathologic markers of hypoxia: pimonidazole and Glut-1) and colorectal cancer (which included hypoxia-inducible factor 1alpha, carbonic anhydrase IX, Glut-1)[38,39]. Previous simulated modelling studies have shown that vascular heterogeneity is reflected in CT measurements of hepatic texture (e.g. entropy)[40]. Furthermore, in patient studies, tumour heterogeneity at medium and coarse texture scales on CT correlated with angiogenesis in primary NSCLC and colorectal cancer (CRC)[38,39]. In this CRC study, heterogeneity on CT combined with glucose uptake on PET correlated with vascular endothelial growth factor[39]. 006ab0faaa

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