logo
Skin expert warns 'most people' mistake deadly cancer for harmless bite - but there's one key difference EVERYONE should know

Skin expert warns 'most people' mistake deadly cancer for harmless bite - but there's one key difference EVERYONE should know

Daily Mail​29-04-2025

A leading skin expert has warned that far too many are mistaking potentially deadly skin cancer s for harmless bug bites.
In an Instagram video viewed 300,000 times, dermatologist Dr Aleksandra Brown, said that thousands could be risking their lives by dismissing the second most common form of skin cancer — squamous cell carcinoma.
More than 25,000 people in the UK are diagnosed with the condition every year. While it is highly survivable in early stages, when spotted late it can spread to other areas of the body, making it more difficult to treat.
And thousands do not know the vital signs according to Dr Brown.
'Most often patients come in thinking that they have a cyst or a little thorn or it was just a little bug bite that got tender,' said Dr Brown, who is based in Virginia in the US.
'If you have a tender spot on a sun-exposed site that has not gone away in two weeks then it is not a cyst, it is not a thorn, it is not a spider bite.
'It is probably a squamous cell carcinoma. Please see a dermatologist and have it biopsied.'
Dr Brown also urged the public to take preventative steps to avoid the disease.
View this post on Instagram
A post shared by Dr. Aleksandra Brown (@draleksandrabrown)
'You can prevent these by wearing sunscreen on sun-exposed sites,' she said.
'Sometimes this can be hard, if you work outside, you can wear SPF sleeves which are easier than reapplying sunscreen throughout the day.'
Squamous cell carcinoma is a non melanoma skin cancer. The main difference between both is the type of cell in which they develop and the pace at which they develop.
Melanoma tends to spread faster in your body than non-melanoma.
Non melanoma skin cancer accounts for 20 per cent of all cancers and 90 per cent of all skin cancers.
Experts warn that squamous cell carcinoma can vary in appearance.
The British Association of Dermatologists say that most look scaly or crusty, raised and rough as they originate from the outer layer of the skin. Underneath the scale, there may be an ulcer that bleeds easily, although this is not always the case.
The body adds that the lesion can also be sore or tender.
The carcinoma can occur on any part of the skin, but they are more common on sun exposed sites such as the head, ears, lip, neck and back of the hands.
The British Skin Foundation warns that some are more at risk than others.
For instance, those who are immunosuppressed—either due to medical treatment or conditions like HIV—as well as people who are fair skinned and more susceptible to sunburn are more likely to be diagnosed.
In order to combat the risk of skin cancer, the NHS recommends that Britons wear sunscreen when spending time in the sun, regardless of the temperature.
The health service also recommends, during spring and summer, that people spend time in the shade between 11am and 3pm, when the sun is at its strongest.
Another recommendation is to wear suitable protective clothing such as a brimmed hat and a long-sleeved top.
Studies show that when caught early the five year survival rate for cancer is 99 per cent.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Job losses at Totally as urgent NHS call firm collapses
Job losses at Totally as urgent NHS call firm collapses

BBC News

time2 hours ago

  • BBC News

Job losses at Totally as urgent NHS call firm collapses

A healthcare firm, which provided urgent care services in NHS 111 call centres, has gone into administration with the loss of 100 which employed 1,400 people across several sites in the UK, including Stockton-on-Tees and Newcastle, said workers had lost their jobs across the group but did not confirm how many had been affected at each company has been sold to PHL Group, another healthcare provider to the NHS - with the immediate transfer of 600 of its Vance, joint administrator at EY-Parthenon, said he was pleased that hundreds of jobs and "critical frontline NHS services" had been safeguarded by the sale. Derby-based Totally had been struggling since losing the NHS 111 support contract in February. Mr Vance said: "We are pleased to have agreed the sale of Totally plc which safeguards critical frontline NHS services and includes the retention of over 600 jobs." Follow BBC North East on X, Facebook, Nextdoor and Instagram.

My painful restless legs are stopping me from relaxing & nothing seems to work – I'm desperate for help
My painful restless legs are stopping me from relaxing & nothing seems to work – I'm desperate for help

The Sun

time2 hours ago

  • The Sun

My painful restless legs are stopping me from relaxing & nothing seems to work – I'm desperate for help

WE are often drawn to supplements to 'fix our health'. But, unless we are deficient in certain nutrients, then lifestyle changes are more likely to bring about noticeable changes. Most of us should get all the nutrients we need from eating a balanced diet. But we sometimes need a little extra help. For example, vegetarians and especially vegans should consider supplementing with vitamin B12, and possibly calcium, iron and zinc. Irritable bowel syndrome patients might find a probiotic is helpful to alleviate symptoms, and people with sleep issues may want to try magnesium. The only supplement the NHS recommends for all adults is vitamin D, which our bodies create in response to sufficient sunlight. The advice is to take it between October and April, but some people are advised to take it all year round, including people who have dark skin and those who are not often outdoors, for example, if they are in a care home. Here's a selection of what readers have asked this week. Q) AS soon as I relax in bed, I get a crawling sensation under my skin in my legs. Lately, it seems to be getting worse, affecting my arms. I am an 82-year-old lady and have suffered from restless legs syndrome for many years. My GP first prescribed pramipexole, which didn't help, then ropinirole, which doesn't work on its own, so I have to take co-codamol. Cardiologist explains when chest pains aren't a heart attack I worry I will have to take these for the rest of my life. My doctor won't increase the ropinirole because of the side-effects. I've been told there is nothing else that can be done. I have tried exercising, a warm bath, a massage, but nothing helps. A) Restless legs syndrome (RLS) is a neurological disorder characterised by an irresistible urge to move the limbs accompanied by uncomfortable sensations. While it most commonly affects only the legs, the arms are occasionally affected, too. Symptoms tend to be worse at night and this often affects sleep. It's not understood why people get it and there's no known cure unless it's linked to an underlying, reversible condition. Iron deficiency or low iron levels can cause it, so it's worth your GP checking these if they haven't already. It can also be caused by certain medications, including some anti-nausea drugs, antidepressants, antipsychotics and antihistamines – so again, if you take any other meds, it's worth checking if there could be a link. Ropinirole used to be recommended as a first-line treatment, but the guidelines have changed and now gabapentin (and similar drugs) are advised. Some people are unable to take this due to potential interactions. Some people have side-effects, especially older adults. So your GP might have opted away from this, but it is worth asking them. You can always download the NICE guidelines yourself or attach the link in an e-consult request for them to consider. Just search 'NICE' and 'restless legs syndrome' and you'll reach the right webpage. It may also help if you reduce caffeine and alcohol, don't smoke, sleep well and be physically active. To relieve an attack, relaxation, stretching, walking or massage can help. RLS-UK ( has useful advice and resources. My doctor said it was pointless having an X-ray, but I have had corticosteroid injections, which did nothing to ease the pain. 3 I am a 63-year-old type 2 diabetic, and I have also been having physiotherapy, which has noticeably improved my range of movement. My physiotherapist is not entirely convinced that it IS a frozen shoulder, though, and has suggested it could potentially be a form of arthritis or another condition. He has written to my doctor recommending that X-rays be carried out. I have started experiencing upper back pain, too. I am unsure whether this is connected. How do I approach my doctor on this? A) Frozen shoulder (adhesive capsulitis) is a condition that causes pain, stiffness and reduced range of movement of the shoulder joint. The symptoms are caused by the formation of adhesive or scar tissue in the joint. Studies indicate that people with diabetes may be two to four times more likely to develop frozen shoulder. Diagnosis is clinical, meaning it is based on the symptoms and examination findings rather than X-rays or scans. The main diagnostic test is whether you can do passive external rotation of the shoulder. This means that the doctor supports the patient's arm in a bent position (imagine holding a kettle) and tries to move the arm to the side. Inability to do this movement is highly suggestive of frozen shoulder. If an X-ray is obtained, it should demonstrate a normal shoulder joint. Most patients get physiotherapy, which can be supplemented by steroid joint injections. It usually resolves on its own over a year or two, although some individuals may experience longer recovery times. Physios see frozen shoulder quite frequently, so if yours is experienced and believes that other causes should be considered, then your GP is likely to take that advice. Rotator cuff injuries, bursitis, osteoarthritis and shoulder impingement are examples of conditions that can be mistaken for frozen shoulder due to overlapping symptoms. 'My body has become my enemy' Q) I AM a 63-year-old female who has always been healthy and active until having a mobility issue with my right leg for the last 13 years. It has led to foot drop. It is easy to trip and fall. It was suggested I must have had a one-off viral attack which damaged an area of my spinal cord. 3 I am so angry and frustrated. This has taken a huge toll on me mentally, and my body has responded by going into overdrive. I am overwhelmed with tiredness, but cannot sleep, and have no appetite. I am unable to relax. My body has become my enemy. Please could you advise, before I collapse? A) It sounds like the 'fight or flight' part of your nervous system may be in overdrive and also that you have a lot of negative thoughts and emotions surrounding what has happened to your body. This statement, 'my body has become my enemy', is a clue that you are most likely to benefit from cognitive behavioural therapy (CBT), which is available on the NHS. CBT could help you rebuild the relationship with your body. Please don't delay – self-refer on the NHS talking therapies webpage, or explore insurance or private options if these are available to you. Regarding the foot drop, in addition to physio and orthotics (which help prevent tripping and dragging of the toes), you should ask about whether electrical nerve stimulation would be an option for you. A device sends small electrical impulses to stimulate nerves that lift the foot and is sometimes used if the foot drop is caused by damage to the brain or spinal cord (eg from stroke or MS – multiple sclerosis). Research is ongoing into using stem cells or nerve growth factors to regenerate damaged nerves that cause foot drop. See if any trials are recruiting by asking your specialist team, exploring the NIHR Be Part of Research webpage, or by visiting

News of Scottish Government funding of £22 million to reduce NHS Lothian waiting times is welcomed
News of Scottish Government funding of £22 million to reduce NHS Lothian waiting times is welcomed

Daily Record

time2 hours ago

  • Daily Record

News of Scottish Government funding of £22 million to reduce NHS Lothian waiting times is welcomed

'This will allow for quicker diagnoses, more procedures, and better outcomes' An announcement of targeted funding to reduce NHS waiting times in Lothian has been welcomed by Fiona Hyslop MSP. The SNP parliamentarian for the Linlithgow constituency reacted to the Scottish Government's announcement of £22 million to help NHS Lothian to reduce waiting times, as part of a £106 million investment in NHS Scotland. ‌ The funding, from the Scottish Government, will focus on the longest waits for essential procedures and appointments and includes; £25 million for orthopaedics, £21 million for imaging services, £14 million for cancer treatment and £12 million for ophthalmology. ‌ Fiona Hyslop MSP said: 'The Scottish Government recognise that supporting our NHS is a key priority for people across West Lothian and this is clear from this £106 million funding boost to NHS services across Scotland. 'Across NHS Lothian, there will be an investment of over £22 million which will be key in reducing waiting times for essential procedures and appointments. 'By focussing funding on the areas where it is needed most such as, orthopaedics, cancer and diagnostics, delays can be tackled and this will allow for quicker diagnoses, more procedures, and better outcomes for people across West Lothian.'

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store