
Don't miss the signs: Doctors warn of brain tumor surge among children
"Although brain tumors are more common in adults, even younger kids can be affected by this condition. According to the National Brain Tumor Society, approximately 5.7% of all primary brain tumors occur in children and adolescents aged 0-19 years. These tumors may be benign or malignant, but either way, timely medical care is vital," says Dr. Anurag Saxena, neurosurgeon at Manipal Hospital.The symptoms of brain tumors in children can often mimic more common conditions, leading to delays in diagnosis.Dr. Saxena explains that in infants, abnormal skull growth may be an early sign, while older children may show symptoms like seizures, excessive crying, unresponsiveness, or vision issues.For teenagers, persistent headaches, dizziness, vomiting, or coordination problems can indicate the presence of a tumor.advertisementEarly diagnosis is especially critical in children, as their developing brains are more vulnerable to damage. Diagnostic imaging such as MRI or CT scans remains the cornerstone of identifying these tumors.'Sometimes, benign tumors can be removed completely through surgery. But to avoid long-term damage, it's essential to catch these conditions early,' added Dr. Saxena.The pattern is not restricted to children alone. An increasing number of young adults, especially those aged 20 to 40, are also being diagnosed with brain tumors, a shift that medical experts are calling "alarming.""Brain tumors have historically been viewed as a problem primarily affecting older adults,' says Dr. Varindera Paul Singh, neurosurgeon at Medanta. 'However, data and clinical evidence now indicate an alarming increase in brain tumors among individuals aged 20 to 40. This shift calls for a renewed approach to brain health awareness within the younger population.'Dr. Singh points out that while improved imaging technologies like MRI have led to better detection rates, they alone cannot explain the rising numbers.Environmental factors, lifestyle-related stress, and genetic predispositions are also believed to contribute, although more research is needed to confirm this.A key challenge, he says, is that symptoms in younger adults, such as fatigue, nausea, or mild behavioural changes, are often brushed off as stress or lifestyle-related.advertisement"Because these changes are often subtle, many young patients ignore their symptoms altogether, allowing tumors to grow unnoticed. It is crucial to educate both the public and primary care providers that brain tumors can occur at any age," says Dr. Singh.In children, too, the signs can be subtle, but should never be overlooked. Dr. Shiji Chalipat, pediatric neurologist at Ankura Hospital for Women and Children, highlights that immediate medical attention can be lifesaving.'Parents need to be proactive when it comes to their child's health. Just like adults, brain tumors are a common occurrence in children. Unfortunately, these tumors are linked to high morbidity and mortality, making early diagnosis and treatment crucial for improving quality of life," she says.Dr. Chalipat has outlined several red flags for parents to look out for:advertisementVomiting and Headaches: Persistent vomiting, especially in the morning or when coupled with headaches, could signal increased pressure inside the skull.Sensory Impairments: Difficulty with vision, hearing, or speech may indicate tumor growth depending on its location.Balance and Coordination Issues: Tumors affecting the brainstem may result in imbalance or trouble walking.Behavioural Changes: Sudden mood swings, irritability, or withdrawal should not be dismissed as mere tantrums.Seizures: Especially if they are new or unexplained, seizures are a strong warning sign and require urgent evaluation.Treatment plans often include surgery, chemotherapy, or radiation depending on the tumor's size, location, and type.'Parents play a critical role in recognising and responding to these warning signs,' advises Dr. Chalipat. 'With prompt action, we can ensure children receive the right medical and surgical care, and the best possible chance at recovery.'The growing prevalence of brain tumors in both children and young adults is a sobering reminder of the need to stay vigilant. Whether it's a toddler showing signs of imbalance or a young professional battling persistent headaches, the message from doctors is clear: don't ignore the signs.Early diagnosis can be the difference between life and death or between lasting damage and full recovery.Trending Reel

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The Hindu
13 hours ago
- The Hindu
All you need to know about: ectopic pregnancies
A recent case of pregnancy stunned doctors in Bulandhshahr, Uttar Pradesh: an MRI scan, conducted after the pregnant woman complained of vomiting and stomach pain, revealed a foetus growing in the liver, as per media reports. This extremely rare condition is known as an intrahepatic ectopic pregnancy. Additionally, as Ectopic Pregnancy Awareness Day went by last week, on August 1, a day dedicated to highlighting this condition and the experiences of those who have been affected, here is all you need to know about it. What is an ectopic pregnancy? An ectopic pregnancy occurs when the fertilised egg, instead of implanting itself in the uterus, implants outside of it, commonly in the fallopian tube. This sort of pregnancy cannot proceed normally. It could cause bleeding, and may even be life-threatening in some cases. Pregnancy begins with fertilisation of a sperm cell and and egg cell. The fertilised egg is then meant to travel down the fallopian tubes, which are tubes that connect the ovaries to the uterus, and attach itself to the lining of the uterus (womb). In an ectopic pregnancy, the fertilised egg attaches itself to a structure other than the uterus. When it attaches to the fallopian tubes, it is called a tubal pregnancy. Rarely, the fertilised egg may attach to the ovary, abdominal cavity or cervix. Since only the uterus is meant to carry a growing embryo, these pregnancies cannot continue. Why do ectopic pregnancies occur? Ectopic pregnancies occur when the movement of the fertilised egg is blocked. This could occur due to inflammation or scarring of the fallopian tubes, damage to the fallopian tubes (due to prior surgeries or infections), or an irregularly-shaped fallopian tube. Risk factors for ectopic pregnancy include: a prior ectopic pregnancy, having had certain sexually transmitted infections, surgery of fallopian tubes, a history of smoking, infertility and fertility treatments, endometriosis, and having an intrauterine device in place at the time of conception. Advanced age (over 35) is also a risk factor. However not all women will have any or all of the risk factors. How common are ectopic pregnancies? A 2023 research paper, Clinical Profile, Risk Factors and Outcomes of Ectopic Pregnancy in a Tertiary Care Hospital: A Prospective Indian Study published in Cureus, noted that the incidence of ectopic pregnancies in India has been reported in the range of 0.91-2.3%. The study found that amenorrhea (absence of menstruation) was the most common symptom seen in the cases it analysed. On ultrasound, the most common finding was tubo-ovarian mass. In the majority of patients studied, the ampullary region in the fallopian tube was the site of the ectopic pregnancy. According to the 'Global burden of ectopic pregnancy from 1990 to 2019: A tendency, forecasted trend and inequality analyses based on the Global Burden of Disease Study 2019', in the European Journal of Obstetrics and Gynaecology and Reproductive Biology, in June 2025, the number of ectopic pregnancies has fallen from 1990 to 2019. The study however highlights the significant burden of ectopic pregnancies, especially for low socio-demographic index countries. Addressing health inequality is crucial for developing effective intervention policies to improve global maternal health outcomes, it notes. What are the signs and symptoms of an ectopic pregnancy? Ectopic pregnancies don't always cause symptoms. Some symptoms may also be similar to those in early pregnancy such as a missed period, nausea and tenderness of breasts. Other symptoms may become noticeable later and may include: vaginal bleeding, pain in the lower abdomen, as well as pelvic and back pain, dizziness, pain in the shoulder, discomfort during bowel movements, and low blood pressure. The rupture of the fallopian tube, with sudden, sharp, abdominal pain and extreme light-headedness is a medical emergency as it can cause severe, internal bleeding. Immediate medical attention is required as it can be life-threatening. How is an ectopic pregnancy managed and treated? Many women may not know that their pregnancy is ectopic until they see a healthcare provider. Urine, blood tests and ultrasounds may be required for the doctor to arrive at a diagnosis. They are generally diagnosed early in the pregnancy. Since a pregnancy cannot proceed outside the uterus, an ectopic pregnancy is usually treated with medication or surgery. A common medication used is methotrexate: this stops the cells of the fertilised egg from growing and helps dissolve existing cells. This medication cannot be taken if the fallopian tubes are ruptured. It is important to have a confirmed diagnoses prior to taking the medication. After the medication is taken, follow-ups are required to monitor blood hCG levels (detection of pregnancy) and to determine if more medication is needed. In some cases, surgery may be required. Laparoscopic (keyhole) surgery is generally performed. The surgery may involve removing the egg from the fallopian, or removing both the egg and the tube. This depends on the amount of bleeding incurred, damage to the tube and other factors. In case of a ruptured tube, emergency surgery may be required. What happens after an ectopic pregnancy? Losing a pregnancy can be very difficult, and feelings of loss can last for a long time. It is important to seek help if required. Consulting a healthcare provider about future pregnancies is recommended. There is a higher risk for another ectopic pregnancy after having had one; however most women can go on to have successful pregnancies.


News18
19 hours ago
- News18
After 4 Years Of Suffering, Woman Discovers Sponge Left Inside Her Post C-Section
This condition is known as gossypiboma, a term used when surgical material, like a sponge, is accidentally left inside a patient. A 38-year-old woman in Delhi went through years of unexplained pain following a cesarean delivery she had undergone abroad. What seemed like routine post-surgical discomfort eventually turned into something far more serious and unexpected. According to a report in Live Science, she had given birth via emergency C-section and soon after started experiencing pain in the lower right side of her abdomen. As per the report, doctors at the time assured her it was normal post-op pain. But over time, a lump developed, and the pain became more severe. A Growing Lump It wasn't until four years later, in 2014, that the woman sought further medical advice in Delhi. Doctors carried out an ultrasound and a CT scan, which revealed a cyst in the area where she experienced pain. Initially, they suspected it to be a mesenteric cyst, a type of benign tumour that can cause discomfort and pain. But to confirm this, doctors turned to an MRI scan. This is where things got even more puzzling. According to the report, the scan showed what looked like a thick membrane inside the cyst. The image raised the possibility of a tapeworm infection, which can happen if someone consumes food contaminated with tapeworm eggs. Since imaging tests could not clearly identify what was inside the cyst, doctors decided to surgically remove it. During the operation, they found that the mass had fused with a part of the small intestine, which they had to cut and remove as well. The woman recovered well and was discharged a week later. A Sponge Caused It All The cyst was unusually large, as it was around 20 centimetres in length. But when doctors opened it up, they found a surgical sponge at the core. They believed that it had been accidentally left behind during her C-section abroad. As per the report, if the body sees any foreign object, it is treated as a threat. But since the sponge 'could not easily disintegrate," likely because it was sterile, the immune system responded by safely sealing it off inside a protective cyst instead of triggering an infection. Rare Condition This condition is known as gossypiboma, a term used when surgical material, like a sponge, is unintentionally left inside a patient. While rare, it does happen. The report mentioned that such incidents occur in about 1 in every 1,000 to 1,500 surgeries, especially in emergency situations or when surgical teams change mid-procedure. Sponges used in surgeries are meant to absorb blood, but once soaked, they can blend in with body tissue. In this case, the sponge material wasn't detectable on standard scans which made diagnosis even harder. A Call For Stricter Protocols The case report, published on July 16 by Live Science, pointed to the importance of stronger surgical protocols. It is noted that using only radio-detectable sponges and ensuring a complete count of sponges before and after procedures can help prevent such incidents. view comments First Published: Disclaimer: Comments reflect users' views, not News18's. Please keep discussions respectful and constructive. Abusive, defamatory, or illegal comments will be removed. News18 may disable any comment at its discretion. By posting, you agree to our Terms of Use and Privacy Policy.


Time of India
20 hours ago
- Time of India
How a suspected flu led to a brain tumour diagnosis for a 26-year-old man: Don't ignore headaches, fatigue, and other warning signs
What began as a simple case of suspected flu turned into a life-altering diagnosis for 26-year-old triathlete Kieran Shingler from Warrington, England. Initially experiencing what seemed like routine cold symptoms: a sore throat, runny nose, and persistent headache where Kieran believed he had seasonal flu or Covid-19. However, within weeks, his health rapidly deteriorated, leading to shocking medical discoveries. Doctors revealed he had an aggressive Grade 3 astrocytoma, a fast-growing malignant brain tumour, and gave him just one year to live. His journey highlights how easily life-threatening conditions can mimic common illnesses, delaying treatment. How brain tumour symptoms mistaken for flu and covid-19 On Bonfire Night 2022, Kieran experienced mild symptoms: a sore throat, a runny nose, and a nagging headache. Like millions during that period, he suspected Covid-19 and tested himself multiple times. When all tests came back negative, he and his girlfriend, Abbie Henstock, assumed it was the flu. But this 'flu' never went away. As reported, in the weeks that followed, Kieran's condition deteriorated rapidly. He became fatigued, struggled to keep food down, and developed excruciating headaches—pain that was unusual even for flu or migraines. Surprisingly easy ways to protect your brain and prevent stroke 'He was so fit—doing triathlons, working out almost every day—and then he suddenly couldn't even eat without being sick. We knew something was seriously wrong,' Abbie recalled. Two weeks after his symptoms started, Kieran's late mother, Lisa, noticed how badly he was struggling and contacted their family GP. Concerned about possible meningitis, the GP referred him to Warrington Hospital. At the hospital, doctors ran tests and performed a CT scan, which revealed a shocking discovery: there was a mass on Kieran's brain. He was immediately blue-lighted to The Walton Centre in Liverpool, a specialist neurology facility. Source: SWNS Multiple surgeries and MRI scans uncover fast-growing malignant brain tumour At The Walton Centre, an MRI scan confirmed a tumour was obstructing the flow of cerebrospinal fluid, which helps protect the brain and spinal cord. This blockage was causing dangerous intracranial pressure that could have proved fatal if not treated immediately. Doctors explained that surgery was necessary—not just to treat the tumour but also to relieve the fluid build-up in Kieran's brain. First surgery: Emergency procedure to relieve pressure Kieran underwent an Endoscopic Third Ventriculostomy (ETV), a minimally invasive surgery designed to create a new pathway for fluid circulation and reduce pressure inside the brain. Initially, the surgery worked, and Kieran began to feel better. But this was only the start of a complex medical journey, as the tumour itself still needed to be addressed. Second surgery: Removing the tumour and biopsy A few weeks later, doctors performed a craniotomy to remove as much of the tumour as safely possible and take samples for biopsy. While this surgery succeeded in reducing tumour size, it left Kieran with short-term memory loss, a common side effect when operating on critical brain regions. In December 2022, just one hour before his third surgery (to insert an external shunt after the ETV failed), doctors revealed the devastating biopsy results: Grade 3 Astrocytoma—a fast-growing, malignant brain tumour. What is a Grade 3 Astrocytoma Astrocytomas develop from astrocytes, star-shaped brain cells that support nerve function. Grade 3 tumours are: Aggressive and fast-growing, making them more difficult to treat Infiltrative, meaning they spread into nearby brain tissue Known to cause headaches, vision changes, cognitive impairment, speech issues, and seizures These tumours often require multimodal treatment—surgery followed by radiotherapy and chemotherapy—but even then, they have a high recurrence rate. Doctors explained to Kieran's family that such tumours are rarely curable and, in his case, he likely had only 12 months to live. To shield him from extra distress during the holidays, his family waited until after Christmas to tell him. 'When I was finally told, I was scared and angry. I kept asking: why me?' Kieran said. Radiotherapy brings hope as tumour reduces to 0.35 cm without ongoing treatment In January 2023, Kieran began 30 sessions of radiotherapy alongside chemotherapy at The Clatterbridge Cancer Centre. This approach aimed to kill remaining tumour cells and slow its growth. The initial results were promising. By February 2023, MRI scans revealed the tumour was shrinking—a rare moment of relief for Kieran and Abbie amid months of uncertainty and fear. Unfortunately, by mid-2023, the tumour became resistant to the treatment and began growing again. Doctors switched to lomustine chemotherapy, which successfully reduced the tumour but caused liver damage, forcing doctors to stop treatment. Surprisingly, even without active treatment, Kieran's tumour continued shrinking for 19 months, reducing from 5.5 cm to just 0.35 cm—an almost miraculous development. Brain tumour returns in 2025 as Kieran turns to fundraising and alternative therapies The respite didn't last. In June 2025, a routine MRI revealed that the tumour was growing again. After years of fighting, three surgeries, multiple rounds of radiotherapy and chemotherapy, and temporary recovery, Kieran was once again facing the grim reality of a recurring, aggressive brain cancer. Determined to turn pain into purpose, Kieran and Abbie launched Kieran's Krew, an online fundraising campaign. Initially intended to support brain cancer charities, it soon grew into a community-driven movement funding alternative therapies like: Oxygen therapy, which may improve cellular healing Red-light therapy, which some studies suggest could reduce inflammation To date, over £57,000 has been raised to support brain tumour charities and provide Kieran with therapies that improve his quality of life. 'At every scan, we hoped for good news. Even when it was shrinking, we knew it could change at any time. Now we want to use our journey to help others,' Abbie explained. The brain tumour diagnosis profoundly changed Kieran's life. Short-term memory loss, chronic pain, hospital visits, and emotional distress became part of daily life. Yet, Kieran remained determined to focus on positive moments, supported by family, friends, and the broader community that rallied around him. 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