
Pemphigoid or Psoriasis? 65-Year-Old's Remote Diagnosis Race
A 65-year-old man developed severe cutaneous toxicity, presenting as a rare bullous pemphigoid (BP) rash after 2 years on nivolumab. Notably, the reaction occurred in an outpatient setting during the COVID-19 pandemic. With coordinated support from rural providers and the use of telemedicine, his corticosteroid-refractory immune checkpoint inhibitor (ICI) toxicity was successfully managed.
The case reported by Tom Marco, DO, and colleagues from the Department of Internal Medicine, University of Arizona College of Medicine, Tucson, Arizona, highlighted how remote monitoring helped diagnose and manage a rare but serious complication of cancer therapy.
The Patient and His History
The patient with no prior medical history presented to the emergency department with gross haematuria. A CT scan of the abdomen and pelvis revealed a large right renal mass, embracing the inferior margin of the liver without renal vein involvement or capsular extension. A CT of the chest corroborated no definite metastasis to other organs or lymph nodes. Because there was no evidence of distant metastatic disease on imaging, a right radical nephrectomy with adrenalectomy was performed by urology, without complications. The pathology report was notable for clear cell renal carcinoma.
Because the patient came from a rural area, the examinations took place at a centre 3 hours away from his place of residence. The patient was subsequently examined by medical oncology, which calculated the probability of early disease progression to be low, with a recurrence rate of 8.4%. Given the low risk for recurrence, no adjuvant systemic therapy was recommended. The patient continued follow-up with medical oncology and remained under surveillance with CT scans every few months.
Findings and Diagnosis
At 24 months, a new right upper lobe (RUL) pulmonary nodule measuring 6 mm was found on chest CT. The nodule size was considered nonpathologic. Furthermore, the lesion was not feasible for biopsy, and the patient continued to be under close surveillance.
By month 36, the RUL pulmonary nodule measured 10 mm. A new left upper lobe nodule measuring 6 mm and a new right lower lobe lesion measuring 2 mm were discovered. A follow-up PET scan showed nonavid nodules, and biopsy was not feasible.
At 48 months, lesion progression prompted biopsy, which confirmed metastatic recurrence of renal cell carcinoma (RCC). The cancer was staged as IV (pT2cN0cM1).
First-line treatment with nivolumab and cabozantinib was initiated.
Cycles 2-5: The patient experienced mild fatigue, a grade 1 skin rash, gastrointestinal symptoms, and a 4 kg weight loss.
Cycle 9: Weight loss exceeding 10% of body weight prompted cabozantinib dose reduction.
Cycle 13: The patient developed diffuse skin changes, including blisters and open lesions, which led to cabozantinib discontinuation.
Cycle 14: Despite stopping the TKI, he developed severe blistering skin reactions involving more than 30% of the body surface area. ICI therapy was paused, and high-dose corticosteroids were initiated.
Skin biopsy confirmed BP, a rare autoimmune blistering disorder. The patient was treated with systemic corticosteroids, high-potency topical steroids, and doxycycline. Due to the limited response, rituximab was introduced for corticosteroid-refractory disease. After four doses, marked clinical improvement was observed: The skin lesions regressed, and no new blisters developed.
By day 172, the patient was free of skin symptoms. Given the absence of active disease and the severity of prior toxicity, a surveillance protocol was adopted.
Discussion
BP is a rare but potentially life-threatening immune-related adverse event (irAE) associated with ICI therapy. Early recognition and prompt, aggressive management, including biologic agents such as rituximab, are essential to ensure optimal outcomes.
The combination of ICI with TKI has become the standard therapeutic approach for the initial management of advanced RCC due to decreased mortality and increased long-term survival rates. Although this combination of medications has positively affected RCC treatment, the side effects can be severe.
In this case report, it was initially suspected that cabozantinib caused cutaneous manifestations and gastrointestinal adverse effects. In numerous studies, more than 70% of patients taking cabozantinib developed one or more cutaneous toxicities, including erythema, hand-foot skin reactions with or without blisters, pruritus, seborrheic dermatitis, stomatitis, and xerosis.
Alternatively, cutaneous manifestations with nivolumab have been reported in approximately 34% of patients or fewer and include maculopapular rash, eczema, lichenoid rashes, vitiligo, pruritus, and rarely, bullous eruptions.
Although the dose of cabozantinib was initially reduced and eventually stopped due to multiple suspected toxicities, the patient developed a new, rapidly progressing corticosteroid-refractory rash that continued to worsen to grade 4 toxicities. The pathology was characteristic of extremely rare BP ICI toxicity. Consequently, the decision to discontinue nivolumab therapy was made. Despite discontinuation of the offending agent, his BP began to improve only after the initiation of rituximab in combination with corticosteroids. This suggests that the cutaneous toxicity was attributable to nivolumab, indicating that it was an ICI-related adverse effect.
The mechanisms underlying irAEs are not fully understood. Multiple theories have been proposed, including a pro-inflammatory state, uncontrolled activity of T cells, enhanced immune activation and response, and cytokine release. Skin irAEs are the most common, encompassing 17%-40% of toxicities.
This case highlights the complex care challenges faced by rural patients with cancer. The patient resided more than 3 hours from the nearest specialised oncology centre, an access barrier further compounded by the COVID-19 pandemic. With less than 7% of oncologists available in rural areas, there is a significant gap in care.
The patient was able to receive cancer treatment, undergo detailed toxicity monitoring, and benefit from multidisciplinary input without a significant travel burden. Early detection and management of high-grade toxicities through remote assessments and coordinated care enabled successful treatment outcomes. Given this, structured telehealth surveillance protocols are crucial and can effectively serve rural areas that lack specialty centres.

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


The Hill
4 hours ago
- The Hill
Flu, COVID can reawaken dormant breast cancer cells: Study
Respiratory infections like COVID-19 and the flu can activate dormant cancer cells in breast cancer patients who are in remission, new research finds. The study, published in Nature, found that common viruses can reawaken small numbers of dormant breast cancer cells in the lungs. Researchers began investigating the link after the team noticed that U.K. patients who were in remission from breast cancer and tested positive for COVID later showed a two-fold increase in cancer-related deaths. They also analyzed a U.S. database that included nearly 37,000 patients and found that COVID infection was associated with a more than 40 percent increased risk of metastatic breast cancer in the lungs. Studies on mice found that influenza and COVID infections triggered dormant breast cancer cells after just days of infection. Within two weeks, researchers observed 'massive expansion' of the cancer cells into metastatic lesions by more than 100 times. Scientists have suspected that common viruses like Epstein-Barr can trigger some cancers. Human papillomavirus (HPV) is already documented to trigger cervical cancer. When it comes to breast cancer, however, research on human cells was limited, and it's not entirely known how the virus triggers the disease to spread. The findings suggest the body's immune response plays a role. After breast cancer goes into remission, a tiny number of cells remain dormant in lung, bone and liver tissue. Sometimes, inflammation can wake up the cells. In the mouse experiments, both influenza A and coronavirus only reawakened dormant cells if they triggered an inflammatory cytokine response. More research is needed to see if vaccination makes a difference when it comes to the possibility of reawakening dormant cells.


Buzz Feed
4 hours ago
- Buzz Feed
25 Ways People Won The Great Genes Lottery
Recently, I wrote an article sharing people's answers to the question, "In what small way have you won the genetic lottery?" and in response, even more people detailed their own genetic "wins." It's always fun to appreciate the positives about yourself, so I decided to share! Here are some of the best: "I don't have B.O. when I sweat, and I've read it's a genetic mutation. I don't wear deodorant, and I've gone a whole 10 days without a full shower (camping), and my pits and feet don't smell. Only one of my kids got this genetic gift, and the other kid is so bummed that they started getting B.O. at 11." —Anonymous, 48, Los Angeles, CA "I have no wisdom teeth, none. I was also born without tonsils." —Anonymous, 45, Dallas, TX "I have naturally long and curled eyelashes. They are blonde, so I have to use mascara, but I've never used an eyelash curler in my life. People assume I'm wearing falsies." "I have naturally big lips that people made fun of me for as a child, and now everyone is jealous of my naturally plump big lips. Thanks, Kardashians." —Anonymous, 28, NJ "I've had abs since I was 7. I'm female, and neither of my parents has a very athletic build, but it's very easy for me to just always have them. Even if I've gained weight in my face or body, my abs always show through." "My irises have gradually turned a gold/yellow color. They're basically a combination of several colors, and, when mixed together, they look gold. I get a lot of comments on them and people ask if I wear contacts." —C., 30s "I have never experienced a headache. It's difficult for me to even imagine what it would feel like. Once I had a full-blown migraine attack with sensory aura, nausea, and sensitivity to sounds and smells, but no headache." —Anonymous "I've got great skin! Inherited from my mom, who is in her 70s and has never had any work done, but looks like she has. Terrible spine and joint problems, though. 😒" "I'm resistant to COVID-19. Everybody in my workplace got it, and I didn't. My husband even got it, and I still didn't get it." —Anonymous "I'm lucky two different ways. I never had wisdom teeth, and I don't get caffeine headaches on days I don't have caffeine." —Anonymous, 45, IL "My mom's side of the family has a gene mutation that leads to a very aggressive form of stomach cancer that can't be caught early enough to effectively treat. Turns out, I don't have it! It's one of the gene mutations where if you don't have it, your kids won't either. Neither I nor any of my cousins have it, so we don't have to worry about it anymore!" "My hair is not graying. I'm 71 and have long blonde hair. My sister grayed at age 30." "My mother had three sisters. The oldest did not go salt and pepper gray until she was nearly 90. We all thought she was lying and dying it! But then she started going salt and pepper at nearly 90. The second oldest grayed at 50. The third grayed at 40 and the youngest grayed at 30. So it seems that somehow the oldest grays late and the youngest grays early."—Anonymous, 71, TX "My dad and I don't get hangovers. My mom, sister, and brother hate that! We do get bad reactions to bug and bee stings, but on the whole, pretty happy about my luck!" —Kristin, 53 "I don't really scar. I've had stitches more than once, along with some serious injuries. After about two years, all scars disappear." "I'm immune to jellyfish stings! I found this out by swimming through a huge school of jellyfish, and my sister got stung, but I didn't." —Anonymous, 31, MN "Mosquitoes don't seem to like me. I've had, maybe, four bites in my life (all before the age of 12, and have had none since). Kind of a weird flex, but super handy!" —Anonymous, 24 "I have freakishly good eyesight. I can read signs at 35+ feet away. I didn't realize how special that was until I had kids. One can see 20/20, but I can see way farther than him, easily. It's not even close!" "I was born without tonsils, which is chill because that, plus my immune system, means I've only ever been seriously sick twice, once with COVID and once when I got mono." —Anonymous, 37, CA "I'm not allergic to poison ivy/oak/sumac. I've been exposed to all of them often and have never gotten a reaction. I'm either very lucky, or immune, but I don't plan on testing that theory any time soon." "Not a particularly fun or sexy one, but I have naturally low blood pressure, which vastly reduces my long-term risk of stroke and heart disease." —Anonymous, 36, North Carolina "I have an extra artery supplying blood to my retina in each eye. It's called a cilioretinal artery. If the main artery is ever damaged or blocked, it can cause immediate vision loss in that eye. My vision would be protected though, because the extra artery would continue to supply blood to my retina." —Anonymous "Redhead here! I have extremely decreased pain. (Broke three bones, and each time I had no clue until an X-ray.) I helped someone move on a broken foot! Had no clue until I was limping later." "I have freakishly nimble and long toes that I can pick things up with. It's nice because I don't have to bend over to pick things up." —Anonymous, 36, MA "I inherited my dad's ability to not get hangovers, no matter what I drink!" —Anonymous, 41, TX And finally: "I inherited amazing hearing from my grandmother. Many a time, I've heard people whispering in other rooms, and shocked them by commenting on what they'd said." —Anonymous, 38 What d'you think? Do you have any of your own "genetic lottery wins" to share? Let me know in the comments! Or, if you prefer to stay anonymous, you can check out this anonymous form. Who knows — what you share could end up as part of a future BuzzFeed article! Please note: some comments have been edited for length and/or clarity.


San Francisco Chronicle
6 hours ago
- San Francisco Chronicle
Got the sniffles? Here's what to know about summer colds, COVID-19 and more
Summer heat, outdoor fun ... and cold and flu symptoms? The three may not go together in many people's minds: partly owing to common myths about germs and partly because many viruses really do have lower activity levels in the summer. But it is possible to get the sniffles — or worse — in the summer. Federal data released Friday, for example, shows COVID-19 is trending up in many parts of the country, with emergency department visits up among people of all ages. Here's what to know about summer viruses. How much are colds and flu circulating right now? The number of people seeking medical care for three key illnesses — COVID-19, flu and respiratory syncytial virus, or RSV — is currently low, according to data from the Centers for Disease Control and Prevention. Flu is trending down and RSV was steady this week. But COVID-19 is trending up in many mid-Atlantic, southeast, Southern and West Coast states. The expectation is that COVID-19 will eventually settle into a winter seasonal pattern like other coronaviruses, but the past few years have brought a late summer surge, said Dr. Dean Blumberg, chief of pediatric infectious diseases at University of California Davis Children's Hospital. Other viruses circulating this time of year include the one that causes 'hand, foot and mouth' disease — which has symptoms similar to a cold, plus sores and rashes — and norovirus, sometimes called the stomach flu. Do viruses spread less in the summer? Many viruses circulate seasonally, picking up as the weather cools in the fall and winter. So it's true that fewer people get stuffy noses and coughs in the summer — but cold weather itself does not cause colds. It's not just about seasonality. The other factor is our behavior, experts say. Nice weather means people are opening windows and gathering outside where it's harder for germs to spread. But respiratory viruses are still around. When the weather gets too hot and everyone heads inside for the air conditioning, doctors say they start seeing more sickness. In places where it gets really hot for a long time, summer can be cold season in its own right. 'I grew up on the East Coast and everybody gets sick in the winter,' said Dr. Frank LoVecchio, an emergency room doctor and Arizona State University researcher. 'A lot of people get sick in the summer here. Why is that? Because you spend more time indoors.' Should you get another COVID-19 booster now? For people who are otherwise healthy, timing is a key consideration to getting any vaccine. You want to get it a few weeks before that big trip or wedding, if that's the reason for getting boosted, doctors say. But, for most people, it may be worth waiting until the fall in anticipation of winter cases of COVID-19 really tick up. 'You want to be fully protected at the time that it's most important for you,' said Dr. Costi Sifri, of the University of Virginia Health System. People at higher risk of complications should always talk with their doctor about what is best for them, Sifri added. Older adults and those with weak immune systems may need more boosters than others, he said. Are more younger kids getting sick with COVID-19? Last week, the CDC noted emergency room visits among children younger than 4 were rising. That makes sense, Blumberg said, because many young kids are getting it for the first time or are unvaccinated. Health Secretary Robert F. Kennedy Jr. said in May that the shots would no longer be recommended for healthy kids, a decision that health experts have said lacks scientific basis. The American Academy of Pediatrics still endorses COVID-19 shots for children older than 6 months. How else can I lower my risk? The same things that help prevent colds, flu and COVID any other time of the year work in the summer, doctors say. Spend time outside when you can, wash your hands, wear a mask. And if you're sick, stay home. ___ The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute's Department of Science Education and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.