Juvenile Bunion Deformities

Juvenile Bunion Deformities

This article was recently published in the Pediatric Society of Greater Dallas newsletter. Committed to improving orthopedics care of pediatric patients in all settings, Scottish Rite for Children specialists are regular contributors to this publication for local pediatricians.

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What are Juvenile Bunions?
Juvenile bunions, a deformity of the foot, are a common cause of frustration for patients, their parents and medical providers. Fortunately, the vast majority of bunion deformities in children and adolescents are asymptomatic and therefore require no intervention aside from parental reassurance. For those deformities that cause difficulty with shoe wear and pain refractory to conservative treatment modalities, surgical correction is a reasonable option. It cannot be overstated, however, that appropriate surgical management mandates an in-depth understanding of the component deformities to avoid the historically high rate of recurrence and failure following operative treatment.

How Do Adult Juvenile Bunions Differ From Adult Bunions?
Clinically, adult and juvenile bunions appear very similar with lateral deviation of the great toe and a medial eminence at the metatarsophalangeal (MTP) joint resulting from uncoverage of the medial metatarsal head. These are, however, very different deformities. Adult bunions are
most commonly acquired deformities from tight shoe wear which leads to attenuation of the medial sided soft tissues at the MTP joint, lateral deviation of the hallux and usually pronation of the toe as well.

What Causes Bunions?
The cause of juvenile bunions is neither completely understood nor agreed upon. Hypermobility of the first ray, an associated flatfoot and obliquity of the lateral cuneiform have all been postulated as causative factors. However, the deformity is most likely congenital and results from external orientation of the articular surface of the metatarsal head.

How Do Bunions Appear in Radiographs?

Radiographically, both adult and juvenile bunions are characterized by angulation between the first metatarsal and the proximal phalanx (hallux valgus angle or HVA) as well as an increase in the angle subtended by the axes of the first and second metatarsals (intermetatarsal angle or IMA). The distinguishing characteristic of the juvenile deformity is a more lateral orientation of the distal metatarsal articular surface. Whereas in adult bunions, the articular surface is usually perpendicular to the metatarsal shaft. In younger patients, the angle between the shaft and the articular surface (distal metatarsal articular angle or DMAA) is elevated. This results in lateral deviation of the toe with maintained congruency of the MTP joint. In contrast, adult bunions usually demonstrate varying degrees of joint incongruency between the base of the proximal phalanx and the metatarsal head.

Can Bunions Be Prevented?
Because juvenile bunions are congenitally acquired, there are no means by which the deformity can be prevented. Moreover, once noticed, no well-accepted means of stopping deformity progression are available. Commercially available toe spacers, bunion straps and physical therapy cannot alter the abnormal anatomy of the distal metatarsal articular surface and therefore have no role in the management of this clinical entity. Straps and spacers that force the great toe more medially and the give the outward appearance of a straighter hallux do so by creating incongruity at the MTP joint which can alter range of motion and oftentimes cause discomfort.

What Shoes and Pads Help with Juvenile Bunions?
As mentioned above, in the absence of pain or difficulty with shoe wear, parental reassurance is the best course of action. In the presence of symptomatic deformities, nonoperative measures are all that is usually required to keep children active and happy. Shoe wear modifications are the simplest and oftentimes most effective course of action. Adolescents and their parents should be encouraged to find a well cushioned stability shoe with a wide toe box and flexible uppers. For those children required to wear leather shoes, boots or cleats due to school uniform requirements or recreational desires, most cobblers can create extra space in the region of the medial eminence using a “ball and ring” shoe stretcher. Should shoe modifications fail to provide complete relief, silicone bunion pads placed over the medial eminence can also be helpful. In children with flexible flatfoot deformities and symptomatic bunions, using a soft shoe insert to elevate the medial half of the heel and support the arch can offload any plantar-medial pressure by elevating the medial column of the foot.

Is Surgery Necessary for Bunions?
When prolonged conservative treatments fail to provide relief, surgical intervention is a reasonable option. Though recommendations vary with regard to the timing of surgery, due to historically poor results following the surgical treatment of juvenile bunions, many advocate to delay surgery until adolescents are within one or two years of skeletal maturity.

Females typically reach skeletal maturity at age 14 while males reach skeletal maturity at age 16. Better understanding of the congenital nature of the juvenile bunion and the importance of correcting the DMAA during operative treatment will likely lead to a dramatic reduction in recurrence and surgical failure, ultimately driving down the age at which operative intervention can be successfully undertaken.

Who is Qualified to Perform Surgery to Correct Juvenile Bunions?
As such, surgery should be performed only by those with a clear understanding of this specific deformity such as a fellowship-trained pediatric orthopedic surgeon or a fellowship-trained orthopedic foot and ankle specialist who is comfortable caring for pediatric patients.

Anthony I. Riccio, M.D., is a pediatric orthopedic surgeon caring for children and adolescents at Scottish Rite for Children. He is the director for the Center for Excellence for Foot.

Share Your Story: A Visit From the Tooth Fairy

Share Your Story: A Visit From the Tooth Fairy

Meet Jade, a patient who is treated by our experts in the Center for Excellence in Foot. Learn more about her journey below.

Blog written by Jade’s mom, Deirdra, of South Carolina. 

We first noticed a growth on Jade’s ankle in March 2017. Initially, we went to her pediatrician and were told that it was cancer. They did an X-ray and the doctor could not determine what the growth was. He then sent us to Scottish Rite for Children and as soon as we met with Dr. McIntosh we all felt better

Jade needed a CT scan to take a better look at her ankle. Luckily, we learned that she in fact did NOT have cancer. Jade has an incredibly rare condition called Trevor’s Disease. Basically, this causes an overgrowth of cartilage and we were told to come back in six months to check for additional growth.

In October 2017, Jade started to experience pain when walking and running. It also happened to be time for her follow-up appointment, so after discussion with Dr. McIntosh, we determined that surgery would be the best option for Jade. Her surgery was scheduled for the next month. It was the day of her surgery and everyone was amazing – the nursing staff, the doctors and even the pastor who prayed with us made us feel at ease. Jade did wonderful and even woke up a few dollars richer. She had a couple of loose teeth that the anesthesiologist needed to remove, and the tooth fairy visited her in the operating room! It was incredibly special for us to have such a caring staff.

At the time of her surgery, we were living in Texas. We have since moved to South Carolina, but we still make annual trips back to Dallas just to see Dr. McIntosh for Jade’s follow-up appointments. Scottish Rite for Children means everything to us. Everyone is willing to help, and they make all children feel special. When a kiddo is going through major surgery, it is so nice to have amazing staff surround you for every step of the journey.

DO YOU HAVE A STORY? WE WANT TO HEAR IT! SHARE YOUR STORY WITH US.

Get to Know our SRH Staff: Carrie Wilson, Ambulatory Care

Get to Know our SRH Staff: Carrie Wilson, Ambulatory Care

What is your role at the hospital? 

I am the RN coordinator for Dr. Richards and I also assist with Dr. Sucato’s scoliosis clinic. My primary role is providing education to patients and families, as well as helping to get patients ready for surgery to make sure medical clearances are obtained. One day to the next is never the same!

What do you enjoy most about Scottish Rite for Children?
The patients and their families!

What was your first job? What path did you take to get here? How long have you worked here?
My very first job was as a lifeguard when I was in high school. During college, I had several different jobs. I worked at a restaurant in the summers (where I met my husband to be), I worked for a stockbroker and I worked at Dillard’s.

I started at the hospital during my last semester at Texas Woman’s University. I was initially a nurse tech and then after I graduated, I was hired as a full-time inpatient nurse. As of this month, I have worked here for 32 years and I’ve been the RN coordinator for Dr. Richards for the past 22 years.

What are you currently watching on Netflix?

Call the Midwife
Who would you most like to swap places with for a day?

Jerry Jones (owner of the Dallas Cowboys) – although I don’t think he could handle my job if we had to “swap”!
What is a fun or interesting fact about your hometown?My hometown is Des Plaines, Illinois. It is the home of the first McDonald’s franchise.
What is your favorite thing to do when you’re not working?
Watching football and spending time with my family.

Share Your Story: Parker and the Superhero Leg

Share Your Story: Parker and the Superhero Leg

Meet Parker, a patient who is treated in our Prosthetics and Orthotics department. Learn more about his journey below.

Blog written by Parker’s father, James, of Flower Mound. 

In August 2012, our family traveled to Nanchang, China to adopt our two youngest sons, Parker and Xander. Overnight, our family of four expanded to six and we were fortunate to be blessed with two of the sweetest, most resilient boys you will ever meet. As you can imagine, it was a life-changing event that we will never forget.

Prior to our journey to China, we were connected with Texas Scottish Rite Hospital for Children as we prepared for Parker and Xander’s arrival here in the U.S. Both boys were born with limb differences and we knew that we would need to find a health care provider that could handle their special needs. In Parker’s case, we were particularly curious to learn what options were available for him, since he was born without his right femur and tibia. He was unable to walk in the traditional sense.

From our very first consultation onwards, the Scottish Rite Hospital staff could not have been more accommodating – from walking us through how the care process would work to answering our questions about artificial limbs. Over the years, we had heard many glowing stories from friends and acquaintances describing what the hospital meant to them and their families, but none of this really hit home until we got to experience all this for ourselves.

Once we arrived back home to the U.S., Parker was pretty overwhelmed with all the changes. At only 20 months, he had already been whisked away from the only home he knew, an orphanage in Nanchang. Everything and everyone he had ever known was gone and he was then inserted into a crazy family, which consisted of a new Mom and Dad, two older siblings and a younger sibling that was going through a similar adjustment period. Add into the mix a couple of large Great Danes and you basically have a recipe for constant chaos around the Wood house.

Although he was (and still is) amazingly resilient, it was a huge adjustment. While in China, he began to learn a few words in Mandarin and now he was challenged with learning a new language. Communication was difficult and further exasperated by all the complex emotions he was feeling. He was very shy, uneasy in public and struggled a lot with separation anxiety.

During this period, Parker had his first visits to our local pediatrician and, while she is fantastic, he was absolutely terrified – you could literally feel the heat waves coming off his body. We feared the worst when the time came to start our visits at Scottish Rite Hospital. Since he had been born with a partial foot, the process was difficult and would not be as easy as just fitting him for a prosthesis. In order to make things work, he would need to have his partial foot removed or work around it. This was not an easy decision for us since he used that partial foot to pseudo-walk on his knee.

When the time came for the surgery, we really didn’t know what to expect. Parker’s visits to the hospital were successful and he had already taken pretty well to Dr. Herring and “Dr. Kara.” Surgery and overnight visits were something we honestly weren’t sure he was prepared for emotionally

What actually transpired was beyond any of our expectations.

From the moment he arrived, we were greeted with countless friendly faces in his room. For a kid who normally hated large crowds, he really ate it all up. It’s hard to imagine having a fun time during major surgery, but I daresay he did – at least as much as you can when having your foot amputated. Probably the best thing we can say about Scottish Rite Hospital is that they took a really scary event in his young life and turned it into a positive memory. After the surgery, he was made to feel like a celebrity, and he left a different kid in so many ways.

patient being diagnosed
patient with a robot behind him

The entire experience was truly remarkable.

In the years that have followed, Scottish Rite Hospital has become a routine part of Parker’s life. I’ve never met a kid that’s more excited to go to the doctor and he loves to point out the hospital when we drive by. Seeing him walk for the first time was miraculous and we’ll never forget the smile on his face when he discovered how to walk on his own. He’s been the talk of the playground at school – but in a good way. We hear kids all the time telling their parents that they “wish they could have a cool leg like that” or “Mom! Look! That kid has a Transformer leg!” That’s not to say that it’s all been sunshine and roses of course, but it helps. Getting to meet other kids with similar limb differences and being able to see firsthand how others have been able to use their prosthetic legs to run and dance has made it so much easier for him to just be a kid and have a normal life. 

Parker is a confident kid who now has the ability to get out there and try activities that his siblings have enjoyed. He has tried gymnastics, soccer, t-ball and is about to give basketball a whirl. He may not always have the speed that other kids have, but he is able to get out there, compete and surprise kids with his craftiness. It’s pretty incredible to watch.

As parents, we’re eternally grateful for all the wonderful work that Scottish Rite Hospital has done, not only for our own children, but also for countless children throughout the U.S. and beyond. It’s a truly magical place.

Parker’s Superhero Leg from Scottish Rite for Children on Vimeo.

DO YOU HAVE A STORY? WE WANT TO HEAR IT! SHARE YOUR STORY WITH US.

Share Your Story: Pursuing My Dreams

Share Your Story: Pursuing My Dreams

Meet Jasmine, a patient in our complex adolescent foot and ankle clinic. Learn more about her journey below.

Blog written by Jasmine, age 17 of Garland.

jasmine on wheelchair

Hi everyone! I’m Jasmine, a patient at Texas Scottish Rite Hospital for Children in the complex adolescent foot and ankle clinic. My journey started around August 2013, when I began to notice an aching pain in my left foot. As an athlete, I never thought anything of the pain, other than just soreness. As the pain progressed, my parents decided to take me to an orthopedic surgeon. After several visits with the doctor, which resulted without a diagnosis, plus the idea that I was “just imagining the pain,” I gave up hope in finding relief.

In July 2016, at my annual physical, my parents mentioned that I was still experiencing agonizing foot pain. My doctor then referred me to Scottish Rite Hospital, with the hope of finding some answers. As a patient who had previously had my concerns dismissed, I was terrified of hospitals and doctors. My first appointment was with Dr. Podeszwa, where I was diagnosed with bilateral flat feet and accessory navicular. Flat feet is a condition where the arches of my foot were collapsed and accessory navicular is where I have an extra bone on the inside of my foot. Dr.Podeszwa sent me to be fitted for custom orthotics and also referred me to the complex adolescent foot and ankle clinic with Dr. Riccio and Dr. Zide.

I wore the custom orthotics for a while, but they were not successful and at this point it looked like surgery was my next option. During this time, other aspects of my life were changing due to the constant pain I was experiencing. I stopped hanging out with friends because I was always thinking about my foot pain. Also, the thought of quitting taekwondo, a sport I loved, was becoming more and more present.

Dr. Riccio and Dr. Zide came up with a plan to remove my accessory navicular and reconstruct my foot to form an arch. I had my first surgery on my left foot in March 2017. After the surgery, I stayed in the hospital overnight and was discharged the next day. I was in a splint for two weeks, a cast for six weeks, a boot for four weeks and before I knew it, was walking with normal shoes. Like any surgery, recovery is far from easy, but thanks to the wonderful care I received at Scottish Rite Hospital, it was so much better.

In June of 2018, I had the exact same surgical reconstruction performed on my right foot. Since I had already undergone this same surgery on my left foot, the second surgery was a breeze. My recovery on my right foot was picturesque. It was as easy and simple as recovering from surgery could be. Currently, I am five months post-op from my second surgery and I can say that I am feeling great!

MY NUMBER ONE PIECE OF ADVICE IS TO STAY POSITIVE! ALWAYS KNOW THAT YOU CAN GET THROUGH ANYTHING AND THAT YOU DON’T HAVE TO DO IT ALONE.

Everyone is rooting for you to have a successful and smooth road towards recovery, including your family, friends and especially the people at the hospital. Recovery isn’t always easy, but the end result will always be worth it! My surgery gave me back my life. Because of Dr. Riccio, Dr. Zide and their staff, I can do whatever I want without having to worry about pain!

jasmine outside the hospital

Scottish Rite Hospital means hope and happiness to me. Because of my experience here, I want to become an orthopedic surgeon. My dream is to give patients hope and “give children back their childhood,” just like Dr. Riccio and Dr. Zide have done for me.

I also had the opportunity to participate in the Perry Initiative Program, which gave me the opportunity to take a closer look into orthopedics. Through this program, I was able to meet Dr. McIntosh. She has encouraged me to pursue my dream of becoming an orthopedic surgeon.  I have been able to shadow Dr. McIntosh, Dr.Riccio and Dr.Zide in each of their clinics.

I MAY ONLY BE 17 YEARS OLD, BUT I CANNOT IMAGINE MY FUTURE DOING ANY OTHER JOB. 

To everyone at Scottish Rite Hospital, thank you for everything you’ve done for me. You have completely flipped my fear of hospitals upside-down and I now have the opportunity to live my life pain-free.

Do you have a story? We want to hear it! Share your story with us.