Morton’s Neuroma Revisited
Thank you all so much for your comments and support. I have received a lot of feedback and fantastic questions about Morton’s neuromas (MN) and your problems with diagnosis and treatment of such. This area of the foot can indeed be terrifically confusing and difficult to diagnose. I want to help you all as much as I can with this conundrum, and I would love to answer each and every one of you individually, but I just can’t and shouldn’t in this setting.
If you have been labeled with the diagnosis of a Morton’s neuroma and various treatments are not working so well, maybe you don’t have a Morton’s neuroma.
The MN diagnosis is made way too often. Why? Here are some misconceptions that surround the dreaded Morton’s neuroma that can lead us astray:
MN’s are really common. Actually they are not common, especially a 2nd web space MN (15%, I think almost ZERO percent). Even 3rd web space MN are not common. If your doc is indicating a 2nd web space MN, question it and consider the much more common 2nd MTP synovitis (inflammation of the central ball joint). If they are thinking 1st or 4th web space, RUN.
MN diagnosis is SEXY. We docs just got to make that diagnosis. “You have a Morton’s neuroma”. It has teeth. It sounds so definitive and sure. It is like a golf ball set up on a tee just waiting to be shanked.
MN’s are easy to diagnose. Actually, they are not easy to diagnose. I have done this for 27 years and now more than ever, I am now even more cautious and I respect making this diagnosis more than ever. It is actually a diagnosis of exclusion. This means that I rule out the other possibilities to the best of my ability before making the call of a MN. Too many good docs jump right to this diagnosis. It has to be the last diagnosis, and even then I am often not as sure as I would like to be normally.
“You have a Mulder’s click”. This is a physical finding that is rarely helpful, but boy, do love it.
The MRI and more recently, ultrasound have not helped matters either. In fact, those who rely on these tests are trying to increasingly make a claim regarding their diagnostic prowess, which is not true. Stick to old fashion history and exam.
MN may be all your doctor knows.
Basically, central forefoot (2nd, 3rd, 4th metatarsal head region, not 1st or 5th) pain that starts in an otherwise normal foot can be divvied up into four basic diagnoses the great majority of the time. There are several more diagnoses that are uncommon and frankly, outliers that are not discussed here such as Freiberg’s infraction, inflammatory arthritis (rheumatoid), etc. Here are the names and the diagnostic criteria, according to the AO. Keep in mind that the majority of these can be diagnosed by history alone and an MRI or an ultra sound is generally not needed in any of these. In fact, they are a waste of time and money. If your doc is quick to say they need an MRI to make the diagnosis consider another route. I’m not sayin’, I’m just sayin’. Exam is important, but only to support and confirm the history. By the way, no matter what you think or hear, none of these ever have a history of actual causative acute trauma. If you have a history of trauma and you have one of these I would say True-True-Unrelated. Finally I am not discussing treatment. The treatment of each of these is clearcut as long as one is confident in the diagnosis, which what this is about. Intractable plantar keratosis (IPK) or plantar corn or callus
Generally older, 50 yo plus, but can be any adult
Pain is on the bottom
Insidious slow onset, present for some time
Visible seed, small tight callus that is exquisitely tender to touch.
No swelling
You would have to be brain dead to miss this one.
Pain only with weight bearing
Worse on barefoot, better in shoes
When it comes to trauma, this one could be the exception. If there is bonafide past or remote trauma to your foot/metatarsal or previous surgery that leads you to have a residual unevenness to the weight bearing surface of your metatarsals, then you could develop an IPK form that.
X-rays negative
Can be confused with a plantar wart.
Metatarsal neck stress fracture
Ages
Military recruits, boot camp, “march fracture”
Distance runners, any age, training error
50+ female>>male
Recent rapid onset
Recent rise in activity level, especially number of steps! Normal activity to many more steps per day, vacation, new exercise program, etc. Or lower activity as in being down from prolonged inactivity, i.e.illness, heading back to your normal activity level. Jumping out of the back of a pick up truck and breaking your metatarsal is an acute fracture, not a stress fracture, and is different.
Pain on top of foot
Swelling top of foot
Usually 2nd metatarsal, next to big toe metatarsal
Pain with weight bearing, with or with out shoes
X-rays negative in first 21 days, then new reparative bone formation is seen and sometimes the fracture is seen.
Morton’s neuroma
Adults, peak age 40’s thru 50’s.
Insidious onset, often years.
Unlike all the others, at first and often even later, the location of the pain can be vague; can’t pinpoint. Can be frustrating for patient and doctor alike. However, knowing this can ultimately be helpful if used correctly.
Pain mostly on bottom.
Can take a while to get started with standing/walking.
Worse in confining shoes, better in sandals or barefoot.
NO SWELLING..............EVER. Whoops, caps lock on again.
Can feel swollen however. Numbness can feel like swelling. Remember the last time you got home from the dentist and you looked in the mirror because you were sure that your tongue was hanging out of your mouth only to find out all was well. I rest my case.
There can be a sensation of actual, perceptible numbness between the two affected toe which border the neuroma. This sensation or finding by your doc is extremely variable and unreliable. It’s presence or absence really means nothing. I ignore it basically except to support my other findings.
Mulder’s click is a useless finding. It’s absence means nothing. While I do dismiss it, a Mulder’s click may be supportive if when performed it exactly recreates your pain.
3rd web...85-90%, 2nd web 10-15%, 1st or 4th web.......not.
These are two things that get my attention and often have meaning, but only supportive with other findings and history:
feeling of folded sock bottom of foot
urge to take off shoes and rub foot. Does not matter whether you actually ever do it, it is just the urge part.
Second MTP synovitis (AKA, capsulitis, pre-dislocation syndrome)
Majority in specific demographic, 55 +/- yo female
Not mentioned as differential diagnosis on Mayo or WebMD sites, but capsulitis is right there on Wikipedia.
By and far the most common of these four diagnoses
Primarily 2nd metatarsal. Infrequently the 3rd.
Insidious onset, few days to weeks.
Swelling top and bottom often, but not always.
Painful “lump” or “rock” under ball of foot. Pain on bottom.
Worse on hard floor barefoot, better on carpet or cushioned shoes.
Sometimes there is the perception of some form of trauma, but any trauma is just the “straw that broke the camels back” phenomenon. For instance dancing at a wedding in heels to get it started. But here is something you MUST know; it was going to start eventually anyway because it is a result of:
mostly these occur as a result of calves that are too tight which places more pressure on the forefoot/metatarsal heads. This represents a more recent change and why this is happening now and not before.
In a very small part due to the anatomy because the 2nd metatarsal is the most prominent in almost all of us. This has been your anatomy forever and has not changed. Your doctor might refer to your 2nd metatarsal that is “too long”, but it has been that length all your life. Seriously, it isn’t as if your metatarsal magically grew longer recently. Now, refer back to calves.
Transfer metatarsalgia secondary to a bunion. Often blamed, but the calves that are too tight are the larger reason this is going on at this point in your life.
When this problem is left untreated, eventually a hammertoe will develop if the swelling is allowed to persist. Hey, here is a novel idea. The great majority of isolated 2nd and/or 3rd hammertoes result from MTP synovitis which comes from calves that are too tight, which is almost completely preventable as long as you stretch your calves.
Often the inflammation from the 2nd MTP synovitis can irritate the adjacent 2nd web space nerve causing neuritis, which is a secondary thing and not a Morton’s neuroma. If you are reading this, chances are you fit in one of these four groups. Certainly you’ve gotten loads of information from the stranger on the bus next to you, or your nosey neighbor (everybody is an expert), or from the internet, or even your doctor. Again, the mere fact that you are reading this means things probably aren’t going so well. No matter what you have heard from these random sources statistically your problem is second MTP synovitis, and not a Morton’s neuroma.
MyRightFoot on January 5, 2013 at 8:05 pm
I was diagnosed w/ Mortons Neoroma 8-9 yrs ago. Dr. wanted to perform surgery that sounded extreme. No Way! Tried custom orthotics – worthless; pads on ball of foot provided relief along w/ more comfortable footwear, but problem still there and seriously affecting my comfort when walking. Different foot doctor diagnosed MN again (between toes 2 & 3, right foot) and he discouraged surgery. He performed cortisone / alcohol injections 4 times over a period of 2-3 months. To this day, I’m happy to say that it is 98% “cured”. Only very occasional discomfort with certain types of shoes and when barefoot on hard surfaces. Glad I didn’t go for surgery. Moral: get…
Kirt on January 9, 2013 at 12:08 am
Left foot pain between 2nd and 3rd metetarsal x 2 years. MN removed in 2012. Still having foot pain. Expensive orthodics, steroid injections and PT and nothing has made it better. My work requires me to stand at an exam table up to 4-6 hours at a time without sitting. Pain is terrible. I am wearing the widest shoe possible with no relief. Only relief is when I have no shoe on. Physician who did my surgery says ” I have to live with it and there is nothing more that can be done”. Looking for answers. saw that some Physician is doing nerve removal and re-transplant. Any suggestions? Also what is the…
Russell Rottino on August 16, 2012 at 7:39 pm
I have PF in both feet. I have done everything possible you can do for PF. That is, stretching, cortisone shots, epidurals, boots, every kind of orthontics ever made, and finally surgery on the left foot. Nothing! Still live with the pain. Now I have MN between 2 and 3 on the right foot. Sucks to be me. I found another podiatrists recently and he tells me he can fix the PF once and for all. He cuts the faciia all the way across. Completely severes it. Most sergeons will only cut 1/3. I have never heard of this before. By the way. If you do have Plantar Faciitas, the best shoes…
Shelley on July 17, 2012 at 6:49 pm
Thank you for such great info. I had surgery for MN over 3 years ago and my foot hurts just as bad as well as my entire right leg from walking differently I guess. I have pain everyday…all day and even during the night. My Dr said I may need the second surgery which is done from the bottom of my foot and has a longer recovery time. As it was my first surgery took 3+ months of recovery. My initial instinct with regards to my Dr should have made me look for someone else to do the surgery. At one point he was giving me a cortisone shot in my foot from…
Hanie Hartman on May 15, 2012 at 8:33 am
Hello,I have had pain between toes three and four that was diagnosed as a morton’s neuroma last summer. Since I have also had bunions for MANY years, I had surgery to fix the bunion and remove the morton’s neuroma in August of 2011.I still have pain in the front of my foot whenever I walk/run. It is mostly between toes two and three. The key word here is ‘mostly’. I also occasionally have pain/burning between one and two. I also occasionally have pain across the back part of almost the entire ball of my foot. In February of 2012, I had surgery to remove the pin for the bunion surgery. Then I…