A 38-year-old male sought my attention this week because of
strange neurological symptoms in the aftermath of a tick bite. He lives in a
small town around Richmond VA. He has
had a lot of tick bites over a period of years, ticks of various sizes. He and
his family love to hike, camp and generally spend a lot of time in wooded area.
In the early Spring of 2015 he found a tick on his calf which he removed.
Within days, he developed a red expanding rash on his upper thigh. The rash encompassed
the entire anterior portion of the upper thigh. He never developed a bull’s eye
rash. The rash was consistently red. The lymph nodes in the groin become
swollen and slightly tender. Within days of the tick bite, he developed an
array of symptoms: fast heartbeat, anxiety, headache, tingling sensations, poor
concentration and others. He went to the ER at the local hospital. He was
diagnosed with panic attack and cellulitis (infection of tissues under the
skin). Lyme disease was dismissed as a possible explanation. Nonetheless, he
was prescribed a week of doxycycline for the cellulitis. He did not improve. He
experienced progressive symptoms: neck pain, back pain, muscle twitches,
strange vibrations, electrical shooting pains, tingling sensations, zapping
sensations. He had a strange feeling of heaviness. He eyes become very
sensitive to light. He developed tinnitus (ringing) in both ears and he became
very sensitive to loud sounds. He noticed poor endurance and fatigue. It became
hard to fall asleep. His cognition felt foggy. Memory was not as good. He had
episodes of spacing out and concentration and focus has been a problem.
He went to his family doctor after a couple of months of
misery. He was quickly evaluated. A few blood tests were done. The patient was
invited back to the doctor’s office after several days and told he had a post-viral
syndrome because EBV (Epstein Barr Virus) titers were high. Lyme
antibodies were negative. The doctor recommended he wait it out. Things would
improve. They didn’t.
In July 2015 he talked his doctor into ordering a whole set
of tickborne disease tests at IgeneX. He was told the results were negative. He
found a local holistic doctor who prescribed a month of 2 antibiotics and
natural therapies. He felt worse. Two doctors now had reviewed the IgeneX
reports and read them as negative.
It is only now that he seeks my help.
At this point the reader might be thinking the Western Blot
results were somehow positive. This would be incorrect. Two doctors had not
looked very carefully at the report. The PCR test for Lyme DNA was positive.
IgeneX notes that the test is not specific for Borrelia burdorferi but may also
pick other forms of Lyme, including B. andersonii, a contender for STARI.
News Flash. As I have been saying, there are other, mostly
unknown species of Lyme. Just this week it was announced: new Lyme organisms
discovered by researchers at the Mayo Clinic, modestly named, B. mayonii.
I believe this patient is infected with a variant Lyme
strain. Therefore, the minimal reactivity on the Western Blot test would be
expected. The positive PCR was a stroke
of luck. Likely vector: lone star tick; likely
pathogen alternative form of borrelia, not B burdorferi.
The diagnosis for this patient could be called Lyme disease.
Borreliosis is a better term as it announces the fact that essentially the same
illness can be caused by other Borrelia species.
By the way: Check out Fitzpatrick’s color atlas of
dermatology. All of the images of EM rash are red patches, just like the
patient had. None are bull’s eye.
5 comments:
What I don't get about Borrelia is the immense variation to antibiotic response.
I don't really know in what world Doxycycline would have zero impact on spirochetes.
The tetracycline class is probably the best broad spectrum antibiotic class of all.
I can agree that doxy might induce blebs, lessen the immune response, kill motile ones and so on.
But no response what so ever?
This antibiotic divergence shows up in lab work too. Zhang claims Tinidazole has little effect in vitro. Sapi and Brorson claim otherwise. How can the results be so different?
I can't take doxy. It causes symtomps to explode. Betalactams work fine however. I had a month of Rocephine, best I ever felt... Some patients are just the opposite.
What treatment are you considering for this patient?
A study some years back done for the now-withdrawn vaccine, with Steere as an author, found that the most common lyme rash was not a bullseye. Somehow that information has never gained any traction. We are still told by the "authorities" that a high percentage of rashes are bullseye, even though the entry to case reporting is a positive two tier test or a bullseye rash. Then a lot of reported cases have bullseye. Gee, if you have to have this to get in the door, obviously the people inside will have it. Once again we ask if this is stupidity or deliberate on the part of the officials.
My rash was small, irregular, red, not expanding. For a long time, I did not associate it with the rest of the symptoms until a doctor showed me an identical rash on his arm where he had removed a tick and then developed lyme symptoms.
Harder to find a rash if you're dark-skinned like myself. or if the bite is on a limb or other area where the shape is not easily discernible.
I've had any number of mysterious small non-bullseye rashes in various places, and at least two such rashes associated with new tick bites and which coincidentally (?)closely preceded the onset of new Sx.
Why did you remove your most recent post dated March 3, 2016, and titled "What the Lyme Western Blot really means, understanding the big picture"? I thought it was very informative and well-written. Now that I no longer have access to it, I wish I had saved it for future reference.
Post a Comment