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Welcome to another Inside Lyme Podcast. I am your host Dr. Daniel Cameron. In this episode, I will be discussing a question I’m asked frequently: What does a Lyme disease rash look like? As a new study has found, the erythma migrans rash can appear differently based on several factors.
The study by Rebman and colleagues, entitled “The presenting characteristics of erythema migrans vary by age, sex, duration, and body location,” was published in Infection in March 2021.¹ It addressed a frequently asked question: What does a Lyme disease rash look like?
The erythema migrans (EM) rash (or Bull’s-eye rash), considered a definitive sign of Lyme disease, is often mistakenly thought to appear similar in all individuals – a circular red lesion which expands to at least 2 inches.
But as Rebman and colleagues report, a Lyme disease rash can look different based on several factors and does not always appear as the familiar Bull’s-eye rash. In fact, the authors suggest that relying solely on a Bull’s-eye appearance, when evaluating a rash for possible Lyme disease can lead to delays in diagnosis and treatment.
Diverse characteristics of Lyme disease rash
The authors examined 271 Lyme disease patients who had an erythema migrans rash to determine what does a Lyme disease rash look like? ¹
“We studied associations between these presenting characteristics [of EM rashes], as well as whether they were associated with age, sex, EM duration, body location, and initiation of antibiotics,” the authors write.
The patients were part of a longitudinal cohort study from 3 sites in Maryland and southeastern Pennsylvania. They were not enrolled if their rash was under 5 cm in diameter (2 inches) or their acute illness was longer than 3 months.
The study found that:
- EM size increased over time with the EM duration peaking at 14 days.
- Males had larger rashes than females (an average of 2.8 cm larger).
- Males were more likely to have a blue/red rash. In fact, the odds of a red rash in males was 65% lower than in females.
- Age was a significant predictor of central clearing. For every 10-year increase in age, the odds of central clearing decreased 25%. As age increased, there was a greater likelihood of a solid rash.
- EM rashes were more likely to occur in harder to see body locations (i.e., behind the thigh and behind the knees). The authors assumed that ticks had an opportunity to attach longer in these areas before being discovered.
- Nearly 1 in 3 patients had multiple rashes on examination.
- Approximately 1 in 3 patients reported pain at the site of the rash.
- Just over 50% of the EM rashes were itchy.
- Rash shapes were varied ─ 50.9% were round; 39.1% were oval. The remaining rashes were irregular.
- Rash colors were varied ─ about 3 out of 4 were red. The remaining rashes were blue/red.
- Rash patterns were varied ─ only 28% appeared as a Bull’s-eye rash (a ring within the rash). Central lightness (17.3%), central darkness (28.8%) and uniform rashes (25.8%) were also described.
- Over 90% of the rashes were homogeneous. The remaining rashes were uneven.
- Nearly 9% presented with vesicles.
Concerns with limiting size of Lyme disease rash
The authors raised concerns with following a 5 cm (or less than 2 inches) cutoff for EM rashes in determining the presence of a Lyme disease infection.
“Applying a 5 cm size cutoff in research or surveillance settings may thus exclude a higher proportion of females with otherwise suggestive clinical histories and epidemiological risk,” the authors write.
They also raised concerns about recognizing an EM rash in darker skinned patients. “95.9% of our final sample self-identified as non-Hispanic white.”
The authors suggest that the variation in EM rash presentations in males vs. females and among various ages may be related to an immune response to the Borrelia infection.
Authors’ Conclusion
“Given that EM remains a clinical diagnosis, it is essential that both physicians and the general public are aware of its varied manifestations.”
Editor’s note
Unfortunately, fewer than half of Lyme disease patients present with an erythema migrans rash. This case series merely reflects the diversity of rashes in Lyme disease patients fortunate enough to present with a rash.
The following questions are addressed in this episode:
- What is an erythema migrans rash?
- How often do Lyme disease patients have an erythema migrans rash?
- Can you culture Lyme disease from a rash?
- How long do erythema migrans rashes last?
- What other rashes resemble an erythema migrans rash?
- What color rashes have you seen?
- Where are rashes located?
- What is the significance of multiple rashes on examination?
- Have you seen itchy erythema migrans rashes?
- Can you discuss diversity of erythema migrans rashes that were described?
- Could a rash less than 2 inches in diameter be important?
- What do we know about the appearance of rashes in people of color?
- What is the importance of a smaller rash in women?
- Thanks for listening to another Inside Lyme Podcast. You can read more about these cases in my show notes and on my website @DanielCameronMD.com. As always, it is your likes, comments, reviews, and shares that help spread the word about Lyme disease. Until next time on Inside Lyme.
Please remember that the advice given is general and not intended as specific advice to any particular patient. If you require specific advice, then please seek that advice from an experienced professional.
Inside Lyme Podcast Series
This Inside Lyme case series will be discussed on my Facebook page and made available on podcast and YouTube. As always, it is your likes, comments, and shares that help spread the word about this series and our work. If you can, please leave a review on iTunes or wherever else you get your podcasts.
References:
- Rebman AW, Yang T, Mihm EA, et al. The presenting characteristics of erythema migrans vary by age, sex, duration, and body location. Infection. Mar 7 2021; doi:10.1007/s15010-021-01590-0
I live in Canada and was infected in France while I was visiting my daughter who lives there. The rash was an expanding oval rash. Didn’t look like a bullseye so I thought I was OK. When I saw a Lyme Doctor in the USA (Canada has none) she said any rash of any kind after a tick bite is a sign of trouble. I say that needs to be made public knowledge. I would have gone to a doctor in France or at least as soon as I came home if I had known.
For sure, I got bit in Traverse City MI on a family trip 4 yrs ago, in live in AZ and lyme does not exist here and was treated by doctors that said I had cellulitis and/or shingles, rash did not go away and went to thr ER and a bullseye was spotted at the ER and Dermatologist Office, I begged them and they finally put me on doxycycline for two months, it made the rash finally disappear but 3 years later I still get swelling in my one leg and ankle and pain and brain fog. I hope you were able to at least get on some sort of medication. My brother got bit by a tick in Michigan, he did not get lyme but another tick issue and after several doctors, he got one to put him on minocycline for two years. sorry about spelling. I wish you luck and that you are ok.
I have what looks like Erthema Migrans Rash. They keep telling me I test negative for Lyme. My speech is now effected and I was diagnosed last Sept with a tick borne illness that made me very sick. soon after that I developed red spots on both wrist with hard centers. Soon after that this happened on my left breast, left side of my belly and all around my groin. I am at wits end to figure out if this is due to Lyme, most doctors I’ve been to dismiss it when I bring it up. I live in Vt. and would like to see a Lyme specialist but insurance won’t cover it unless diagnosed. Anyone know the next step. They want to send me to a dermatologist and sleep study. I already have seen a neurologist and did not have stroke. I’m 61 and feeling crappy all the time. No energy ,wake up feeling tired. I seem to loose balance and sometimes trip easily. Hot Flashes, slurred speech and my brain does not work well in the afternoon.
You also need to write about the different rash you get in Europe (expanding oval rash from Borrelia garinii).
There are Canadians who have family in the UK, France and Germany and visit them once a year for a month.