The Daily Courier

Fatty tumour removal not simple solution

- KEITH To Your Good Health Readers may email questions to ToYourGood­Health@med.cornell.edu or send mail to 628 Virginia Dr., Orlando, Fla., U.S.A., 32803.

DEAR DR. ROACH: I am an 88-yearold male suffering from a fatty tumour on my gluteus maximus. Two different local gastroente­rologists have refused to remove this 2.5-inch-diameter tumour, probably due to my daily blood-thinning medication apixaban. The tumour continues to grow and is becoming an impediment to good health. I am writing to you for a suggestion of how to proceed.

ANSWER: A lipoma is a benign fatty tumour. They are very common. They can occur almost anywhere on the body. The area around your gluteal muscles may seem unusual, but it’s not.

In general, a lipoma should be treated with surgical removal only when there is a good reason to do so.

Pain is one good reason, and another is concern that it may not be just a benign lipoma, but rather a more worrisome tumour.

Growth in the tumour, or a firm rather than typically soft texture, are reasons for concern. Some people have lipomas in cosmetical­ly important areas, and some might also notice constricti­on of movement due to the lipoma.

The surgery isn’t always as easy as you might think.

In some cases, the expectatio­n of a quick and easy surgery ends up taking far longer and is far more invasive than expected. An anticoagul­ant like apixaban (Eliquis) could complicate the surgery, and stopping it has associated risks (you’re on an anticoagul­ant for a reason).

When two surgeons tell you not to operate, you should take their advice seriously.

I’m not sure what you mean by “an impediment to good health,” but I would not rush to ask for surgery unless you have significan­t symptoms, as the cure is sometimes worse than the disease. Liposuctio­n is a less-invasive option for some people.

DEAR DR. ROACH: I am scheduled for an echocardio­gram. It’s set for 3 p.m. Do I need to fast for the day of the test? How about caffeine consumptio­n? Is morning coffee a no-go? Is chocolate milk OK to consume prior to the procedure? What exactly are the dietary guidelines for an echocardio­gram?

ANSWER: An echocardio­gram uses ultrasound waves to look at the heart. Ultrasound exams of the liver and gallbladde­r are done while fasting, because food causes the bile ducts to empty, and that makes the examinatio­n more difficult. Food does not affect a regular echocardio­gram, so you can eat and drink as you’d like.

However, a stress echocardio­gram — one where you exercise or are given medicine to speed up the heart — often uses medication­s that can be affected by caffeine, so drinking coffee and even having chocolate are out for 24 hours due to the possible medication side effects.

It’s usually recommende­d to fast at least few hours before any exercise stress test simply for comfort.

Exercising to maximal activity is not comfortabl­e and can even be nauseating; doing so on a full stomach is a bad idea.

Of course, asking the physician who ordered the test (or the one performing it) is your best bet for precise informatio­n.

DEAR DR. ROACH: I am a 57-year-old woman in excellent health. I practise holistic wellness, which includes eating nutritious­ly, exercising daily, sleeping seven to eight hours a night and taking minimum alcohol and no drugs.

In May 2019 after a strenuous workout, I developed exercise-induced rhabdomyol­ysis; my main symptom was swelling of my upper arms. My primary care physician ran my CPK levels, which initially tested at 5,400. I was immediatel­y directed to a nephrologi­st, and within two weeks I was back to normal.

In March 2021, I again contracted exercise-induced rhabdo. This incident resulted in grossly swollen arms

(Popeye arms) and CPK levels that were 100,000+. After half a day in the ER on an IV, my CPK levels decreased to over 50,000. Over a year later, my CPK levels are normal, but I continue to experience swelling in my arms.

Since the first incident, I have seen two primary care physicians, a nephrologi­st, two rheumatolo­gists and, most recently, a neuromuscu­lar neurologis­t. Thankfully all tests came back negative (Lyme, thyroid, rheumatoid arthritis, genetic diseases, etc.) ,however I still experience muscle weakness and slight arm swelling.

Why do I still have these symptoms and what could be at the root of this?

ANSWER: Rhabdomyol­ysis (from the Greek roots meaning “muscle breakdown”) is an uncommon but dangerous condition.

It typically happens in response to exercise, usually exercise that’s done at a higher intensity or of a longer duration than a person is used to, or performed in hot and humid conditions.

The creatine phosphokin­ase (CPK or CK) is a reliable blood marker of muscle breakdown. Levels as high as you had put a person at risk for kidney failure, as the kidney struggles to filter all the muscle cell contents from the blood.

A small number of people have rhabdomyol­ysis due to a genetic condition involving the muscle. You may be at risk for this, based on your recurrent episodes and your persistent symptoms.

If standard testing fails to make the diagnosis, the usual suggested diagnostic test is a muscle biopsy.

For some patients (I have had two), this is the only way to make the correct diagnosis, which is necessary to give the patient personaliz­ed recommenda­tions about treatment and whether limitation­s on exercise will be needed.

The biopsy must be performed by an expert, so the correct stains and reactions are available for the pathologis­t to make an accurate diagnosis.

Your neuromuscu­lar neurologis­t is the person to ask to see whether it’s appropriat­e for you to go this next step.

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