Showing posts with label medical faq. Show all posts
Showing posts with label medical faq. Show all posts

Tuesday, February 16, 2010

FAQ: Buruli ulcer

Today's Global Health topic: Buruli ulcer. What’s that, you say? Never heard of it before? It’s OK, that’s why it’s one of the World Health Organization’s Neglected Tropical Diseases (more on that below). So consider this a public service announcement of sorts about Buruli ulcers.

Q: What is a Buruli ulcer? (Warning: google image at your own risk)

A: It’s an infection of skin, soft tissue, and bone that is caused by a bacteria called Mycobacterium Ulcerans. Mycobacteria are a unique kind of bacteria, and cause other serious infections (M. tuberculosis causes (surprise!) tuberculosis, and M. leprae causes leprosy). It’s called a Buruli ulcer because of a large study done on it in Buruli, Uganda in the 1960’s.

Q: Can I get it?

A: You can only get infected if you live in tropical wetlands. It’s most commonly found in Africa, but it can be found pretty much everywhere in the world if the climate’s right (It used to be called a Bairnsdale ulcer after Bairnsdale, Australia). No one’s sure how people get infected exactly, but at the moment it’s thought that you have to get bitten by a bug that carries the bacteria in its salivary glands. Yum.

Q: What’s it do to you?

A: The bacteria get into your skin and make toxins that cause cell death (How fun! No other mycobacteria do this). Because the toxins also suppress your immune system, you don’t get any “normal” signs of skin infection, like fever, pain, redness, or swelling, because all these symptoms of infection are actually caused by your body’s normal response to invading bacteria. Because people can have little more than a tiny bump or dark spot on their skin, they ignore it, and the infection is allowed to spread and cause serious problems. Untreated, it can cause severe deformity (again, the google image warning), resulting in permanent disability (the most common site of infection is the legs) and death.

Q: How do you treat it?

A: Antibiotics and surgery. Traditionally, surgery was the definitive treatment (to cut out all the dead tissue), but more recent studies show that if you diagnose the infection and start antibiotics early enough, they can cure nearly 100% of infections, with no need for surgery. But it’s a little tricky to diagnose it at an early stage, because there are no real symptoms that prompt people to seek medical attention, and there’s really no good diagnostic test for it, especially one that could practically be used in the rural, resource-poor areas where this infection is endemic.

Q: What’s a Neglected Tropical Disease (NTD)?

A: The World Health Organization has made a list of diseases that affect a large number of people worldwide, with high morbidity and mortality, yet receive relatively little funding and attention. The NTD’s affect one billion people, and together cause 534,000 deaths per year. From the WHO’s website: “Those most affected are the poorest populations often living in remote, rural areas, urban slums or in conflict zones. With little political voice, neglected tropical diseases have a low profile and status in public health priorities.” NTD’s affect 1 in 6 people worldwide. To compare that number to a disease that gets more press time, 1 person in 1,762 has Mutiple Sclerosis. (Ever heard of trachoma? Eight million people are blind because of it. Filariasis? Chagas' disease?) See their website for more info.


Such a pretty lake, but potentially so deadly: Lac Zilé, near Lambaréné, Gabon.



The story of Buruli ulcers in Lambaréné

Although I was doing adult medicine (and BU mainly affects children), I became interested in BU because of the several children who literally lived in the surgery ward, where they were under long-term treatment for the ulcers. All patients at the hospital were cared for by a family member, who was responsible for cleaning, buying and cooking food, giving medications, and many of the jobs that nurses in the US do for patients (even including taking and charting temperatures). Because these kids were there so long-term, they could not have a family member stay with them, so they were essentially on their own. We befriended three of the girls in particular (their picture is in another post), whom I would sometimes sneak away after rounds to visit, or would come over to our house on the weekends.

In the morning, one or two of the girls could be found sweeping the small stoop outside their rooms (all of the rooms opened into a main hallway inside, and had a door to the outside), or washing their sheets and spreading them out on the lawn to dry. I had difficulty picturing American tweens fending for themselves, cleaning their own hospital rooms, entertaining themselves, and finding their own food (even without one arm completely bandaged up). One evening after afternoon rounds, my attending and I passed the entire group of children, most of whom had Buruli ulcers, playing soccer on the large lawn between the surgery and ob/gyn wards. Most were running around, screeching and laughing and playing, enjoying the setting sun with their friends; only two boys sat watching from their wheelchairs, as neither had walked in several months due to surgical debridement for BU that spanned their legs from their hips to their toes. I was truly touched during the three months we knew the girls at how they created a normal childhood for themselves despite their disabling disease: constantly spending time together, choreographing dances to their favorite pop songs, and throwing birthday parties for their friends on the lawn outside the surgery ward.

One afternoon I left the three girls on our porch, and came home to find my camera filled with literally hundreds of pictures they had taken of each other, capturing their adolescence in a way no photographer never could. Looking at these pictures now (I couldn’t bring myself to delete even one) makes my heart break. They are only a few years younger than, but a lifetime removed from, the many young women that would come into clinic with the outlines of their skeletons visible and CD4 counts in the single digits, who would die overnight or the next day from AIDS. So what’s happened to these three girls? They were all discharged within one week of each other in late July, and I only hope they have stayed healthy since then.


Wednesday, May 21, 2008

FAQ: glioma vs glioblastoma

Been getting a couple questions about brain tumors lately. Obviously because of Ted Kennedy (so sad) but also because of a family member recently diagnosed with glioblastoma (also very sad). Here goes:
A glioma is a tumor that arises from cells in the brain called glial cells. Basically these are all the cells in the brain that aren't neurons; they are the "glue" that holds the neurons together. Any tumor that comes from glial cells is called a glioma. But each kind of glial cell (for example astrocytes or oligodendrocytes) can have its own tumor arise from it, and each tumor has its own name. A tumor arising from astrocytes is called an astrocytoma. A tumor arising from oligodendrocytes is called an oligodendroglioma. These are types of gliomas.
Astrocytomas comprise 80% of primary brain tumors in adults. (Primary simply means that the tumor doesn't originate as cancer somewhere else in the body and metastasize to the brain.) There is a spectrum of badness for astrocytomas. Grade IV astrocytomas are the most aggressive and have a special name: glioblastoma. (I didn't come up with this naming system, people.)
Contrary to popular belief (or my interpretation of popular belief, I guess), brain tumors rarely present with headaches. This is because there are NO nerve endings in the brain, so tumors don't cause pain. Crazy, right??? (If there was some way to get inside your skull pain-free, you could undergo brain surgery without anesthesia.) They usually present in one of two ways: with seizures (a la Ted Kennedy), or with something called mass effect. Mass effect means the signs and symptoms that arise from having a mass in the brain, since the brain really doesn't like to be pushed around inside the skull. Symptoms include mostly nausea and vomiting, though a classic sign is vomiting without nausea. One more time: headaches rarely mean brain tumor.
Hmmmm....any other burning questions about brain tumors?....

Thursday, February 28, 2008

Nec fasc./Flesh-eating bacteria/Chompers

"Necrotizing fasciitis. Explain...with pictures please."
Many names for one nasty disease. Necrotizing fasciitis is a type of deep tissue infection. (Fascia is the stuff between and around all your organs and muscles and blood vessels. Fasciitis is an inflammation of the fascia. Necrotizing means it kills cells and tissues.) It's caused by toxins that are produced by certain strains of bacteria, the most common of which is Group A Streptococcus (Group A strep is also known as Strep pyogenes and as GAS). There is no one type of bacteria that causes nec fasc. The bacteria destroy the deep tissue of the body, and it's fatal if not treated quickly and effectively.
Keep this bacteria away from me, please.
You might have toxin-producing GAS all over your skin right now, for all you know. (sleep tight!) But people who carry bacteria on or in them don't necessarily develop infections. Certain people can develop infections after surgery, or because they have breaks in the skin (like with eczema), or because they have a weakened immune system. Only very rarely do people actually develop necrotizing fasciitis.
So how do I know if I have it??
There are no specific symptoms, which makes it a bugger to pick up. And it progresses rapidly and is fatal if not treated quickly enough. Initial symptoms are similar to those of a soft-tissue infection, such as pain, swelling, or redness. But the infection doesn't always occur where the bacteria get in (like an open cut on your hand). They can travel around your bloodstream and set up shop anywhere they'd like.
A rapidly fatal disease with nebulous symptoms sounds like a nightmare to diagnose.
But that's what makes medicine fun! Sometimes you can put on your monacle and play Sherlock.
This sounds familiar...where have I heard of nec fasc before?
It's in a 'Scrubs' episode, where JD correctly diagnoses his patient with it (which he calls "Chompers") after watching a Friday night TV special on it. There was a recent article in The Boston Globe Magazine about a woman from central MA who developed this infection after having a C-section, and is now a quadruple-amputee (yes, you read that right). You can read about her amazing story here.
What about those pictures?
No way am I posting pics here. Google image "necrotizing fasciitis" at your own risk.
So how do you treat it?
Surgery! All of the dead and infected tissue has to be cut out, along with a margin of healthy tissue. Plus some potent antibiotics. Still, the mortality rate is 30%.
That's gross.
Yes. It is.

Wednesday, February 27, 2008

Medical FAQ

So what does ringworm look like?
It looks like a reddish ring on the skin. Like this or this. It can also be lighter than the skin color. The border is usually slightly raised and red, and the center is flat and lighter (so if you run your finger over it, you can only feel the edges). It can be found in areas of lighter hair growth, or, alternately, it may be in an area with some hair (like the forearm) but have no hair growing within the ring.
So it's a worm infection?
Nope, it's a fungal infection. Unclear etiology of the name ringworm, however, except that it's in the shape of a ring.
How do you get it?
Any type of contact with kids'll do it.
Ew, get it off me!
You can use any topical (meaning you put it on your skin) over-the-counter antifungal, like Monistat.