Welcome to Checking Back with Zac. If you are reading this, chances are you already know a lot about this special little boy. If you don't, I would like to tell you a little about him. Zachary James Moller was born May 1st, 2010 with a condition called Giant Congenital Melanocytic Nevus. This very rare condition affects only 1 in 500,000 so I guess you could say he's one in a half-million.
Zachary James
Monday, December 27, 2010
Starting Out
I am so excited that you decided to learn a little more about my son Zachary's condition. I hope to educate and help people understand this condition as well as the treatments for it with every post. Most people have moles. However, a giant nevus is that on a much bigger scale. Zachary's nevus covers almost his entire back down to the top of his butt. It wraps around the front of his torso. He also has several 'satellites' which are small random nevi in various shapes and sizes all over his little body, a few are pretty big (bigger than a quarter) and a little hairy; most look like he has been splattered with coffee - those nevi are not raised or hairy. He had a few at birth, mostly bigger ones but these little birthmarks just kept multiplying until I couldn't keep count anymore.
A lot of people have wondered why we would bother to have such a large nevus or birthmark removed. I mean, God obviously made this beautiful boy this way...why change a thing. A nevus can be more than just an unattractive, hairy mole. There can be issues with decreased body cooling because the nevus skin has fewer functioning sweat glands and too little fat where the nevus is located (something very scary for the climate we live in). The skin can be extremely delicate and tear easily, requiring restricted activities. People with large nevi have a higher risk of skin cancer.
The second question most people have is how do you remove such a large birthmark. One procedure, the one Zac will be having next week. Is called tissue expansion. The first surgery is done to place an 'expander' under non-nevus skin to expand the skin. The expanders are filled once a week (at home) with a saline for a 12 week period. The bigger the expander, the more good skin you have to replace the nevus skin. When the expander is taken out, the nevus is cut out (several layers) and good skin is pulled over that area. This works better than skin grafting because the expanded skin already has its own blood supply.
The surgeon we have chosen is located in Chicago. Dr. Bauer has been doing nevus removal for over 30 years! So we know Zac will be in good hands. Not to mention, we know that God is looking after Zac and guiding the hands of this most skilled surgeon. These are pictures of the giant nevus on Zac's back. The expander will be placed in his upper left shoulder.
To learn more on this condition, you can visit www.nevusoutreach.org
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What a beautiful little boy, Amy. He is blessed to have wonderful parents like you and Bruce. My thoughts will be with you next week when Zac undergoes surgery.
ReplyDeleteWe just had my ninth child a few days ago and he was born with a giant hairy nevus that covers his entire chest and goes over his right shoulder and onto his back a little. He also has a few satellites that we have found. We know that God will use this for His glory and are waiting to see His plan through this.
ReplyDeleteHe has his first well baby check on Thursday and we will be getting a referral to either UCSF or Stanford.