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-   -   Patchy bone marrow cellularity and tongue problems (http://forums.marrowforums.org/showthread.php?t=5117)

jackie8012 Tue Sep 15, 2015 02:09 PM

Patchy bone marrow cellularity and tongue problems
 
Hello my son is 14. He has had sustained bicytopenia affecting his neutrphils and platelets. Plus a white, pitted tongue that had occasional sores on it (since he was five). Because of this he had a bone marrow biopsy. The biopsy showed an unusual picture with reduction in cellularity down to 10% in some areas but normal in others. The aspirate with hypercellular with reduced myeloid and megakeyocytic activity. He has also had a recent ultrasound that showed a 'grainy' liver (he's not overweight) but his bloods have shown that his liver is functioning normally. He also has autism. At present, they do not know what has caused this but have ruled out leukaemia. Any input would be appreciated. thank you

Hopeful Tue Sep 15, 2015 09:47 PM

Hello Jackie8012,

Has your son been tested for dyskeratosis congenita? It is a rare genetic form of bone marrow failure that has many of the symptoms that you have described. Usually there is an abnormality of the nails as well.

It would be important to rule this out before making any treatment decisions. Since it is such a rare disease, it is important to be seen by an expert in bone marrow failure diseases/aplastic anemia. Where are you being seen? I know we have a few UK people here if you need recommendations.

I hope you find some answers.

jackie8012 Wed Sep 16, 2015 05:37 PM

hello, thank you so much for replying to my post. The hospital (in Cambridge, Uk) has just sent a sample off to Oxford in the Uk as apparently they can test for it there. I too have considered dyskeratosis congenita because I looked at thousands of pictures of tongues and the ones that looked most like my son's had that condition. He hasn't however got any problems with his nails. He has another bone marrow biopsy on Monday to see if the cells are improving or getting worse. Will keep you posted. Thanks again for the input - much appreciated.

jackie8012 Wed Apr 26, 2017 09:19 AM

now being tested for dyskeratosis congenita
 
its been a while but my son's bloods are now being sent off to Vancouver to test the telomere length to see if he has dyskeratosis congenita. So worried.

Jacqui Wed May 3, 2017 09:56 AM

Hi Jackie

I have just sent you a private message regarding bloods to Vancouver

Regards
Jacqui


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