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#1
Tue Sep 15, 2015, 03:09 PM
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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
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#2
Tue Sep 15, 2015, 10:47 PM
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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.
__________________
58 yo female, dx 9/08, AA/hypo-MDS, subclinical PNH, ATG/CsA 12/08, partial response. small trisomy 6 clone, low-dose cyclosporine dependent
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#3
Wed Sep 16, 2015, 06:37 PM
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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.
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#4
Wed Apr 26, 2017, 10:19 AM
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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.
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| Thread | Thread Starter | Forum | Replies | Last Post |
| bone marrow reduction in cellularity and patchy, problems with tongue | jackie8012 | Pediatrics | 0 | Tue Sep 15, 2015 09:38 AM |
