2002
DOI: 10.1046/j.1365-2141.2002.3317_2.x
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Reversible abnormal chromatin clumping in granulocytes from six transplant patients treated with mycophenolate mofetil: a rare adverse effect mimicking abnormal chromatin clumping syndrome

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Cited by 7 publications
(6 citation statements)
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“…Some less common adverse effects have been reported in children, as follows: an abnormal chromatin clumping syndrome in two children associated with leucocytosis [65]; pseudotumour cerebri syndrome in a 5‐year‐old child taking MMF for autoimmune lymphoproliferative disease [66]; and two cases of children with severe colitis [67]. Perhaps the most significant, albeit rare, adverse effects have been due to respiratory problems, including a single case of reversible chronic mineralizing pulmonary elastosis in a 7‐year‐old boy [68] and several instances of bronchiectasis [69, 70].…”
Section: Unresolved Issues With the Use Of Mmf In Childrenmentioning
confidence: 99%
“…Some less common adverse effects have been reported in children, as follows: an abnormal chromatin clumping syndrome in two children associated with leucocytosis [65]; pseudotumour cerebri syndrome in a 5‐year‐old child taking MMF for autoimmune lymphoproliferative disease [66]; and two cases of children with severe colitis [67]. Perhaps the most significant, albeit rare, adverse effects have been due to respiratory problems, including a single case of reversible chronic mineralizing pulmonary elastosis in a 7‐year‐old boy [68] and several instances of bronchiectasis [69, 70].…”
Section: Unresolved Issues With the Use Of Mmf In Childrenmentioning
confidence: 99%
“…The mechanism of the appearance of ACC is debated although the direct toxic effect of mycophenolate mofetil is one of the hypotheses. In five patients ACC disappeared after tapering or discontinuation of mycophenolate mofetil, confirming that ACC was transient and dose-dependent [ 6 ]. ACC has also been described due to an alteration of the immune status.…”
Section: Discussionmentioning
confidence: 89%
“…Acquired Pelger-Huët anomaly, also known as pseudo–Pelger-Huët anomaly, has morphological features that resemble the congenital anomaly. 15 The acquired anomaly is sporadic, but has been observed in human patients with hematological diseases such as myelodysplastic syndrome, 27,29 and has been associated with the administration of drugs such as sulfisoxazole, 13 sulfadiazine–trimethoprim, 28 valproate, 21 taxoid, 12 immunosuppressive agents, 4,6,9 and ibuprofen. 23 Acquired Pelger-Huët anomaly has also been associated with infections and inflammatory diseases in human beings 5 and animals.…”
mentioning
confidence: 99%