This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Chromosomal abnormalities

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Studies reveal a high incidence of non-random chromosomal abnormalities in 70% of cases of ALL and 50% of cases of AML. The genes involved are intimately concerned with the regulation of cell growth.

  • t(9;22), C-ALL; L1 or L2 - more common in adults poor prognosis
  • t(4;11), Null-ALL; L2 - infants; more in girls, high blast count, poor prognosis
  • t(8;14), B-ALL; L3 - hepatosplenomegaly; conventional treatment gives poor prognosis; better with lymphoma type treatment
  • t(8;21), AML-M2 - young; mean age 28 yrs, abnormal eosinophils, solid leukaemic tumours, 75-85% remission when treated
  • t(15;17), AML-M3 - abnormal promyelocytes, 50% develop DIC, durable remissions
  • inv/del/t(16), AML-M4 - 5% of AML abnormal eosinophils 70-90% remission after treatment

Note - t(9;22) is the Philadelphia chromosome.


Create an account to add page annotations

Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.