21. Answer 1.Alder- reilly anamoly. 2. plasma cells
3. Burkett lymphoma “starlight”
4. Chediak-Steinbrinck –Higashi Anomaly
5. Reed sternberg cells- Hogdkin lymphoma
6. Smudge cells –CLL/SLL
7. ALL
8. AML
9. May-Hegglin Anomaly, associated with giant platelets
10. hairy Cell lymphoma-B cell
11. Sezary- t cell
12. Dsyelomyeloiesis
13. Pelger-Huet Bodies
14. Nuclear extrusion anomaly
15. Dohle bodies
16.Promyelocyte
17. Band
18. Myelocyte
19.metamyelocyte
20. Auer rods

22. Alder-Reilly Anomaly
1.Cytoplasmic inherited abnormalities of neutrophils.
2. Seen in inherited
Hunter’s or Hurler’s syndromes.
3. Heavy granulation.
4. Also seen in mucopolysaccharide storage disease.
5. Caused by an inherited autosomal recessive trait.

23. May-Hegglin Anomaly
Rare, autosomal dominant, qualitative leukocyte abnormality.
Appears as Dohle-like inclusions.
Associated with giant platelets , thrombocytopenia , and slight bleeding tendency.
Cytoplasmic inclusions in May-Hegglin anomaly are PAS negative.
Inclusion found in eosinophils, basophils, monocytes, and neutrophils.
Cytoplasmic inclusions results from structural RNA.

24. Chediak-Steinbrinck –Higashi Anomaly
Rare, autosomal recessive disorder that results in qualitative abnormalities in all types of leucocytes.
Giant , coarse , irregular , peroxidase positive lysosome granules are found in the cytoplasm of granulocytes and monocytes.
Patients demonstrate abnormal pigmentation ,pancytopenia, neuropathies, and recurrent infections.