1Assistant Professor, M.N.J Institute of Oncology & Regional Cancer Centre, Osmania Medical College and General Hospital, Hyderabad, Telangana, India
2Professor, M.N.J Institute of Oncology & Regional Cancer Centre, Osmania Medical College and General Hospital, Hyderabad, Telangana, India
3Senior Lecturer, Department of General pathology, M.N.J Institute of Oncology & Regional Cancer Centre, Osmania Medical College and General Hospital, Hyderabad, Telangana, India
*Corresponding author email id: aparna.akella@yahoo.com
Online published on 12 August, 2019.
To study the co existence of Hodgkins lymphoma in sickle cell disease in a 10-year-old boy who is also a known case of sickle cell anaemia presented to out centre with symptoms of fever, weight loss. History of previous blood transfusions was given. On clinical examination, he was found to have pallor, generalised lymphadenopathy, splenomegaly. Complete blood picture revealed haemoglobin of 9 g/dl, white blood cell count of 12,000/cu mm, platelet count of 2 lakhs. Biopsy from the cervical lymph node revealed effacement of lymph nodal architecture with replacement by scattered atypical mononuclear and binucleate Reed–Sternberg cells with moderate cytoplasm, large vesicular nucleus and prominent eosinophilic nucleoli against a background of, mixed population of small lymphocytes, plasma cells and few eosinophils. Immuno histochemistry revealed positive expression of CD15, CD30, Pax-5 in the atypical cells and thus proved to be Hodgkins lymphoma.
Sickle cell disease, Hodgkins lymphoma, Hodgkins lymphoma in sickle cell disease, Nodular sclerosis, Epstein–Barr virus, Reed–Sternberg (HRS) cells
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