Hemophagocytic lymphohistiocytosis
A rare but potentially life-threatening disorder characterized by the proliferation of histiocytes and macrophages and phagocytosis of red blood cells, white blood cells, and platelets. It may be inherited or secondary, due to infections, autoimmune disorders, or underlying malignancies. Signs and symptoms include fever, lymphadenopathy, hepatomegaly, splenomegaly, and pancytopenia.
Disease Alternative Name
Ex.central Hospital Dhanbad.1985 ..1993..ex.pathologist .drs Tribedy and Roy Dianostic Lab.kolkata.ex Pathologist.inst of Child Health Kolkata.
Senior Pathologist
School of Tropical Medicine. Kolkata
d c p
20 Years of Teaching To Both UGs & PGs
As Assistant, Associate & Professor
Gandhi Medical College, Dr. NTRUHS
MD Pathology
Dr. Potdar Laboratories
Pathologist
Wanless Hospital
M. D. Pathology
Tata Central Hospital, Jamadoba
Consultant Pathologist
SCBMC, Cuttack, Orissa
MD(Pathology)
Pgimer
M.D (Pediatrics)
Prendas Jalaram and Vallabha Harya and Org Acneilson Marg
Psyhologist
Baroda Medical Collage
Md path
Chalmeda Anand Rao Institute Of Medical Sciences
Associate Professor
Rangaraya Medical College
M.B.B.S., D.C.H
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