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
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Top doctors who continously share their opinions on Hemophagocytic lymphohistiocytosisEx.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)
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Please share your overall clinical experience with the Ibuprofen + Paracetamol combination in treating Paediatric Fever and pain?
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Penile fracture or rupture is a rare event but requires urgent diagnosis and intervention. It is a rupture of the penile albuginea of the corpora cavernosa or corpus spongiosum due to trauma to the erect penis, most commonly during sexual intercourse. Dr. Vivek Jha is sharing a clinical case of “Penile Fracture” managed with surgical expertise by him. Share your views on the case & learn new things.
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M.22yrs. Findings and Diagnosis please.
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F.52yrs. Haemoptysis,cough Chest pain 1month.
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M.16yrs. Pain both feet 8 days.
Dr. Syam Sundar Patro1 Like4 Answers
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