Hemophagocytic syndrome

A classification of rare, non-neoplastic, proliferative disorders of the hematologic system. Primary or familial hemophagocytic lymphohistiocytosis (HLH) is inherited with an autosomal recessive pattern with five known subtypes differentiated by specific genetic mutations. Secondary manifestation of HLH is usually seen in hyperactivated immunologic states such as infection, autoimmune disease or malignancy. Histiocytes in the bone marrow, spleen or lymph nodes become activated to the point that phagocytosis proceeds unchecked. Clinical signs usually present within the first decade and include fever, jaundice, hepatosplenomegaly, lymphadenopathy and skin rash. Prompt initiation of treatment improves survival though prognosis remains poor even with intervention.

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Dhanbad
767 followers

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

User Languages
Speaks Bengali, English, Hindi
359 followers

The Health City Hospital

Intensivist

Maharashtra University of Health Sciences Nashik

bhms

User Languages
Speaks English, Hindi, Marathi
Dhanbad
1572 followers

BCCL Hospital

Ex. Dy.Cmo

PMCH

MBBS

User Languages
Speaks English, Hindi
Atrauli (Aligarh)
317 followers

Parmarth Homeopathic Ausdhalay

M/O Incherge

Homeopathy University Jaipur

DHMS

User Languages
Speaks English, Hindi
Dhanbad
510 followers

Tata Central Hospital, Jamadoba

Consultant Pathologist

SCBMC, Cuttack, Orissa

MD(Pathology)

User Languages
Speaks English, Hindi, Oriya