Volume 43, Issue 6 pp. 1443-1450
ORIGINAL ARTICLE

A hungry Histiocyte, altered immunity and myriad of problems: Diagnostic challenges for Pediatric HLH

Akriti Gera

Akriti Gera

Department of Pediatrics, VMMC and Safdarjung Hospital, New Delhi, India

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Aroonima Misra

Aroonima Misra

Indian Council of Medical Research, National Institute of Pathology, New Delhi, India

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Aditi Tiwari

Aditi Tiwari

Department of Pediatrics, VMMC and Safdarjung Hospital, New Delhi, India

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Amitabh Singh

Corresponding Author

Amitabh Singh

Division of Pediatric Hematology/Oncology, Department of Pediatrics, VMMC and Safdarjung Hospital, New Delhi, India

Correspondence

Amitabh Singh, Division of Pediatric Hematology/Oncology, Department of Pediatrics, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi 110029, India.

Email: [email protected]

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Sumit Mehndiratta

Sumit Mehndiratta

Division of Pediatric Hematology/Oncology, Department of Pediatrics, VMMC and Safdarjung Hospital, New Delhi, India

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First published: 12 June 2021
Citations: 1

Gera and Misra are Joint first authors and both contributed equally.

Abstract

Introduction

Hemophagocytic lymphohistiocytosis (HLH) is an immune deregulation disorder with varied clinical presentation which clinically overlaps with widespread tropical infections.

Methods

We conducted a retrospective chart review of children diagnosed with HLH at our center from February-2017 to October-2020.

Results

Out of the nine diagnosed patients, genetic predisposition was present in three children; two had identified infectious triggers. The mean age of presentation was 30 months with male predominance. The most common clinical findings were fever, organomegaly, and pancytopenia. The median value of fibrinogen was-156 mg/dL, ferritin-12 957 ng/mL and for triglycerides-349 mg/dL, respectively. In children with identified genetic predisposition, serum ferritin levels were usually more than 10 000 ng/mL. The majority of our patients had evidence of hemophagocytosis on bone marrow examination. In our experience, although nonspecific, very high ferritin and serum triglycerides with low fibrinogen in a patient with bi-cytopenia, pancytopenia was the most suggestive evidence of HLH. Genetic evaluation in our series identified three children, one with primary HLH genetic mutation and two with underlying immune deficiency syndrome. The presence of HLH in the accelerated phase of Chediak-Higashi and AD Hyper IgE syndrome with HLH is extremely rare. Leishmaniasis (in nonendemic area) and Ebstein-Barr virus (EBV) was identified as an infectious trigger in two cases. Most of our cases received treatment as per HLH 2004 protocol. Three children died during the initial diagnosis and treatment. HLH with subcutaneous panniculitis-like T-cell lymphoma recovered well.

Conclusion

HLH remains a life-threatening disorder associated with a variety of underlying illnesses as highlighted by our case series.

CONFLICT OF INTEREST

All authors wish to declare no conflict of interest.

DATA AVAILABILITY STATEMENT

Data sharing not applicable – no new data generated.

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