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Diagnostic value of bone marrow cell morphology in visceral leishmaniasis-associated hemophagocytic syndrome: Two case reports. | LitMetric

AI Article Synopsis

  • Visceral leishmaniasis-related hemophagocytic lymphohistiocytosis (VL-HLH) is a rare and severe infection that can lead to high mortality rates, especially in nonendemic regions, where timely diagnosis is crucial for effective treatment.
  • A case study involving two young girls with repeated fevers and severe symptoms revealed that despite initial treatments for suspected malignancies, they were ultimately diagnosed with VL-HLH through bone marrow examinations that identified specific pathogens.
  • The study emphasizes the importance of bone marrow morphology in diagnosing VL-HLH and recommends that such examinations be conducted early and repeatedly in young patients to avoid misdiagnosis and improve treatment outcomes.

Article Abstract

Background: Visceral leishmaniasis related-hemophagocytic lymphohistiocytosis (VL-HLH) is a hemophagocytic syndrome caused by infection. VL-HLH is rare, especially in nonendemic areas where the disease is severe, and mortality rates are high. The key to diagnosing VL-HLH is to find the pathogen; therefore, the must be accurately identified for timely clinical treatment.

Case Summary: We retrospectively analyzed the clinical data, laboratory examination results, and bone marrow cell morphology of two children with VL-HLH diagnosed bone marrow cell morphology at Kunming Children's Hospital of Yunnan, China. Both cases suspected of having malignant tumors at other hospitals and who were unresponsive to treatment were transferred to Kunming Children's Hospital. They are Han Chinese girls, one was 2 years old and the other one is 9 mo old. They had repeated fevers, pancytopenia, hepatosplenomegaly, hypertriglyceridemia, and hypofibrinogenemia over a long period and met the HLH-2004 criteria. Their HLH genetic test results were negative. Both children underwent chemotherapy as per the HLH-2004 chemotherapy regimen, but it was ineffective and accompanied by serious infections. We found amastigotes in their bone marrow morphological examination of their bone marrow cells, which showed hemophagocytic cells; thus, the children were diagnosed with VL-HLH. After being transferred to a specialty hospital for treatment, the condition was well-controlled.

Conclusion: Morphological examination of bone marrow cells plays an important role in diagnosing VL-HLH. When clinically diagnosing secondary HLH, VL-HLH should be considered in addition to common pathogens, especially in patients for whom HLH-2004 chemotherapy regimens are ineffective. For infants and young children, bone marrow cytology examinations should be performed several times and as early as possible to find the pathogens to reduce potential misdiagnoses.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210904PMC
http://dx.doi.org/10.12998/wjcc.v10.i16.5463DOI Listing

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