Hypoplastic Bone Marrow Failure in a Patient with Hereditary Persistence of Foetal Haemoglobin (HPFH) Trait
Hereditary Persistence of Foetal Haemoglobin (HPFH) trait is a rare genetic disorder and is caused by a large deletion involving δ and β globin genes. It is characterised by persistence of Foetal Haemoglobin (HbF) even in an adult. HbF level may vary from 2 to 30% in carriers of HPFH. Clinically, HP...
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doaj-7d4c43e9d4314a37b7ee87352b308f3c2020-11-25T02:30:47ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2020-03-01143ED01ED0210.7860/JCDR/2020/43368.13546Hypoplastic Bone Marrow Failure in a Patient with Hereditary Persistence of Foetal Haemoglobin (HPFH) TraitAK Kapoor0S Maurya1Geeta2Pathologist, Department of Pathology, Vivekananda Polyclinic and Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.Director and Head, Department of Pathology, Vivekananda Polyclinic and Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.Technologist, Department of Pathology, Vivekananda Polyclinic and Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.Hereditary Persistence of Foetal Haemoglobin (HPFH) trait is a rare genetic disorder and is caused by a large deletion involving δ and β globin genes. It is characterised by persistence of Foetal Haemoglobin (HbF) even in an adult. HbF level may vary from 2 to 30% in carriers of HPFH. Clinically, HPFH trait is asymptomatic without relevant haematological alterations. Mostly, HPFH trait is detected incidently while screening for other haemoglobinopathies. Herewith, we report a case of HPFH trait in our population. A 10-year-old boy born of non-consanguineous marriage complained of dyspnoea on exertion and dizziness. On examination he had generalised pallor. Earlier, he gave history of exposure to pesticides while spraying on crops. Later, he developed neutropenia (neutrophils 2000/mm3). He was immediately treated with piperacillin and gentamicin. Later, he was found to be severely anaemic (haemoglobin 3.0 gm/dL). His serum ferritin was within normal range. He also had severe thrombocytopenia (Platelets 10×109/L). Subsequently, Haemoglobin High Pressure Liquid Chromatography (Hb HPLC) was done. His chromatogram showed raised HbF concentration (5.8%) and borderline/or reduced HbA2 concentration (3.1%). He was finally diagnosed as a case of HPFH trait. He was given folic acid and 250 mL of the whole blood transfusion during his stay in hospital. Pesticide and/or insecticide might have caused severe hypoplastic anaemia. Moreover, piperacillin and gentamicin might have also contributed to thrombocytopenia. Detection of HPFH trait appeared to be important for its prevention in our region.https://jcdr.net/articles/PDF/13546/43368_F(KM)_CE[Ra1]_(SL)_PF1(AG_SHU)_PN(SL).pdfhypoplastic anaemiapesticide exposurethrombocytopenia |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
AK Kapoor S Maurya Geeta |
spellingShingle |
AK Kapoor S Maurya Geeta Hypoplastic Bone Marrow Failure in a Patient with Hereditary Persistence of Foetal Haemoglobin (HPFH) Trait Journal of Clinical and Diagnostic Research hypoplastic anaemia pesticide exposure thrombocytopenia |
author_facet |
AK Kapoor S Maurya Geeta |
author_sort |
AK Kapoor |
title |
Hypoplastic Bone Marrow Failure in a Patient with Hereditary Persistence of Foetal Haemoglobin (HPFH) Trait |
title_short |
Hypoplastic Bone Marrow Failure in a Patient with Hereditary Persistence of Foetal Haemoglobin (HPFH) Trait |
title_full |
Hypoplastic Bone Marrow Failure in a Patient with Hereditary Persistence of Foetal Haemoglobin (HPFH) Trait |
title_fullStr |
Hypoplastic Bone Marrow Failure in a Patient with Hereditary Persistence of Foetal Haemoglobin (HPFH) Trait |
title_full_unstemmed |
Hypoplastic Bone Marrow Failure in a Patient with Hereditary Persistence of Foetal Haemoglobin (HPFH) Trait |
title_sort |
hypoplastic bone marrow failure in a patient with hereditary persistence of foetal haemoglobin (hpfh) trait |
publisher |
JCDR Research and Publications Private Limited |
series |
Journal of Clinical and Diagnostic Research |
issn |
2249-782X 0973-709X |
publishDate |
2020-03-01 |
description |
Hereditary Persistence of Foetal Haemoglobin (HPFH) trait is a rare genetic disorder and is caused by a large deletion involving δ and β globin genes. It is characterised by persistence of Foetal Haemoglobin (HbF) even in an adult. HbF level may vary from 2 to 30% in carriers of HPFH. Clinically, HPFH trait is asymptomatic without relevant haematological alterations. Mostly, HPFH trait is detected incidently while screening for other haemoglobinopathies. Herewith, we report a case of HPFH trait in our population. A 10-year-old boy born of non-consanguineous marriage complained of dyspnoea on exertion and dizziness. On examination he had generalised pallor. Earlier, he gave history of exposure to pesticides while spraying on crops. Later, he developed neutropenia (neutrophils 2000/mm3). He was immediately treated with piperacillin and gentamicin. Later, he was found to be severely anaemic (haemoglobin 3.0 gm/dL). His serum ferritin was within normal range. He also had severe thrombocytopenia (Platelets 10×109/L). Subsequently, Haemoglobin High Pressure Liquid Chromatography (Hb HPLC) was done. His chromatogram showed raised HbF concentration (5.8%) and borderline/or reduced HbA2 concentration (3.1%). He was finally diagnosed as a case of HPFH trait. He was given folic acid and 250 mL of the whole blood transfusion during his stay in hospital. Pesticide and/or insecticide might have caused severe hypoplastic anaemia. Moreover, piperacillin and gentamicin might have also contributed to thrombocytopenia. Detection of HPFH trait appeared to be important for its prevention in our region. |
topic |
hypoplastic anaemia pesticide exposure thrombocytopenia |
url |
https://jcdr.net/articles/PDF/13546/43368_F(KM)_CE[Ra1]_(SL)_PF1(AG_SHU)_PN(SL).pdf |
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