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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Main Authors: AK Kapoor, S Maurya, Geeta
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2020-03-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/13546/43368_F(KM)_CE[Ra1]_(SL)_PF1(AG_SHU)_PN(SL).pdf
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spelling 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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