Lipaemic serum in Hb E-Beta thalassaemia major: A rare case of hypertriglyceridaemia thalassaemia syndrome.

Autor:	Mohd Kasim NA; UiTM, Faculty of Medicine, Department of Pathology, Department of Paediatrics & Department of Biochemistry & Molecular Medicine, Sungai Buloh,47000 Sungai Buloh, Selangor, Malaysia., Mohd Nor NS; UiTM, Faculty of Medicine, Department of Pathology, Department of Paediatrics & Department of Biochemistry & Molecular Medicine, Sungai Buloh,47000 Sungai Buloh, Selangor, Malaysia. shafinamohdnor@yahoo.com., Wen MT; Hospital Sungai Buloh, Department of Pathology & Department of Paediatric, 47000 Sungai Buloh, Selangor, Malaysia., Syed Kamaruddin SKA; Hospital Sungai Buloh, Department of Pathology & Department of Paediatric, 47000 Sungai Buloh, Selangor, Malaysia., Sheikh Abdul Kadir SH; UiTM, Faculty of Medicine, Department of Pathology, Department of Paediatrics & Department of Biochemistry & Molecular Medicine, Sungai Buloh,47000 Sungai Buloh, Selangor, Malaysia.
Jazyk:	angličtina
Zdroj:	The Malaysian journal of pathology [Malays J Pathol] 2023 Aug; Vol. 45 (2), pp. 293-296.
Abstrakt:	Introduction: A 1-year-old Malay girl presented with pallor, failure to thrive and hepatosplenomegaly. Her blood was sent for thalassaemia screening and it was incidentally found that her blood appeared lipaemic. Case Report: Primary and secondary causes of hyperlipidaemia were investigated. Her blood was sent for fasting lipid profile, thyroid function test (TFT), fasting plasma glucose (FPG), liver function test (LFT), renal profile (RP) and HIV screening. Lipaemic interference was removed by high-speed centrifugation. She is a product of non-consanguineous marriage. She is staying together with her stepfather who is HIV positive. Her mother's infective status was negative with no dyslipidaemic features and a normal lipid profile. Lipid profile of her biological father was not known. No other lipid stigmata such as eruptive xanthoma or lipaemia retinalis was seen in the patient. Haemoglobin analysis showed Hb E-Beta thalassaemia major. Her triglycerides was 9.05 mmol/L with normal total cholesterol, 2.85 mmol/L and high-density lipoprotein cholesterol (HDL-c), 0.26 mmol/L. Calculated low-density lipoprotein cholesterol (LDL-c) was invalid as triglycerides was >4.5 mmol/L. TFT, RP, FPG, LFT were normal and HIV status was negative. She was transfused with 10 ml/kg packed cell and her blood post transfusion appeared non lipaemic. Conclusion: Primary hypertriglyceridaemia was excluded based on insignificant family history of dyslipidaemia. Secondary causes of hypertriglyceridaemia were ruled out based on unremarkable laboratory investigations. Thus, we conclude that this patient is having hypertriglyceridaemia thalassaemia syndrome (HTS) which is a rare disorder with unknown pathogenesis. Further research may be required to explore this unknown association.
Databáze:	MEDLINE
Externí odkaz:	Zobrazit plný text záznamu