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1.
Br J Haematol ; 202(6): 1192-1198, 2023 09.
Article in English | MEDLINE | ID: mdl-37438880

ABSTRACT

Sickle cell disease (SCD) is one of the most common monogenic disorders worldwide and liver complications are common in this group of patients. Our study aims to highlight the prevalence of chronic liver complications and the main predisposing factors for advanced liver fibrosis in SCD patients. For this purpose, 219 patients from eight Thalassemia and Sickle Cell Units across Greece enrolled in our study and history of liver related disease complications was recorded, as well as a full laboratory and imaging analysis concerning their liver function. 13.6% of the patients had advanced liver fibrosis. The presence of liver fibrosis was significantly correlated with advanced age, male gender, cholelithiasis and higher LDH, γ-GT, INR, direct and indirect bilirubin levels. These patients had exhibited significantly more episodes of liver crises and acute intrahepatic cholestasis. No correlation was observed with right heart failure or previous viral hepatitis. Patients with advanced liver fibrosis were receiving a more intensive transfusion therapy for a longer period of time and had higher Liver Iron Concentration levels. Our study shows that liver complications and cirrhosis is a significant cause of morbidity in patients with SCD and it is primarily associated with intravascular hemolysis and vaso-occlusive phenomena and secondarily with iron overload.


Subject(s)
Anemia, Sickle Cell , Liver Diseases , Humans , Male , Anemia, Sickle Cell/complications , Anemia, Sickle Cell/therapy , Liver Cirrhosis/etiology , Blood Transfusion/methods , Liver Diseases/complications , Liver
2.
Eur J Case Rep Intern Med ; 9(10): 003395, 2022.
Article in English | MEDLINE | ID: mdl-36415837

ABSTRACT

Intravesical bacillus Calmette-Guérin (BCG) instillation is widely used for the treatment of superficial bladder cancer. BCGitis is a serious immune-mediated complication with systematic manifestations and a high mortality rate. Here, we describe a case of a 64-year-old male patient who presented with haemophagocytic lymphohistiocytosis syndrome (HLH) after BCG instillation and was effectively treated with high-dose dexamethasone, intravenous immunoglobulins and anti-tuberculosis treatment. LEARNING POINTS: BCGitis after intravesical BCG instillation is a rare, but potentially fatal complication.HLH syndrome associated with BCGitis should be suspected in patients with systematic symptoms, cytopenias and elevated inflammation markers.Prompt diagnosis and early treatment is essential for reducing the mortality rates of this rare clinical entity.

3.
Hemoglobin ; 46(2): 114-117, 2022 Mar.
Article in English | MEDLINE | ID: mdl-36069257

ABSTRACT

Red blood cell (RBC) transfusions have been established as one of the primary therapies in treating sickle cell anemia. However, they are not free of side effects, with overloading the body with iron being one of the most important. Iron chelation therapy greatly reduces the iron load of the body. In addition, hydroxyurea (HU), an oral chemotherapeutic drug also has a significant role in the treatment of the disease with beneficial effects on many of the clinical problems that arise, mainly in reducing painful crises. The aim of this study was to investigate the effect of synergistic transfusion therapy and HU on the response to deferasirox (DFX) chelation therapy. Eighteen patients with sickle cell disease were divided into two groups based on their treatment, either with simple transfusions and DFX or with a combination of transfusion therapy, DFX and HU, and were evaluated with magnetic resonance imaging (MRI) for liver iron concentration (LIC) and biochemistry. All patients completed the study. The results of the study showed improvement in serum ferritin (FER) levels and LIC after 12 months of therapy in both groups, especially in the group receiving the combination therapy with HU. In addition, there was a noteworthy improvement in serum glutamic-oxaloacetic transaminase (SGOT), serum glutamic pyruvic transaminase (SGPT) and lactate dehydrogenase (LDH) levels with serum creatinine (Cr) levels remaining stable during the study in both groups. Hydroxyurea, when combined with iron chelators such as DFX, provides an additional benefit of iron chelation in patients receiving chronic transfusion therapy.


Subject(s)
Anemia, Sickle Cell , Iron Chelating Agents , Iron Overload , Alanine Transaminase/therapeutic use , Anemia, Sickle Cell/complications , Anemia, Sickle Cell/therapy , Aspartate Aminotransferases/therapeutic use , Chelation Therapy , Creatinine/therapeutic use , Deferasirox/therapeutic use , Ferritins , Humans , Hydroxyurea/therapeutic use , Iron , Iron Chelating Agents/therapeutic use , Iron Overload/drug therapy , Iron Overload/etiology , Lactate Dehydrogenases
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