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A case of ischemic colitis in a patient with non transfusion dependent thalassemia (NTDT) infected by SARS-COV-2

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Non transfusion dependent thalassemia (NTDT) are a wide spectrum of genetic diseases characterized by anemia, ineffective erythropoiesis and hemolysis which require blood transfusion supplies only in particular conditions such as… Click to show full abstract

Non transfusion dependent thalassemia (NTDT) are a wide spectrum of genetic diseases characterized by anemia, ineffective erythropoiesis and hemolysis which require blood transfusion supplies only in particular conditions such as pregnancy, infections and trauma. Here we present a case of ischemic colitis (IC) in a patient with NTDT following Coronavirus disease 2019 caused by SARS-COV-2 infection. EP is a 41-year-old male patient attending to our Thalassemia Unit since he was 4 years old when he received also his first blood transfusion. He was found to be heterozygous for b0 39 nonsense C!T mutation along with the db-thalassemia allele with a baseline hemoglobin almost completely (97%) represented by HbF. He has a severe/high risk form of NTDT. He was regularly transfused from 4 to 14 years old. Splenectomy was performed when he was 15 years old; thereafter, he received occasional transfusions only in case of infections. His baseline hemoglobin was about 8.2–8.9 g/dL. In 2004, to relieve anemia and stop the progression of extramedullary erythropoietic masses previously diagnosed, the patient was started on hydroxyurea (HU) therapy. His hemoglobin increased by approximately 1.5 g/dL, but despite HU treatment, platelet and nucleated red blood cell (NRBC) count still were high (650-750 10/L and 600-800 10/L, respectively) and therefore was under prophylactic anti-thrombotic therapy with ASA at dose of 100mg/die. Presently, he shows level of soluble transferrin receptor (sTfR) equal to 12mg/L and is affected by osteoporosis and hypothyroidism and is under thyroid hormone replacement therapy; he has a negative genetic thrombophilia profile and a negative family history for thrombosis. On 15 October 2020, the patient reported to suffer from fever, pharyngodynia, dry cough and headaches, and was able to breathe normally without oxygen. A nasopharyngeal swab for SARS-COV-2 RT-PCR was positive and therefore he was started on clarithromycin 500mg bis in die and prednisone 25mg/die for 7 days and then dose reduction. He was since a week afebrile and anosmic, without cough and headaches, when suddenly started to suffer from abdominal spasmodic pain, vomiting and hematochezia. On day 17 after first symptoms of SARS-COV-2, he presented to emergency department because of the worsening of gastrointestinal symptoms. The SARS-CoV-2 qualitative serology (IgG/IGM) and the nasopharyngeal swab were both positive. His hemoglobin was 9.4 g/dL (13.5–17.5 g/dL), and the mean corpuscular volume (MCV) was 84.2 fL (82–97 fL). White cell counts showed leucocytosis 29.43 10/lL (4.5–10 10/ lL), but NRBC count was within his historical range (730 10/L); lactate dehydrogenase

Keywords: thalassemia; case; non transfusion; sars cov; patient

Journal Title: Pediatric Hematology and Oncology
Year Published: 2021

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