Vitamin B12 Deficiency and Hemoglobin H Disease Early Misdiagnosed as Thrombotic Thrombocytopenic Purpura: A Series of Unfortunate Events

Author:

Andreadis Panagiotis1,Theodoridou Stamatia2,Pasakiotou Marily3,Arapoglou Stergios4,Gigi Eleni1,Vetsiou Evaggelia1,Vlachaki Efthymia1

Affiliation:

1. Second Department of Internal Medicine, Aristotle University, Hippokration Hospital, 54642 Thessaloniki, Greece

2. Thalassemia Unit, Hippokration Hospital, 54642 Thessaloniki, Greece

3. Intensive Care Unit, Hippokration Hospital, 54642 Thessaloniki, Greece

4. Fifth Surgical Clinic, Aristotle University, Hippokration Hospital, 54642 Thessaloniki, Greece

Abstract

We herein would like to report an interesting case of a patient who presented with anemia and thrombocytopenia combined with high serum Lactic Dehydrogenase where Thrombotic Thrombocytopenic Purpura was originally considered. As indicated a central venous catheter was inserted in his subclavian vein which led to mediastinal hematoma and finally intubation and Intensive Care Unit (ICU) hospitalization. After further examination patient was finally diagnosed with B12 deficiency in a setting of H hemoglobinopathy. There have been previous reports where pernicious anemia was originally diagnosed and treated as Thrombotic Thrombocytopenic Purpura but there has been none to our knowledge that was implicated with hemothorax and ICU hospitalization or correlated with thalassemia and we discuss the significance of accurate diagnosis in order to avoid adverse reactions and therapy implications.

Publisher

Hindawi Limited

Subject

Cell Biology,Developmental Biology,Embryology,Anatomy

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