Erythrophagocytosis by Neutrophils in Paroxysmal Cold Hemoglobinuria

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Ann Hematol Oncol. 2017; 4(5): 1151.

Erythrophagocytosis by Neutrophils in Paroxysmal Cold Hemoglobinuria

Sampagar A¹, Bartakke S²*, Lukade U³ and Sethuratnam S³

¹Department of Pediatrics, Jawaharlal Nehru Medical College and Hospital, India

¹Department of Clinical Hematology, Aditya Birla Memorial Hospital, India

³Department of Pathology, Aditya Birla Memorial Hospital, India

*Corresponding author: Sandip Bartakke, Department of Clinical Hematology, Aditya Birla Memorial Hospital, Pune, India

Received: April 12, 2017; Accepted: April 27, 2017; Published: May 17, 2017

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Paroxysmal Cold Hemoglobinuria (PCH) is the most common cause of acute autoimmune hemolytic anaemia in children [1,2]. The presence of marked erythrophagocytosis by neutrophils is a relatively rare observation on blood smears, but it is a prominent feature of PCH [3-5]. This case highlights the necessity for clinicians to be aware of the importance of erythrophagocytosis in diagnosis of PCH.

A 4-year-old boy presented with 4 days history of fever, jaundice and dark colored urine. On examination, he had pallor and icterus. A complete blood count was remarkable for haemoglobin of 41 gm/l, a white cell count of 27.1 x109/l and a platelet count of 367x109/l. The reticulocyte count was 2%. Serum lactate dehydrogenase was significantly elevated at 4700 U/L. His serum creatinine was 2.0 mg/ dl and urine analysis showed presence of hemoglobin.