%0 Journal Article
%T A Case Report of Hairy Cell Leukemia Presenting Concomitantly with Sweet Syndrome
%A Mohammad Alkayem
%A Waina Cheng
%J Case Reports in Medicine
%D 2014
%I Hindawi Publishing Corporation
%R 10.1155/2014/823286
%X Hairy cell leukemia and Sweet syndrome are both uncommon hematological diagnoses. We present a patient who was admitted with fevers, pancytopenia, pneumonia, and rash. Diagnostic bone marrow biopsy demonstrates Hairy cell Leukemia and skin biopsy demonstrates neutrophils infiltration consistent with Sweet syndrome. The patient was treated with purine analogs with resolution of the cytopenias, infection, and rash. 1. Introduction Hairy cell leukemia is an uncommon lymphoproliferative disorder often presenting with cytopenias, infections, and splenomegaly. In this case report, we will discuss a presentation of hairy cell leukemia with Sweet syndrome. 2. Case Report A-52-year-old male presented to Lincoln Medical and Mental Health Center in March 2012 with fever, chills, dyspnea, and productive cough for 3 days. The physical exam was significant for tachycardia, tachypnea, fever of 102¡ãF, and fine crackles heard in the right side of the chest. The patient¡¯s CBC showed neutropenia with ANC 900, mild anemia with hemoglobin 12.2£¿g/dL, and thrombocytopenia with platelets 79 ¡Á 103. Initial blood smear demonstrated a limited number of white blood cells. A chest X-ray revealed right lower lobe consolidation. Computerized tomography (CT) scan of chest and abdomen revealed enlargement of the mediastinal lymph nodes and a mildly enlarged spleen. Within 24 hours of admission, the patient went into respiratory failure requiring ventilator support. He was subsequently placed on antibiotics for community acquired pneumonia with improvement in symptoms. On the 3rd day of hospitalization, physical exam was notable for development of a generalized erythematous papular rash on the abdomen and vesicles and bullae on the extremities. A punch skin biopsy was performed and the patient was started on systemic steroids with improvement of the rash. One week later, despite clinical improvement, patient had persistent pancytopenia. A diagnostic bone marrow biopsy was performed. No aspirate was able to be obtained despite multiple attempts. Bone marrow core biopsy show large lymphocytes with small cytoplasmic projections (Figure 1). The neoplastic cells stained positive for CD45, CD19, CD20, CD11c, CD22, CD25, and CD103, consistent with hairy cell leukemia. Concurrently, the skin biopsy showed neutrophilic dermatosis, consistent with Sweet syndrome (Figure 2). Figure 1: Bone marrow biopsy showed infiltration with hairy cells. Figure 2: Infiltration with neutrophils (Sweet syndrome). Given resolution of his pneumonia, the patient received cladribine 0.1£¿mg/kg intravenous continuous
%U http://www.hindawi.com/journals/crim/2014/823286/