“…ES has been described in several medical conditions including: (10) plasma cell disorders such as multiple myeloma, amyloidosis, POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein and skin changes) and plasma cell leukemia; (2) leukemias including: acute myeloid leukemia, acute lymphoblastic leukemia, chronic myeloid leukemia (CML) and chronic lymphocytic leukemia; (3) lymphomas, mainly non-Hodgkin types; (4) solid tumors such as breast cancer; and (5) autoimmune disorders such as multiple sclerosis [1,3,10,11,16,22]. In addition to the forms of HSCT and the types of medical illnesses described above, additional risk factors for the development of ES include: (1) female gender, (2) older age, (3) absence of previous chemotherapy or the use of less aggressive chemotherapeutic agents prior to HSCT, (4) use of busulfan, cyclophosphamide, fludarabine and etoposide, (5) The clinical manifestations of ES include: (1) common and characteristic features that include: non-infectious fever; skin rash; PERDS manifested as pulmonary edema, lung infiltrates and hypoxemia; diarrhea; weight gain; renal dysfunction; hepatic dysfunction with jaundice; transient encephalopathy; and capillary leak syndrome manifesting as: weight gain, edema, ascites as well as hypoalbuminemia; and (2) rarely described manifestations which include: severe colitis, pericarditis, acute brachial neuropathy in addition to bilateral marginal keratitis [1][2][3][8][9][10][11]18,24,[27][28][29][30]. The diagnostic criteria for ES are included in Table 1 [1-3,10,11].…”