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Sweet syndrome (SS) was described over 50 years ago as a distinctive form of neutrophilic dermatosis. It may be idiopathic, drug‐induced or paraneoplastic, and in the last of those subtypes, myeloproliferative diseases are prominently represented. A peculiar variant of SS is termed ‘histiocytoid’ SS (HSS), and early accounts of that condition asserted that it showed no linkage to hematological disorders...
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