“…The resemblance of so-called atypical or bullous pyoderma gangraenosum to Sweet's syndrome [17][18][19][20] was noted in the discussion by Pegum [21J after presentation of a patient labeled as having 'bullous pyoderma gangraenosum' and chronic myeloid leukemia. These neutrophilic dermatoses are pail of the same spectrum, often without fever or neu trophilia, hence the unifying name AND -as the histologic pattern in these patients consistently displays an extensive diffuse dermal infiltrate of neutrophils often with leukocytoclasia 11,3], There have been over 60 patients reported with AND and myeloproliferative disease [6, 13-16, 22, 23]; the latter was usually detected months after the onset of the skin changes, although in some patients they were detected simultaneously [2,22]; a few patients with AND have been first observed after the malignant diagnosis was established. The course of the skin lesions has been noted to parallel the leukemia, with the original observation of the rapid demise of the patient occurring in most cases so far reported, usually from myelogenous leukemia [19,24], AND has also been reported in association with myeloma, T-cell lymphoma, histiocytic lymphoma and over 40 solid tumors [1, 2, 13-15, 24-27], These solid tumors include carci noma of the ovary, testes, breast, uterus, stomach, vagina, colon, prostate, rectum, kidney and thyroid [13-15, 25, 27], Extracutaneous manifestations of Sweet's syndrome are varied.…”