Agranulocytosis is a rare acute condition characterized by severe a < gft (neutropenia in which the neutrophils count is less than 100/mm3. It can be classified into two categories, inherited, and acquired. Acquired agranulocytosis is not commonly caused by auto-immune diseases such as systemic lupus erythematosus (SLE). We report a case of a patient suffering from agranulocytosis related to SLE at disease onset, associated with other rare disease involvements.
Keywords: agranulocytosis; and acute pancreatitis; enteritis; pancytopenia; polyarthritis; pulmonary arterial hypertension; systemic lupus erythematosus.
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