Agranulocytosis in systemic lupus erythematosus: A case report

Abstract

Abstract 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