Sarkar R N, Banerjee S, Dey S, Saha A, Bhattacharjee P, Banerjee T K, Sinha P K, Chakraborty A
Department of Medicine, Head, Division of Rheumatology, Medical College & Hospital, Kolkata.
J Assoc Physicians India. 2009 Nov;57:767-8.
Haematological manifestations are quite common in systemic lupus erythematosus (SLE) but bone marrow aplasia and secondary myelofibrosis are rare manifestations. We report a case of 45 years old male patient who presented with fever, malaena and anaemia without any clinical features of SLE. He had patches of vitiligo for 25 years for which he was applying psoralen with sunlight exposure. This probably precipitated SLE in this patient. The patient presented with pancytopenia which was due to a combination of Comb's positive haemolytic anaemia and myelofibrosis.
血液学表现在系统性红斑狼疮(SLE)中相当常见,但骨髓再生障碍和继发性骨髓纤维化是罕见表现。我们报告一例45岁男性患者,其表现为发热、黑便和贫血,无任何SLE的临床特征。他有25年的白癜风斑块,为此他一直在使用补骨脂素并接受阳光照射。这可能促使该患者发生了SLE。该患者出现全血细胞减少,这是由抗人球蛋白试验阳性的溶血性贫血和骨髓纤维化共同所致。