Excellent response of severe aplastic anemia to treatment of gut inflammation: A case report and review of the literature

被引:1
作者
Zhao, Xi-Chen [1 ]
Zhao, Li [1 ]
Sun, Xiao-Yun [1 ]
Xu, Zeng-Shan [1 ]
Ju, Bo [1 ]
Meng, Fan-Jun [2 ]
Zhao, Hong-Guo [2 ]
机构
[1] Cent Hosp Qingdao West Coast New Area, Dept Hematol, Qingdao 266555, Shandong, Peoples R China
[2] Qingdao Univ, Dept Hematol, Affiliated Hosp, 16 Jiangsu Rd, Qingdao 266000, Shandong, Peoples R China
关键词
Case report; Severe aplastic anemia; Hematological response; Chronic gut inflammation; Comorbid disease; Etiological association; ULCERATIVE-COLITIS; CELIAC-DISEASE; T-CELLS; NEUTROPENIC ENTEROCOLITIS; MICROBIOTA; AZATHIOPRINE; ASSOCIATION; GLOBULIN; SAFETY;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Cumulative evidence suggests that the aberrant immune responses in acquired aplastic anemia (AA) are sustained by active chronic infections in genetically susceptible individuals. Recently, the constant source to trigger and sustain the pathophysiology has been proposed to come from the altered gut microbiota and chronic intestinal inflammation. In this case, our serendipitous finding provides convincing evidence that the persistently dysregulated autoimmunity may be generated, at least in a significant proposition of AA patients, by the altered gut microbiota and compromised intestinal epithelium. CASE SUMMARY A 30-year-old Chinese male patient with refractory severe AA experienced a 3-month-long febrile episode, and his fever was refractory to many kinds of injected broad-spectrum antibiotics. When presenting with abdominal cramps, he was prescribed oral mannitol and gentamycin to get rid of the gut infection. This treatment resulted in a quick resolution of the fever. Unanticipatedly, it also produced an excellent hematological response. He had undergone three episodes of recurrence within the one-year treatment, with each recurrence occurring 7-8 wk from the gastrointestinal inflammation eliminating preparations. However, subsequent treatments were able to produce subsequent remissions and consecutive treatments were successful in achieving durative hematological improvements, strongly indicating an etiological association between chronic gut inflammation and the development of AA. Interestingly, comorbid diseases superimposed on this patient (namely, psychiatric disorders, hypertension, insulin resistance, and renal dysfunction) were ameliorated together with the hematological improvements. CONCLUSION Chronic gut inflammation may be responsible for AA pathogenesis. The comorbidities and AA may share a common etiological association.
引用
收藏
页码:425 / 435
页数:11
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