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DOI 10.3389/fimmu.2024.1396260

Медицинская библиотека · Frontiers in immunology · 2024

Encephalitozoon hellem infection after haploidentical allogeneic hematopoietic stem cell transplantation in children: a case report.

Shang Yue, Ren Yuanyuan, Liu Lipeng, Chen Xia, Liu Fang, Li Xiaolan, Wan Yang, An Wenbin, Yang Wenyu, Zhu Xiaofan, Guo Ye

Клинический случайСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Encephalitozoon hellem (E. hellem) infection is a zoonotic disease, rarely observed in individuals, causing various clinical manifestations including diarrhea, keratoconjunctivitis, cystitis, etc. E. hellem infection after hematopoietic stem-cell transplantation (HSCT) is a rare, serious complication.

CASE PRESENTATION: Herein, we present a case of E. hellem infection developing during HLA-haploidentical HSCT in a 9-year-old boy who suffered from aplastic anemia. On 15 days after HSCT, the patient developed recurrent and prolonged fever, diarrhea and hematuria. It is challenging to differentiate whether the symptoms mentioned in this case are caused by graft-versus-host disease (GVHD) or a specific infection. Based on the result of metagenomic next-generation sequencing (mNGS) and clinical observation, the patient was diagnosed as E. hellem infection, and received albendazole and decreased the immunosuppressive treatment. Finally, he had recovered.

CONCLUSION

We should pay attention to the uncommon disease caused by the E. hellem infection after HSCT, especially in cases with immune reconstitution unrecovered. Among those rare infection, mNGS can be performed for better understanding the source of infection and targeted therapy, which can benefit the patients.

Для цитирования: Shang Yue, Ren Yuanyuan, Liu Lipeng, Chen Xia, Liu Fang, Li Xiaolan, Wan Yang, An Wenbin, Yang Wenyu, Zhu Xiaofan, Guo Ye. Encephalitozoon hellem infection after haploidentical allogeneic hematopoietic stem cell transplantation in children: a case report.. Frontiers in immunology. 2024. DOI: 10.3389/fimmu.2024.1396260.

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