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急性淋巴细胞白血病初始阶段并发肾性尿崩症及单倍体造血干细胞移植后复发:一例报告

Nephrogenic diabetes insipidus in initial stage of acute lymphoblastic leukemia and relapse after haploidentical hematopoietic stem-cell transplantation: A case report.

作者信息

Li Dezhi, Liu Qian, Feng Zhifang, Zhang Qi, Feng Saran

机构信息

Department of Respiratory Medicine, Shandong Provincial Hospital Affiliated to Shandong University Department of Hematology, Shandong Provincial Qianfoshan Hospital, Jinan City Department of Endocrinology, Zhucheng Traditional Chinese Medicine Hospital, Zhucheng City, China Drug Discovery and Biomedical Sciences, College of Pharmacy, University of South Carolina, Columbia, SC.

出版信息

Medicine (Baltimore). 2018 Jun;97(24):e11157. doi: 10.1097/MD.0000000000011157.

Abstract

RATIONALE

Nephrogenic diabetes insipidus (NDI) rarely presents in the initial stage of acute lymphoblastic leukemia (ALL) and relapse due to renal infiltration is also rare.

PATIENT CONCERNS

A 19-year-old man presented with weakness, polydipsia, and polyuria for 1 month.

DIAGNOSES

NDI was diagnosed with insignificant response to a water deprivation test after stimulation with vasopressin injection. Bone marrow examination combined with immunophenotypic analysis, cerebrospinal cytology, and abdominal ultrasonography confirmed the diagnoses of precursor B cell ALL with renal infiltration.

INTERVENTIONS

The patient accepted standardized combination chemotherapy and ultimately had sustained remission, and his polydipsia and polyuria disappeared after 3 days of treatment. The ALL relapsed 1 year later and he received haploidentical stem cell transplantation (haplo-SCT) from his father.

OUTCOMES

One year later, he again developed NDI, with bilateral renal enlargement because of extramedullary relapse, leading to subsequent death.

LESSONS

This case demonstrates unusual early renal involvement in ALL presenting with initial NDI. Interestingly, the NDI returned with the relapse of renal infiltration 1 year after haplo-SCT. This case suggests that NDI was probably secondary to renal leukemic infiltration.

摘要

理论依据

肾性尿崩症(NDI)在急性淋巴细胞白血病(ALL)的初始阶段很少出现,并且由于肾浸润导致的复发也很少见。

患者情况

一名19岁男性出现乏力、烦渴和多尿1个月。

诊断

经血管加压素注射刺激后进行禁水试验,反应不明显,诊断为NDI。骨髓检查结合免疫表型分析、脑脊液细胞学检查和腹部超声检查确诊为前体B细胞ALL伴肾浸润。

干预措施

患者接受了标准化联合化疗,最终实现持续缓解,治疗3天后烦渴和多尿消失。1年后ALL复发,他接受了来自其父亲的单倍体干细胞移植(haplo-SCT)。

结果

1年后,他再次出现NDI,由于髓外复发导致双侧肾脏肿大,最终死亡。

经验教训

该病例显示ALL早期出现不寻常的肾脏受累,表现为初始NDI。有趣的是,单倍体干细胞移植1年后,随着肾浸润复发,NDI再次出现。该病例提示NDI可能继发于肾白血病浸润。

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