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噬血细胞性淋巴组织细胞增生症继发于幼年粒单核细胞白血病:病例报告及文献复习。

Hemophagocytic Lymphohistiocytosis Secondary to Juvenile Myelomonocytic Leukemia: A Case Report and Review of the Literature.

机构信息

Department of Pediatrics, Peking University People's Hospital, Beijing, China.

出版信息

J Pediatr Hematol Oncol. 2022 Mar 1;44(2):e580-e584. doi: 10.1097/MPH.0000000000002273.

Abstract

RATIONALE

Juvenile myelomonocytic leukemia (JMML) is a rare hematopoietic disorder, which is more rarely accompanied by monosomy 5 or deletion of the long arm of chromosome 5q (-5/5q-) or monosomy 5 (5q-/-5), and hemophagocytic lymphohistiocytosis (HLH) is a rare, uncontrolled hyperinflammation condition, which is more rarely secondary to JMML. Up to now, only a few cases of JMML with -5/5q- and HLH secondary to JMML were described. Here we described an extremely rare case of HLH second to JMML with 5q-.

PATIENT CONCERNS

The patient had multiple cafe-au-lait-spots at birth and was found that NF1 gene mutation was positive. At his 6 years old, he developed hepatosplenomegaly, anemia, thrombocytopenia, monocyte count 4.12×109/L in peripheral blood, 13% blasts in peripheral blood, and 11% blasts in bone marrow, without BCR/ABL rearrangement, combining with positive NF1 gene mutation, he was diagnosed as JMML. In the bone marrow, there was chromosomal abnormalities with -5/5q-. In the treatment, HLH occurred.

DIAGNOSES

The patient was diagnosed as secondary HLH to JMML.

INTERVENTIONS

The patient received the chemotherapy treatment of the improved diffuse alveolar hemorrhage protocol, and meanwhile, he prepared for hematopoietic stem cell transplantation. Then on the basis of anti-infection, symptomatic and supportive therapy, he was commenced the treatment according to the HLH-2004 protocol.

OUTCOMES

He had a partial response, manifesting that his fever resolved, but the blood coagulation function did not improve, and the severe thrombocytopenia remained. Then, the parents refused the continual treatment, and the child died of intracranial hemorrhage 3 months after the diagnosis of JMML.

LESSONS

JMML and HLH were relatively easy to diagnose based on clinical and laboratory results. Due to the low incidence of JMML with -5/5q- and HLH secondary to JMML, no clinical practice guidelines for the treatment of the disease have been established yet. The clinical data of a case of HLH secondary to JMML with 5q- were analyzed, and relevant studies were studied.

摘要

背景

幼年髓单核细胞白血病(JMML)是一种罕见的造血系统疾病,较少伴有单体 5 或 5 号染色体长臂缺失(-5/5q-)或单体 5(5q-/-5),噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见的、失控性的过度炎症状态,较少继发于 JMML。迄今为止,仅描述了少数 JMML 伴-5/5q-和继发于 JMML 的 HLH 病例。在此,我们描述了一例极其罕见的继发于 JMML 的 HLH 伴 5q-病例。

病例描述

患儿出生时即有多发性咖啡牛奶斑,且发现 NF1 基因突变阳性。6 岁时出现肝脾肿大、贫血、血小板减少,外周血单核细胞计数为 4.12×109/L,外周血中存在 13%的原始细胞,骨髓中存在 11%的原始细胞,无 BCR/ABL 重排,结合 NF1 基因突变阳性,诊断为 JMML。骨髓中存在染色体异常,为-5/5q-。在治疗过程中出现 HLH。

诊断

患者诊断为继发于 JMML 的 HLH。

干预措施

患者接受了改良弥漫性肺泡出血方案的化疗治疗,同时准备进行造血干细胞移植。在此基础上,给予抗感染、对症支持治疗,并根据 HLH-2004 方案开始治疗。

结果

患者部分缓解,表现为发热缓解,但凝血功能未改善,严重血小板减少仍持续存在。随后,患儿父母拒绝继续治疗,患儿在诊断为 JMML 后 3 个月因颅内出血死亡。

教训

根据临床和实验室结果,JMML 和 HLH 相对容易诊断。由于 JMML 伴-5/5q-和继发于 JMML 的 HLH 发病率较低,尚未制定针对该疾病的治疗临床实践指南。我们分析了一例继发于 JMML 的 HLH 伴 5q-的临床资料,并对相关研究进行了研究。

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