罕见的aCML伴中枢神经系统受累及侵袭性临床病程

IF 0.7 Q4 HEMATOLOGY Leukemia Research Reports Pub Date : 2023-01-01 DOI:10.1016/j.lrr.2023.100361
Dorela Lame, Michelangelo Pianelli, Erika Morsia, Alberto Carturan, Gaia Goteri, Stefania Mancini, Attilio Olivieri, Antonella Poloni
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引用次数: 1

摘要

中性粒细胞增多症的存在可能是多种疾病的基础。一些罕见的中性粒细胞增多的原因可能是慢性中性粒细胞白血病(CNL)和骨髓增生异常/骨髓增生性肿瘤伴中性粒细胞增多(MDS伴中性粒细胞增多)。我们在此报告一位78岁的妇女,在常规检查中因严重的白细胞增多和贫血而来到我们的急诊室。患者无症状,最后一次检查显示轻度白细胞减少和血小板减少。腹部超声显示轻度脾肿大,患者行骨髓检查。一周后,病人出现精神恶化。患者行颅脑CT及RMN检查,发现脑实质、小脑及脑干多发11 mm病灶。一周后,临床表现恶化:患者处于昏迷状态,发烧40°C,对类固醇治疗无反应。尸检显示多个器官有白血病和出血浸润,骨髓细胞100%为髓细胞,成熟缓慢,母细胞5%。根据WHO 2016,该病例可报告为aCML,这是一种MDS/MPN重叠综合征,难以与CNL区分。
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A rare case of aCML associated with CNS involvement and with aggressive clinical course

The presence of neutrophilic leukocytosis may underlie a wide variety of diseases. Some rare causes of neutrophilia might be chronic neutrophilic leukemia (CNL) and myelodysplastic/myeloproliferative neoplasm with neutrophilia (MDS with neutrophilia). Here we report a case of a 78-year-old woman who came to our ER due to severe leukocytosis and anemia on a routine check-up. The patient was asymptomatic and the last exams available showed a mild leukopenia and thrombocytopenia. The abdominal echography showed mild splenomegaly The patient underwent bone marrow (BM) examinations. One week later, the patient presented mental deterioration. The patient underwent a cranial CT and RMN that showed multiple lesions of 11 mm in the brain parenchyma, cerebellum and encephalic trunk. Another week later, the clinical presentations worsened: she was in a comatous state and feverish 40 °C unresponsive to steroid therapy. Autopsy showed a leukemic and hemorrhage infiltration in multiple organs and in the BM a cellularity of 100% represented by myeloid elements with a slowdown maturation with blasts 5%. According to WHO 2016 this case can be reported as an aCML, an MDS/MPN overlap syndrome that is difficult to differentiate from a CNL.

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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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