Mendiola Vincent Louie, Qian You-Wen, Jana Bagi
Department of Internal Medicine, University of Texas Medical Branch, Galveston, Texas, USA.
Department of Pathology, University of Texas Medical Branch, Galveston, Texas, USA.
Case Rep Oncol. 2018 Dec 20;11(3):871-879. doi: 10.1159/000495458. eCollection 2018 Sep-Dec.
Chronic neutrophilic leukemia (CNL) is an extremely rare myeloproliferative neoplasm (MPN). Due to the difficulty in its diagnosis, the diagnostic criterion was just recently revised in 2016. CNL is defined as: A clonal disorder with sustained primary neutrophilia, with normal neutrophil maturation, that does not meet other MPN criteria, as well as no identifiable mutations of the PDGFRA, PDGFRB or FGFR1 or PCM1-JAK2 genes, and, either, the presence of a CSF3R mutation, or if absent, the presence of sustained neutrophilia (> 3 months), splenomegaly and no other identifiable cause of reactive neutrophilia including the absence of a plasma cell neoplasm, or, if present, demonstration of myeloid cell clonality by cytogenetics. Only about 200 cases have been reported.
We report a 61-year-old Caucasian male patient who initially presented with unexplained leukocytosis. An outpatient work-up was planned to rule out a myeloproliferative disorder but the patient was acutely admitted for MRSA septic shock. The patient was stabilized prior bone marrow work-up and was then diagnosed with an atypical type of CNL (JAK2 positive, CSF3R negative). The patient refused further treatment due to social circumstances and requested palliative care instead.
This case aims to present atypical findings of an extremely rare MPN. Even though a recent revision has been made to help in its diagnosis, atypical findings must still be considered. This, in turn, will help to further improve the current CNL diagnostic criteria.
慢性中性粒细胞白血病(CNL)是一种极其罕见的骨髓增殖性肿瘤(MPN)。由于其诊断困难,诊断标准于2016年才刚刚修订。CNL的定义为:一种具有持续性原发性中性粒细胞增多、中性粒细胞成熟正常的克隆性疾病,不符合其他MPN标准,且不存在PDGFRA、PDGFRB或FGFR1或PCM1-JAK2基因的可识别突变,并且,要么存在CSF3R突变,要么在不存在该突变的情况下,存在持续性中性粒细胞增多(>3个月)、脾肿大且无其他可识别的反应性中性粒细胞增多原因,包括不存在浆细胞肿瘤,或者,如果存在浆细胞肿瘤,则通过细胞遗传学证明髓系细胞克隆性。仅报道了约200例病例。
我们报告一名61岁的白种男性患者,最初表现为不明原因的白细胞增多。计划进行门诊检查以排除骨髓增殖性疾病,但患者因耐甲氧西林金黄色葡萄球菌败血症休克而紧急入院。患者在进行骨髓检查之前病情稳定,随后被诊断为非典型类型的CNL(JAK2阳性,CSF3R阴性)。由于社会情况,患者拒绝进一步治疗,而是要求姑息治疗。
本病例旨在呈现一种极其罕见的MPN的非典型表现。尽管最近进行了修订以帮助诊断,但仍必须考虑非典型表现。这反过来将有助于进一步完善当前的CNL诊断标准。