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血清总类胰蛋白酶水平证实自身是肥大细胞白血病(无白血病变异型)中肥大细胞负荷更可靠的标志物。

Serum total tryptase level confirms itself as a more reliable marker of mast cells burden in mast cell leukaemia (aleukaemic variant).

作者信息

Savini P, Rondoni M, Poletti G, Lanzi A, Quercia O, Soverini S, De Benedittis C, Musardo G, Martinelli G, Stefanini G F

机构信息

Department of Internal Medicine, Faenza Hospital, Viale Stradone 9, 48018 Faenza, Italy.

Department of Clinical Pathology, Centro Servizi Pievesestina, AUSL Romagna, Piazzale della Liberazione 60, Pievesestina, 47522 Cesena, Italy.

出版信息

Case Rep Hematol. 2015;2015:737302. doi: 10.1155/2015/737302. Epub 2015 Feb 10.

DOI:10.1155/2015/737302
PMID:25755899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4338389/
Abstract

Mast cell leukemia (MCL) is a very rare form of systemic mastocytosis (SM) with a short median survival of 6 months. We describe a case of a 65-year-old woman with aleukaemic variant of MCL with a very high serum total tryptase level of 2255 μg/L at diagnosis, which occurred following an episode of hypotensive shock. She fulfilled the diagnostic criteria of SM, with a bone marrow smear infiltration of 50-60% of atypical mast cells (MCs). She tested negative for the KIT D816V mutation, without any sign of organ damage (no B- or C-findings) and only few mediator-related symptoms. She was treated with antihistamine alone and then with imatinib for the appearance of anemia. She maintained stable tryptase level and a very indolent clinical course for twenty-two months; then, she suddenly progressed to acute MCL with a serum tryptase level up to 12960 μg/L. The patient died due to haemorrhagic diathesis twenty-four months after diagnosis. This clinical case maybe represents an example of the chronic form of mast cell leukemia, described as unpredictable disease, in which the serum total tryptase level has confirmed itself as a reliable marker of mast cells burden regardless of the presence of other signs or symptoms.

摘要

肥大细胞白血病(MCL)是系统性肥大细胞增多症(SM)的一种非常罕见的形式,中位生存期短,为6个月。我们描述了一例65岁女性患无白血病变异型MCL的病例,诊断时血清总类胰蛋白酶水平非常高,达2255μg/L,这发生在一次低血压休克发作之后。她符合SM的诊断标准,骨髓涂片中有50%-60%的非典型肥大细胞浸润。她的KIT D816V突变检测为阴性,没有任何器官损害迹象(无B级或C级发现),仅有少数与介质相关的症状。她先单独接受抗组胺药治疗,之后因出现贫血接受伊马替尼治疗。她的类胰蛋白酶水平保持稳定,临床病程非常惰性,持续了22个月;然后,她突然进展为急性MCL,血清类胰蛋白酶水平高达12960μg/L。患者在诊断后24个月因出血素质死亡。该临床病例可能代表了肥大细胞白血病慢性形式的一个例子,这种疾病被描述为不可预测,其中血清总类胰蛋白酶水平已证实是肥大细胞负荷的可靠标志物,而与其他体征或症状的存在无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a3/4338389/e8766ab126f7/CRIHEM2015-737302.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a3/4338389/575b0eeec383/CRIHEM2015-737302.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a3/4338389/e8766ab126f7/CRIHEM2015-737302.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a3/4338389/575b0eeec383/CRIHEM2015-737302.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a3/4338389/e8766ab126f7/CRIHEM2015-737302.002.jpg

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