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通过胸腔积液的数字化细胞分析诊断T系急性淋巴细胞白血病。

Diagnosis of a T-lineage acute lymphoblastic leukemia through digitalized cell analysis of the pleural effusion.

作者信息

Peruzzi Benedetta, Cutini Ilaria, Gelli Anna Maria Grazia, Rondelli Tommaso, Statello Marinella, Bencini Sara, Mannelli Francesco, Caporale Roberto, Bosi Alberto, Fanelli Alessandra

机构信息

General Laboratory Unit (Microscopy and Clinical Cytometry Unit), Firenze, Italy.

出版信息

Int Med Case Rep J. 2013 Nov 1;6:77-80. doi: 10.2147/IMCRJ.S49278. eCollection 2013.

Abstract

INTRODUCTION

Pleural effusion as the first clinical manifestation of acute lymphoblastic leukemia (ALL) is a relatively rare event. An early and accurate diagnosis of this clinical picture is very important for adequate patient management.

CASE PRESENTATION

We report the atypical onset of T-lineage ALL in a 31-year-old man. The patient was admitted to the emergency room due to lung failure; at that moment, the patient's initial blood count was normal; the chest X-ray radiography showed a massive pleural effusion and a thoracentesis was carried out. Routine investigations performed on the pleural fluid using a new technology system and digitalized cell analysis demonstrated infiltration by immature cells. Therefore, bone marrow aspirate and flow cytometry analyses were performed, leading to the diagnosis of T-lineage ALL. A cord blood transplantation procedure was performed at the first hematological remission following chemotherapy regimens. The patient died of septic shock.

CONCLUSION

The case we reported underlines the usefulness of using automated instruments to identify abnormal lymphoid cells in body fluids.

摘要

引言

胸腔积液作为急性淋巴细胞白血病(ALL)的首发临床表现相对罕见。对这种临床情况进行早期准确诊断对于患者的恰当管理非常重要。

病例报告

我们报告了一名31岁男性T系急性淋巴细胞白血病的非典型发病情况。该患者因呼吸衰竭入住急诊室;当时患者的初始血常规正常;胸部X线摄影显示大量胸腔积液,遂进行了胸腔穿刺术。使用新技术系统和数字化细胞分析对胸腔积液进行的常规检查显示有未成熟细胞浸润。因此,进行了骨髓穿刺和流式细胞术分析,从而诊断为T系急性淋巴细胞白血病。在化疗方案后的首次血液学缓解期进行了脐血移植手术。患者死于感染性休克。

结论

我们报告的病例强调了使用自动化仪器识别体液中异常淋巴细胞的有用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/205f/3818024/897446ffe6f3/imcrj-6-077Fig1.jpg

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