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病例报告:髓外急性早幼粒细胞白血病:1例罕见病例及文献综述

Case Report: Extramedullary Acute Promyelocytic Leukemia: An Unusual Case and Mini-Review of the Literature.

作者信息

Harrer Dennis Christoph, Lüke Florian, Einspieler Ingo, Menhart Karin, Hellwig Dirk, Utpatel Kirsten, Herr Wolfgang, Reichle Albrecht, Heudobler Daniel

机构信息

Department of Internal Medicine III, Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.

Institute of Radiology, University Hospital Regensburg, Regensburg, Germany.

出版信息

Front Oncol. 2022 May 25;12:886436. doi: 10.3389/fonc.2022.886436. eCollection 2022.

Abstract

BACKGROUND

Acute promyelocytic leukemia (APL) constitutes a serious hematological emergency necessitating rapid diagnosis and therapy to prevent lethal bleedings resulting from APL-induced thrombocytopenia and coagulopathy. Atypical manifestations of APL, such as extramedullary disease at first presentation, pose diagnostic challenges and delay the onset of appropriate therapy. Nevertheless, extramedullary manifestations of APL are mostly accompanied by blood count alterations pointing to an underlying hematological disease. In this report, we present the first case of APL bearing close resemblance to a metastasized laryngeal carcinoma with normal blood counts and absent coagulopathy.

CASE PRESENTATION

A 67-year-old man with a previous history of smoking was admitted to our hospital with progressive hoarseness of voice, odynophagia, dysphagia and exertional dyspnea. Laryngoscopy revealed a fixed right hemi larynx with an immobile right vocal fold. Imaging of the neck magnetic-resonance imaging (MRI) and positron emission tomography-computed tomography (PET/CT) with F-18-fluordeoxyglucose (FDG) showed a large hypermetabolic tumor in the right piriform sinus and tracer uptake in adjacent lymph nodes, highly suspicious of metastasized laryngeal carcinoma. Surprisingly the histological examination revealed an extramedullary manifestation of acute promyelocytic leukemia. Remarkably, blood counts and coagulation parameters were normal. Moreover, no clinical signs of hemorrhage were found. fusion was detected in both laryngeal mass and bone marrow. After diagnosis of APL, ATRA-based chemotherapy was initiated resulting in complete remission of all APL manifestations.

CONCLUSIONS

This is the first case report of APL initially presenting as laryngeal chloroma. Additionally, we performed a comprehensive literature review of previously published extramedullary APL manifestations. In aggregate, a normal blood count at first presentation constitutes an extremely rare finding in patients initially presenting with extramedullary APL manifestations.

摘要

背景

急性早幼粒细胞白血病(APL)是一种严重的血液急症,需要快速诊断和治疗,以预防APL诱导的血小板减少症和凝血病导致的致命性出血。APL的非典型表现,如初次就诊时的髓外疾病,给诊断带来挑战,并延误了适当治疗的开始。然而,APL的髓外表现大多伴有指向潜在血液系统疾病的血细胞计数改变。在本报告中,我们呈现了首例与转移性喉癌极为相似的APL病例,其血细胞计数正常且无凝血病。

病例介绍

一名有吸烟史的67岁男性因进行性声音嘶哑、吞咽痛、吞咽困难和劳力性呼吸困难入院。喉镜检查显示右侧半喉固定,右侧声带活动受限。颈部磁共振成像(MRI)和F-18氟脱氧葡萄糖(FDG)正电子发射断层扫描-计算机断层扫描(PET/CT)显示右侧梨状窝有一个大的高代谢肿瘤,相邻淋巴结有示踪剂摄取,高度怀疑为转移性喉癌。令人惊讶的是,组织学检查显示为急性早幼粒细胞白血病的髓外表现。值得注意的是,血细胞计数和凝血参数正常。此外,未发现出血的临床迹象。在喉部肿块和骨髓中均检测到 融合。诊断为APL后,开始基于全反式维甲酸(ATRA)的化疗,所有APL表现完全缓解。

结论

这是首例最初表现为喉绿色瘤的APL病例报告。此外,我们对先前发表的APL髓外表现进行了全面的文献综述。总体而言,初次就诊时血细胞计数正常在最初表现为APL髓外表现的患者中极为罕见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0235/9174987/a25eccaf7828/fonc-12-886436-g001.jpg

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