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伴有CT晕征的肺移植后淋巴组织增生性疾病

Pulmonary post-transplant lymphoproliferative disorder with a CT halo sign.

作者信息

Mucha Krzysztof, Foroncewicz Bartosz, Palczewski Piotr, Sułkowska Katarzyna, Ziarkiewicz-Wróblewska Bogna, Orłowski Tadeusz, Gołębiowski Marek, Pączek Leszek

机构信息

Department of Immunology, Transplantology, and Internal Medicine, Medical University of Warsaw, Warsaw, Poland.

出版信息

Ann Transplant. 2013 Sep 16;18:482-7. doi: 10.12659/AOT.889354.

Abstract

BACKGROUND

Post-transplant lymphoproliferative disease (PTLD) comprises a spectrum of clinically relevant lymphatic diseases that occur in patients after transplantation. The PTLD-related mortality is high and the clinical picture and location of the lesions are very variable. For these reasons, the diagnosis of PTLD is difficult and new diagnostic tools are sought.

CASE REPORT

A 31-year-old woman, 17 years after kidney transplantation, presented with recurrent upper respiratory tract infections, fever, and weakness and was diagnosed with pulmonary PTLD. Computed tomography appearance was not typical for lymphoma and demonstrated multiple bilateral pulmonary nodules and masses with a halo sign. Initial differential diagnosis included invasive pulmonary aspergillosis and acute Wegener granulomatosis. Since cultures from bronchoalveolar lavage and anti-neutrophil cytoplasmic antibodies were negative, videothoracoscopy with lung biopsy was performed. Pathology analysis revealed diffuse large T-cell lymphoma with histopathologic features of infiltrative growth along the lung interstitium, vessel invasion, and hemorrhagic necrosis possibly explaining the presence of a halo sign.

CONCLUSIONS

We suggest PTLD should always be suspected in a transplant recipient presenting with the CT halo sign. Moreover, the correlation of this radiological phenomenon with the patient's clinical presentation and severe pathologic findings allows us to conclude that the thoracic halo sign in PTLD may reflect a worse prognosis.

摘要

背景

移植后淋巴组织增生性疾病(PTLD)包括一系列发生于移植患者的具有临床相关性的淋巴系统疾病。PTLD相关的死亡率很高,且病变的临床表现和部位差异很大。由于这些原因,PTLD的诊断较为困难,因此需要寻找新的诊断工具。

病例报告

一名31岁女性,肾移植17年后,出现反复上呼吸道感染、发热和乏力,被诊断为肺部PTLD。计算机断层扫描表现并非典型的淋巴瘤表现,显示双侧肺部有多个结节和肿块,并伴有晕征。初步鉴别诊断包括侵袭性肺曲霉病和急性韦格纳肉芽肿。由于支气管肺泡灌洗培养和抗中性粒细胞胞浆抗体均为阴性,遂进行了电视胸腔镜检查及肺活检。病理分析显示为弥漫性大T细胞淋巴瘤,其组织病理学特征为沿肺间质浸润性生长、血管侵犯和出血性坏死,这可能解释了晕征的出现。

结论

我们建议,对于出现CT晕征的移植受者应始终怀疑有PTLD。此外,这种放射学现象与患者临床表现及严重病理结果之间的相关性使我们得出结论,PTLD中的胸部晕征可能预示着更差的预后。

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