Pleuropulmonary Blastoma (PPB) in Child with DICER1 Mutation: The First Case Report in the State of Qatar.

Q4 Medicine Case Reports in Pulmonology Pub Date : 2021-10-29 eCollection Date: 2021-01-01 DOI:10.1155/2021/1983864
Sara G Hamad, Amal Al-Naimi, Mutasim Abu-Hasan
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引用次数: 2

Abstract

Pleuropulmonary blastoma (PPB) is a rare intrathoracic malignancy, which arises from the lung parenchyma and/or pleura. PPB has strong genetic association with mutations in DICER1 gene. Despite being rare, PPB is the most common lung tumor in children below 6 years of age. International registry of the disease has a total of 350 cases worldwide. We report the first case of PPB in the state of Qatar, which presented as a large cystic lung lesion. The patient was first thought to have benign congenital pulmonary airway malformation (CPAM) based on chest X-ray findings. The diagnosis of PPB was suspected based on chest CT scan findings and was confirmed after surgical resection of the cystic mass. The case highlights the need to consider PPB in the differential diagnosis of cystic lung lesions in children and the need for further radiological imaging (i.e., CT scan), genetic testing, and/or excisional biopsy to confirm the diagnosis.

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DICER1突变儿童胸膜肺母细胞瘤(PPB):卡塔尔第一例报告。
胸膜肺母细胞瘤(PPB)是一种罕见的胸内恶性肿瘤,起源于肺实质和/或胸膜。PPB与DICER1基因突变有较强的遗传相关性。尽管罕见,但PPB是6岁以下儿童中最常见的肺部肿瘤。该疾病的国际登记在全世界共有350个病例。我们报告的第一例PPB在卡塔尔的状态,这是一个大的囊性肺病变。患者首先被认为是良性先天性肺气道畸形(CPAM)基于胸部x线检查结果。PPB的诊断是基于胸部CT扫描结果,并在手术切除囊性肿块后得到证实。该病例强调了在鉴别诊断儿童囊性肺病变时需要考虑PPB,并需要进一步的放射成像(即CT扫描)、基因检测和/或切除活检来确认诊断。
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来源期刊
Case Reports in Pulmonology
Case Reports in Pulmonology Medicine-Pulmonary and Respiratory Medicine
CiteScore
1.80
自引率
0.00%
发文量
23
审稿时长
13 weeks
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