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一名17岁男孩的恶性胸膜间皮瘤:病例报告及文献综述

Malignant pleural mesothelioma in a 17-year old boy: A case report and literature review.

作者信息

Pérez-Guzmán C, Barrera-Rodríguez R, Portilla-Segura J

机构信息

Hospital General Tercer Milenio. Instituto de Salud del Estado de Aguascalientes, Av. Siglo XXI s/n Col. Satélite Morelos, Aguascalientes 20140, México.

Depto. de Bioquímica y Medicina Ambiental, Instituto Nacional de Enfermedades Respiratorias-SSA, Clza. Tlalpan, 4502, Col Sec. XVI. México, D.F., 14080, México.

出版信息

Respir Med Case Rep. 2016 Jan 20;17:57-60. doi: 10.1016/j.rmcr.2016.01.005. eCollection 2016.

DOI:10.1016/j.rmcr.2016.01.005
PMID:27222787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4821324/
Abstract

BACKGROUND

Malignant pleural mesothelioma is a rare, invasive and often fatal neoplasm that develops in the thin layer of tissue surrounding the lungs known as the pleura. Although rare, mesotheliomas do occur in the young; their characteristics are distinct from those of older patients.

CASE PRESENTATION

This is a case report of a 17-year-old boy who had moderate dyspnea, cough, right-sided pleuritic chest pain, fever, headache and no weight loss. Physical examination showed a right pleural effusion and chest roentgenograms revealed a homogenous opacity on lower right hemithorax. Biochemical analysis of pleural fluid showed hemorrhagic/turbid effusion compatible with exudate. It was initially treated as an empyema. The pleural fluid culture was negative. Adenosine deaminase level was 34.3 U/L (admission) and 19.02 U/L (two weeks after). Pleural fluid smear and culture for Mtb were negative. During the open pleural biopsy, thickened pleura and multiple pale yellow nodules in the lung were observed. The histopathological report was compatible with malignant pleural mesothelioma. With this diagnosis, a chemotherapy regimen with cisplatin was initiated. After two cycles, the patient had no clinical and radiological improvement. The patient is currently under regular follow up.

CONCLUSION

MPM is rare in young adults and its clinical presentation makes it different from mesothelioma in elderly patients, so it will be necessary to identify the new risk factors that can identify these patients.

摘要

背景

恶性胸膜间皮瘤是一种罕见、侵袭性且往往致命的肿瘤,发生于围绕肺部的薄层组织即胸膜中。尽管罕见,但间皮瘤确实会在年轻人中出现;其特征与老年患者不同。

病例报告

本文报告一名17岁男孩,有中度呼吸困难、咳嗽、右侧胸膜炎性胸痛、发热、头痛,无体重减轻。体格检查显示右侧胸腔积液,胸部X线片显示右下胸部有均匀的不透光区。胸腔积液生化分析显示为血性/浑浊积液,符合渗出液。最初按脓胸治疗。胸腔积液培养为阴性。腺苷脱氨酶水平入院时为34.3 U/L,两周后为19.02 U/L。结核分枝杆菌胸腔积液涂片及培养均为阴性。在开放性胸膜活检时,观察到胸膜增厚及肺内多个淡黄色结节。组织病理学报告符合恶性胸膜间皮瘤。基于此诊断,开始使用顺铂的化疗方案。两个周期后,患者在临床和影像学上均无改善。患者目前正在接受定期随访。

结论

恶性胸膜间皮瘤在年轻人中罕见,其临床表现与老年患者的间皮瘤不同,因此有必要确定可识别这些患者的新危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65bf/4821324/df11b0c8b023/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65bf/4821324/2da400f309d0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65bf/4821324/df11b0c8b023/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65bf/4821324/2da400f309d0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65bf/4821324/df11b0c8b023/gr2.jpg

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Rare Tumors in Children: Progress Through Collaboration.儿童罕见肿瘤:通过合作取得进展。
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Distinctive clinical characteristics of malignant mesothelioma in young patients.年轻患者恶性间皮瘤的独特临床特征。
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Gene-asbestos interaction in malignant pleural mesothelioma susceptibility.恶性胸膜间皮瘤易感性中的基因-石棉相互作用。
Carcinogenesis. 2015 Oct;36(10):1129-35. doi: 10.1093/carcin/bgv097. Epub 2015 Jul 2.
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Mesothelioma patients with germline BAP1 mutations have 7-fold improved long-term survival.胚系 BAP1 突变的间皮瘤患者的长期生存率提高了 7 倍。
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Germline mutation of Bap1 accelerates development of asbestos-induced malignant mesothelioma.Bap1的种系突变加速石棉诱导的恶性间皮瘤的发展。
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BAP1 and cancer.BAP1 与癌症。
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All-cause mortality and cancer incidence among adults exposed to blue asbestos during childhood.儿童时期接触青石棉的成年人的全因死亡率和癌症发病率。
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Malignant pleural mesothelioma presenting with a spontaneous hydropneumothorax: a report of 2 cases.以自发性血气胸为表现的恶性胸膜间皮瘤:2例报告
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