alexa Pulmonary Lymphangitic Mesotheliomatosis
ISSN: 2161-105X

Journal of Pulmonary & Respiratory Medicine
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Case Report

Pulmonary Lymphangitic Mesotheliomatosis

Pierre Edde*, Nehme Romy, and Chababi Mirna

Centre Hospitalier Universitaire -Notre Dame De Secours (CHU-NDS) Hospital, Jbeil, Medical school of University Saint Esprit–Kaslik (USEK), Kaslik, Lebanon

*Corresponding Author:
Pierre Edde
Notre Dame De Secours (CHU-NDS) Hospital, Jbeil
Medical school of University Saint Esprit–Kaslik (USEK)
Kaslik, Lebanon
E-mail: [email protected]

Received date: February 04, 2013; Accepted date: February 27, 2013; Published date: March 04, 2013

Citation: Edde P, Romy N, Mirna C (2013) Pulmonary Lymphangitic Mesotheliomatosis. J Pulmon Resp Med 3:136 doi:10.4172/2161-105X.1000136

Copyright: © 2013 Edde P, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.



We report a 45 year old male with right sided pleural mesothelioma who received neoadjuvant chemotherapy prior to a right extrapleural pneumonectomy followed by adjuvant chemotherapy. The patient became tumor free and remained in remission for 19 months following which he developed a lymphangitic spread over the contralateral lung. His diagnosis was confirmed by a bronchoscopic transbronchial biopsy of the left lung. The patient died from progressive respiratory failure over a period of three months. Such a relapse with an aggressive and fatal lymphangitic spread is rarely seen and reported in malignant pleural mesothelioma. Discussion and review of the literature are provided. Mesothelioma is still considered, worldwide, a rare cancer of the serosal membranes. It typically involves the pleural cavity but other reported sites include the peritoneum, pericardium and Tunica vaginalis of the testis. The usual progression of the mesothelioma is coalescence of multiple, small nodules into large masses that invade, entrap and destroy the affected organ by direct extension and invasion. We report an unusual case of relapsing mesothelioma, recurring in an aggressive and fatal form, after 19 months of remission.

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