Literature DB >> 21645835

[Clinical characteristics of resected bronchial hamartoma. Study of seven cases].

A Zehani-Kassar1, A Ayadi-Kaddour, A Marghli, I Ridene, T Kilani, F El Mezni.   

Abstract

INTRODUCTION: Endobronchial hamartoma is a benign tumour derived from peribronchial mesenchymal tissue. It is a form of intrapulmonary hamartoma and can cause irreversible pulmonary destruction due to bronchial obstruction. Early diagnosis and treatment is very important and endoscopic treatment is usually the first choice. In cases in which prolonged bronchial obstruction has produced irreversible lung destruction surgical, resection of the tumour is necessary. The aim of this study is to describe the clinicopathological characteristics of resected endobronchial hamartoma. PATIENTS AND METHODS: Seven cases of endobronchial hamartoma, diagnosed in our institution between January 1995 and December 2009, were reviewed retrospectively.
RESULTS: The patient population consisted of four males and three females with mean age of 53.7 years (41-68 years). The most frequent clinical presentation was obstructive pneumonia. Endoscopy and imaging showed an endobronchial mass in most cases. Surgical treatment consisted of atypical resection in one case, lobectomy in five cases and pneumonectomy in one case. Tumour size ranged between 0.5 and 3.5 cm. The diagnosis was confirmed in all cases by histological examination. The outcome was favorable in all cases.
CONCLUSION: Endoscopic techniques are effective for the diagnosis and treatment of endobronchial hamartochondroma. Treatment should be prompt to prevent irreversible lung damage due to chronic obstruction and suppuration, in which case, pulmonary resection may be necessary.
Copyright © 2011 SPLF. Published by Elsevier Masson SAS. All rights reserved.

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Year:  2011        PMID: 21645835     DOI: 10.1016/j.rmr.2010.12.006

Source DB:  PubMed          Journal:  Rev Mal Respir        ISSN: 0761-8425            Impact factor:   0.622


  7 in total

1.  [Spontaneous pneumothorax: unusual manifestation of pulmonary hamartochondroma].

Authors:  Hind Serhane; Oussama Abdessalam Afandi; Yassine Msougar; Lamyae Amro
Journal:  Pan Afr Med J       Date:  2016-07-29

2.  An unusual bronchial obstruction in a fit young man.

Authors:  Anna Freeman; David Weeden; Jane Wilkinson; Ramesh J Kurukulaaratchy
Journal:  BMJ Case Rep       Date:  2013-01-09

3.  Two-stage S7 sleeve resection of the right lower lobe and S1+2 and S3 segmentectomy of the left upper lobe: a case report.

Authors:  Waresijiang Yibulayin; Abulimiti Abulaiti; Zhenhua Wu; Xiaohong Sun; Dan He; Keming Xu; Anpeng Ran; Xiayimaierdan Yibulayin; Wei Sun
Journal:  Ann Transl Med       Date:  2021-04

4.  Endobronchial Hamartoma Subtotally Occluding the Right Main Bronchus and Mimicking Bronchial Carcinoid Tumor.

Authors:  Filippo Lococo; Carla Galeone; Luciano Lasagni; Cristiano Carbonelli; Elena Tagliavini; Roberto Piro; Luigi Zucchi; Giorgio Sgarbi
Journal:  Medicine (Baltimore)       Date:  2016-04       Impact factor: 1.889

5.  Endobronchial hamartoma; a rare structural cause of chronic cough.

Authors:  Saman Ahmed; Ayesha Arshad; M Jeffery Mador
Journal:  Respir Med Case Rep       Date:  2017-08-24

6.  Dermatofibrosarcoma protuberans associated with a hamartochondroma of the lung: Diagnostic discussion of a pulmonary nodule.

Authors:  Hicham Harmouchi; Lakranbi Marouane; Rabiou Sani; Issoufou Ibrahim; Ouadnouni Yassine; Smahi Mohammed
Journal:  SAGE Open Med Case Rep       Date:  2019-10-07

Review 7.  Primary Pulmonary Paraganglioma: A Case Report and Review of Literature.

Authors:  Xin Huang; Qi-Lian Liang; Liang Jiang; Qiu-Long Liu; Wen-Ting Ou; Da-Heng Li; Hui-Jie Zhang; Gao-Le Yuan
Journal:  Medicine (Baltimore)       Date:  2015-08       Impact factor: 1.889

  7 in total

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