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1.
J Cardiothorac Surg ; 10: 61, 2015 Apr 26.
Article in English | MEDLINE | ID: mdl-25928343

ABSTRACT

OBJECTIVE: Scarf pin inhalation is becoming a frequent accident among young Moroccan woman who wears islamic veil. The aim of the study is to highlight indications, principles and challenges of surgical removal of that particular foreign body. METHODS: Twenty-eight patients were hospitalized in Thoracic Surgery department of Ibn Sina Hospital at Rabat between January 2008 and June 2013 for surgical removal of a pin scarf after unsuccessful endoscopy. RESULTS: Mean age was 20 years. Inhalation was accidental in all cases. Average interval between inhalation and surgery was 10 days. Penetration syndrome was found in 82% of patients. Pin was located at the left tracheo-bronchial tree in 53.5% of cases and at the right one in 46.4%. All were operated by thoracotomy. Surgery was conservative in all cases, and postoperative course was uneventful. CONCLUSION: In case of failure endoscopic treatment, surgery remains the only alternative. It must be as conservative as possible. Short interval between inhalation accident and surgery prevents parenchymal resection.


Subject(s)
Bronchi/surgery , Foreign Bodies/surgery , Respiratory Aspiration/surgery , Trachea/surgery , Wounds, Penetrating , Bronchi/injuries , Bronchoscopy , Cohort Studies , Female , Humans , Morocco , Thoracotomy , Trachea/injuries , Treatment Failure , Young Adult
2.
Eur J Cardiothorac Surg ; 44(6): 1137-9, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23644714

ABSTRACT

We report a rare case of a giant desmoid tumour responsible for cardiac and respiratory failure. Complete removal was decided upon, despite an initial failure in another centre because of symptom severity. In such cases, wide local resection remains the best therapeutic approach, but the risk of local recurrence is high. Literature review confirms the exceptional presentation and the benefit of aggressive surgery.


Subject(s)
Fibromatosis, Aggressive/physiopathology , Heart Failure/etiology , Mediastinal Neoplasms/physiopathology , Female , Fibromatosis, Aggressive/diagnostic imaging , Fibromatosis, Aggressive/pathology , Fibromatosis, Aggressive/surgery , Humans , Mediastinal Neoplasms/diagnostic imaging , Mediastinal Neoplasms/pathology , Mediastinal Neoplasms/surgery , Mediastinum/diagnostic imaging , Mediastinum/pathology , Mediastinum/surgery , Middle Aged , Radiography
8.
Cases J ; 2: 8235, 2009 Sep 03.
Article in English | MEDLINE | ID: mdl-19918408

ABSTRACT

INTRODUCTION: The pulmonary epithelioid hemangioendothelioma is a rare vascular intermediate malignancy tumour. CASE PRESENTATION: A 45-year-old man, he shows an isolated chronic cough with a preserved general state of health. The thoracoabdominal Computed tomography showed three well limited opacities of the right lung, among them one shows some calcifications; which we entirely resected by enucleation after a pneumotomy. The histologic examination with immunomarking led to an epithelioid hemangioendothelioma. CONCLUSIONS: The pulmonary epithelioid hemangioendothelioma is a tumour of unpredictable prognosis, bad when linked to the plurifocal and symptomatic forms.

9.
Cases J ; 2: 6377, 2009 Jul 21.
Article in English | MEDLINE | ID: mdl-19829798

ABSTRACT

Benign neoplasm of the endobronchial tree is quite rare, while endobronchial lipoma is extremely rare. The irreversible pulmonary damage is due to progressive bronchial obstruction; even so, pleural empyema is exceptionally encountered in a case of endobronchial lipoma. We report a case of a 47-year-old man who had left lung pneumonia with hemoptysis. The chest computed tomography showed cystic bronchiectasis with pleural effusion, Flexible bronchoscopy revealed a round tumor on the left main bronchus.

10.
Cases J ; 2: 8555, 2009 Jul 16.
Article in English | MEDLINE | ID: mdl-19830084

ABSTRACT

Leiomyoma of the mediastinum is rare. We report a case of a 57-year-old woman with a cervical mass diving to the intrathoracic. Chest radiography and computed tomography revealed a mass in the right superior mediastinum. The tumor was enucleated by cervicotomy. Histologically, the tumor was diagnosed as leiomyoma.

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