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Spontaneous Hemothorax in a Patient with von Recklinghausen’s Disease: A Case Report and Review of the Literature
Patient: Male, 45 Final Diagnosis: Spontaneous hemorhorax Symptoms: Cough • worned dyspnea • yellow expectoration Medication: — Clinical Procedure: Chest tube application Specialty: Surgery OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Von Recklinghausen’s disease, also known as T...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543949/ https://www.ncbi.nlm.nih.gov/pubmed/31076564 http://dx.doi.org/10.12659/AJCR.915810 |
Sumario: | Patient: Male, 45 Final Diagnosis: Spontaneous hemorhorax Symptoms: Cough • worned dyspnea • yellow expectoration Medication: — Clinical Procedure: Chest tube application Specialty: Surgery OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Von Recklinghausen’s disease, also known as Type 1 neurofibromatosis (NF1), is a genetic disorder characterized by skin tumors, neurofibromas of multiple organs and vascular abnormalities. Spontaneous thoracic hemorrhage is a rare but potentially fatal consequence of this disorder. After a review of the literature over the last 10 years and on the basis of a case study, the aim of this study was to report the challenges of management of this pathology. CASE REPORT: We report a rare case of a 45-years-old male with a medical history of neurofibromatosis who complained of a 3-day history of progressive dyspnea. At his admission to the Emergency Department, the patient was hemodynamically stable. A chest computed tomography (CT) scan showed a large left hemothorax with mediastinal shift to the right without active bleeding. A chest tube was introduced, and conservative treatment was followed. Another CT scan performed 2 days later revealed a middle lobar pulmonary embolism on the opposite side. A full treatment of anticoagulation was administered, and the patient was released after 8 days of hospitalization. Three weeks later, a new chest CT scan indicated the absence of vascular aneurysm or source for hemothorax. CONCLUSIONS: Our systematic literature review found 15 articles which were described as early as 2005. To our knowledge, endovascular treatment produces the best immediate successful result (100%) and may be used in adjunction with video-assisted thorax surgery (VATS) or thoracic drainage to optimize outcomes. In the present case, conservative treatment showed a good result despite anticoagulation for pulmonary embolism. The endovascular approach seems to be the most promising, but treatment needs to be tailored to each individual patient. |
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