4.3 Article

Recurrent endobronchial occlusion and aorto-bronchial fistula formation in Behcet's disease

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JOURNAL OF CARDIOTHORACIC SURGERY
卷 18, 期 1, 页码 -

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BMC
DOI: 10.1186/s13019-023-02145-0

关键词

Behcet's disease; Mouth and Genital ulcers with inflamed cartilage (MAGIC) syndrome; Endobronchial occlusion; Descending thoracic aortic aneurysm

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This case report presents a 44-year-old woman with Behcet's Disease, Mouth and Genital ulcers with inflamed cartilage (MAGIC) syndrome and an aortic Frozen Elephant Trunk (FET). The patient experienced recurrent left lobar collapse of the lung and was found to have inflammatory endobronchial webs as well as an aorto-bronchial fistula. Despite medical management and surgical intervention, the patient's left bronchial tree continued to occlude, resulting in chronic collapse of the lung.
Background Behcet's disease is a multi-system inflammatory disorder. A small subset of patients with Behcet's develop relapsing polychondritis which is classified as a separate disease known as Mouth and Genital ulcers with inflamed cartilage (MAGIC syndrome). It has previously been observed that this condition can also affect the cartilaginous tissue in the tracheobronchial tree. Case presentation We present the case of a 44-year-old lady with Behcet's Disease, Mouth and Genital ulcers with inflamed cartilage (MAGIC) syndrome and an aortic Frozen Elephant Trunk (FET) who presented to hospital with recurrent episodes of left lobar collapse of the lung. During bronchoscopy, we found the presence of multiple inflammatory endobronchial webs occluding segments of the left bronchial tree. Repeated examinations showed evidence that these inflammatory webs were progressing in size, density and location. Furthermore, we noticed herniation of her descending aortic FET into her left bronchial tree forming an aorto-bronchial fistula which was complicated by a graft infection. Her descending aortic FET section was surgically replaced with an open procedure and bronchoscopic interventions attempted to remove the occlusions in her bronchial tree. Despite optimisation of medical management and surgical correction, this patient continued to develop progressive occlusion of her left bronchial tree, resulting in a chronically collapsed left lung. Conclusions A multi-disciplinary team approach is of paramount importance in order to optimally manage patients with Behcet's disease, balancing immunosuppressive regimens that need close monitoring and titration in the context of potential surgical intervention and the risk for intercurrent infection.

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