“…An 17 examples of spontaneous rupture of the branches of LSA in patients including ours (Table 1 ), have been reported in the literature. [ 4 – 18 ] The most common clinical feature of rupture was pain (70.6%, 12/17) with the position of chest, back, and neck, others included sensory deficit (23.5%, 4/17), expanding mass (17.6%, 3/17), dyspnea (17.6%, 3/17), stridor (11.8%, 2/17), hae- mothorax (11.8%, 2/17), and dysphagia (5.9%, 1/17). Among these 17 patients, we found that spontaneous rupture was happened with congenital or acquired vascular anomalies of the aortic arch, comprised of aberrant LSA itself, such as aneurysms (58.8%, 10/17), right aortic arch (RAA) (17.6%, 3/17), aortic dissection (11.8%, 2/17), and aortic coarctation (5.9%, 1/17).10 of 17 patients with von Recklinghausen's disease (VRD) (neurofibromatosis) had rupture of LSA, which was considered as mainly hereditary disease that was at risk of rupturing of LSA.…”