Simon S R, Dorighi J A, Branda R F, Ershler W B
Med Pediatr Oncol. 1985;13(6):390-1. doi: 10.1002/mpo.2950130618.
Horner's Syndrome (ptosis, anisocoria, and anhydrosis) developed in a 22-year-old woman. A mediastinal mass was noted on chest x-ray. Further evaluation led to a diagnosis of Hodgkin's disease, nodular sclerosis type. Horner's syndrome is an unusual initial manifestation of Hodgkin's disease, and, in this case, it was due to oculosympathetic damage from mediastinal compression. Because the potential for cure is high in Hodgkin's disease, this diagnosis should be considered in patients presenting with Horner's syndrome.
一名22岁女性出现了霍纳综合征（上睑下垂、瞳孔不等大及无汗）。胸部X线检查发现纵隔肿物。进一步评估后诊断为结节硬化型霍奇金淋巴瘤。霍纳综合征是霍奇金淋巴瘤不常见的首发表现，在本例中，其病因是纵隔压迫导致的眼交感神经损伤。由于霍奇金淋巴瘤的治愈率较高，对于出现霍纳综合征的患者应考虑这一诊断。
