Itina R I
Vestn Otorinolaringol. 1994 Jan-Feb(1):36-9.
The author considers a rare disease of the sphenopalatine ganglion known in the literature as Sluder's syndrome. In view of the ganglion anatomical structure and connections with afferent and vegetative formations of the face and skull, clinical presentation of the syndrome various greatly. The author analyses the causes of the disease, its differential diagnosis, methods of treatment, gives a case report of a male patient who has been followed up for 26 years to illustrate the complicacy of Sluder's syndrome diagnosis.
作者探讨了一种文献中称为斯卢德综合征的蝶腭神经节罕见疾病。鉴于该神经节的解剖结构以及与面部和颅骨传入及自主神经结构的联系，该综合征的临床表现差异很大。作者分析了该病的病因、鉴别诊断、治疗方法，并给出了一名男性患者的病例报告，该患者已随访26年，以说明斯卢德综合征诊断的复杂性。
