{"title":"50岁患者的先天性囊肿","authors":"Gayatri Harshe, Krishna Mundada","doi":"10.1055/s-0043-1775813","DOIUrl":null,"url":null,"abstract":"In this letter to the editor, we would like to report a case of incidental connatal cyst in a 50-year-old male patient. The patient was on migraine medications; however, he had recurrent episodes of headaches with nausea and was asked to perform a magnetic resonance imaging (MRI) by a treating physician.Thereisnopasthistoryofseizures,paresisorplegia, sensorineural de fi cits, cranial nerve involvement, urinary incontinence, etc. in the patient. The patient was born of a normal delivery at term, with no history of neonatal hospitalization, prolonged jaundice, and respiratory distress. Neurological examination was normal. On MRI, T2-weighted (T2W) coronal images showed bilateral hyperintense cysts located superolaterally to frontal horns ( ► Fig. 1A and B ). Similarly axialT2Wimagesshowedthehyperintensecystanteriortothe frontal horns ( ► Fig. 1C ). On fl uid-attenuated inversion recovery coronal images and T1W, they appeared hypointense ( ► Fig. 2A and B ) without any evidence of associated in fl am-mation and periventricular gliosis. Given the location and no signi fi cantneonatalhistoryinthepatients,the fi ndingsonMRI are consistent with frontal horn cyst aka coarctation of lateral ventricles or connatal cysts. Connatal","PeriodicalId":51597,"journal":{"name":"Indian Journal of Radiology and Imaging","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2023-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Connatal Cyst in a 50-Year-Old Patient\",\"authors\":\"Gayatri Harshe, Krishna Mundada\",\"doi\":\"10.1055/s-0043-1775813\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this letter to the editor, we would like to report a case of incidental connatal cyst in a 50-year-old male patient. The patient was on migraine medications; however, he had recurrent episodes of headaches with nausea and was asked to perform a magnetic resonance imaging (MRI) by a treating physician.Thereisnopasthistoryofseizures,paresisorplegia, sensorineural de fi cits, cranial nerve involvement, urinary incontinence, etc. in the patient. The patient was born of a normal delivery at term, with no history of neonatal hospitalization, prolonged jaundice, and respiratory distress. Neurological examination was normal. On MRI, T2-weighted (T2W) coronal images showed bilateral hyperintense cysts located superolaterally to frontal horns ( ► Fig. 1A and B ). Similarly axialT2Wimagesshowedthehyperintensecystanteriortothe frontal horns ( ► Fig. 1C ). On fl uid-attenuated inversion recovery coronal images and T1W, they appeared hypointense ( ► Fig. 2A and B ) without any evidence of associated in fl am-mation and periventricular gliosis. Given the location and no signi fi cantneonatalhistoryinthepatients,the fi ndingsonMRI are consistent with frontal horn cyst aka coarctation of lateral ventricles or connatal cysts. Connatal\",\"PeriodicalId\":51597,\"journal\":{\"name\":\"Indian Journal of Radiology and Imaging\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2023-10-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Radiology and Imaging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1055/s-0043-1775813\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Radiology and Imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/s-0043-1775813","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
In this letter to the editor, we would like to report a case of incidental connatal cyst in a 50-year-old male patient. The patient was on migraine medications; however, he had recurrent episodes of headaches with nausea and was asked to perform a magnetic resonance imaging (MRI) by a treating physician.Thereisnopasthistoryofseizures,paresisorplegia, sensorineural de fi cits, cranial nerve involvement, urinary incontinence, etc. in the patient. The patient was born of a normal delivery at term, with no history of neonatal hospitalization, prolonged jaundice, and respiratory distress. Neurological examination was normal. On MRI, T2-weighted (T2W) coronal images showed bilateral hyperintense cysts located superolaterally to frontal horns ( ► Fig. 1A and B ). Similarly axialT2Wimagesshowedthehyperintensecystanteriortothe frontal horns ( ► Fig. 1C ). On fl uid-attenuated inversion recovery coronal images and T1W, they appeared hypointense ( ► Fig. 2A and B ) without any evidence of associated in fl am-mation and periventricular gliosis. Given the location and no signi fi cantneonatalhistoryinthepatients,the fi ndingsonMRI are consistent with frontal horn cyst aka coarctation of lateral ventricles or connatal cysts. Connatal