S. Mansoor, K. Murphy, M. Adenan, E. Joyce, O. Hardiman, Michael J. Hennessey, S. Kelly
{"title":"平山病:一种罕见的临床疾病","authors":"S. Mansoor, K. Murphy, M. Adenan, E. Joyce, O. Hardiman, Michael J. Hennessey, S. Kelly","doi":"10.5455/sajem.020204","DOIUrl":null,"url":null,"abstract":"Hirayama disease is a rare neurological entity which can present in any setting emergency departments included. These cases are usually diagnosed after carefully excluding other conditions. Intraspinal lesions (eg, syringomyelia, syringobulbia, or tumor) can present with symptoms that can mimic hirayama disease. We report the case of a 23-year old man who presented with an 18 month history of numbness, tingling and painless curling of the 4th and 5th digits. The symptoms did not progress beyond the 12 month period. The right side and bulbar function remained unaffected throughout. Based on the age of onset, arrest of progression after a period of deterioration, imaging features and neurophysiological findings a diagnosis of Hirayama Disease was made.","PeriodicalId":389251,"journal":{"name":"South Asian Journal of Emergency Medicine","volume":"64 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hirayama Disease: A Rare Clinical Entity\",\"authors\":\"S. Mansoor, K. Murphy, M. Adenan, E. Joyce, O. Hardiman, Michael J. Hennessey, S. Kelly\",\"doi\":\"10.5455/sajem.020204\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hirayama disease is a rare neurological entity which can present in any setting emergency departments included. These cases are usually diagnosed after carefully excluding other conditions. Intraspinal lesions (eg, syringomyelia, syringobulbia, or tumor) can present with symptoms that can mimic hirayama disease. We report the case of a 23-year old man who presented with an 18 month history of numbness, tingling and painless curling of the 4th and 5th digits. The symptoms did not progress beyond the 12 month period. The right side and bulbar function remained unaffected throughout. Based on the age of onset, arrest of progression after a period of deterioration, imaging features and neurophysiological findings a diagnosis of Hirayama Disease was made.\",\"PeriodicalId\":389251,\"journal\":{\"name\":\"South Asian Journal of Emergency Medicine\",\"volume\":\"64 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"South Asian Journal of Emergency Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5455/sajem.020204\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"South Asian Journal of Emergency Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5455/sajem.020204","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Hirayama disease is a rare neurological entity which can present in any setting emergency departments included. These cases are usually diagnosed after carefully excluding other conditions. Intraspinal lesions (eg, syringomyelia, syringobulbia, or tumor) can present with symptoms that can mimic hirayama disease. We report the case of a 23-year old man who presented with an 18 month history of numbness, tingling and painless curling of the 4th and 5th digits. The symptoms did not progress beyond the 12 month period. The right side and bulbar function remained unaffected throughout. Based on the age of onset, arrest of progression after a period of deterioration, imaging features and neurophysiological findings a diagnosis of Hirayama Disease was made.