首页> 外文期刊>Iranian journal of pediatrics >Congenital Insensitivity to Pain with Anhidrosis (HSAN Type IV), Extremely Rare Syndrome that Can Be Easily Missed by Bone and Joint Surgeons: A Case Report
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Congenital Insensitivity to Pain with Anhidrosis (HSAN Type IV), Extremely Rare Syndrome that Can Be Easily Missed by Bone and Joint Surgeons: A Case Report

机译:先天性对无汗症疼痛(HSAN IV型),骨骼和关节外科医生容易错过的罕见罕见综合症的不敏感性:一例报告

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BackgroundCongenital insensitivity to pain with anhidrosis is an extremely rare disorder in which injuries can often be missed by patient, parents and even by orthopedic surgeon. Pain and tenderness, on which a trauma team so much depends to make a clinical diagnosis and to decide whether to go for radiological evaluation can be misleading in this rare syndrome. So complete clinical examination still forms the corner stone to avoid misdiagnosis and pick up the rare disorders.Case PresentationWe present a 5 year old girl child, who was brought to us as a case of one and a half month old neglected trauma left leg and was diagnosed to be suffering from congenital insensitivity to pain with anhidrosis (HSAN Type IV).ConclusionCongenital insensitivity to pain with anhidrosis is extremely rare entity, in which patients are subjected to repeated injuries which are often neglected. There is no specific treatment but patient training and parent education are key to avoid further neglect and damage.
机译:背景先天性对先天性脱水症的疼痛不敏感是一种极为罕见的疾病,患者,父母甚至整形外科医生常常会错过这种伤害。在这种罕见的综合征中,创伤团队非常依赖疼痛和压痛进行临床诊断并决定是否进行放射学评估可能会产生误导。因此,完整的临床检查仍是避免误诊和发现罕见疾病的基石。病例介绍我们介绍了一个5岁女童,她是一个半月大的被忽视的左腿创伤而被带到我们的。被诊断患有先天性对多汗症的疼痛不敏感(HSAN IV型)。结论先天性对多汗症的疼痛不敏感是极为罕见的实体,在这种情况下,患者经常受到重复伤害而被忽视。没有特殊的治疗方法,但是患者培训和父母教育是避免进一步忽视和损害的关键。

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