Jan Iftikhar Ahmad, AlKaabi Saif Khalfan, AlMughadam Awadh, Murthy D Sreenivas, AlHamoudi Basmah
Department of Pediatric Surgery, Zayed Military Hospital, Abu Dhabi, United Arab Emirates.
Department of Pediatric Medicine, Zayed Military Hospital, Abu Dhabi, United Arab Emirates.
Afr J Paediatr Surg. 2016 Oct-Dec;13(4):202-205. doi: 10.4103/0189-6725.194676.
Glanzmann's thrombasthenia (GT) is a rare autosomal recessive disorder in which the platelets have anomalies of fibrinogen receptors causing bleeding tendencies. The disease usually presents with mucosal bleeding, petechial haemorrhages or gastrointestinal (GI) bleeding. Only sporadic cases of intussusception or duodenal haematoma have been reported with GT. We present a case of 5-year-old girl admitted with non-bilious vomiting, watery diarrhoea and abdominal pain. She is a known patient of Glanzmann's thrombasthenia.
血小板无力症(GT)是一种罕见的常染色体隐性疾病,该病患者的血小板存在纤维蛋白原受体异常,从而导致出血倾向。该病通常表现为黏膜出血、瘀点出血或胃肠道出血。仅有关于血小板无力症并发肠套叠或十二指肠血肿的散发病例报道。我们报告了一例5岁女童,因非胆汁性呕吐、水样腹泻和腹痛入院。她是一名已知的血小板无力症患者。