Brodlie M, Barwick S C, Wood K M, McKean M C, Welch A
Department of Respiratory Paediatrics, Newcastle upon Tyne Hospitals NHS Foundation Trust, Freeman Hospital, Newcastle upon Tyne, UK.
J Laryngol Otol. 2011 Aug;125(8):865-8. doi: 10.1017/S0022215111000648. Epub 2011 Apr 12.
To highlight the clinical importance of inflammatory myofibroblastic tumours of the respiratory tract in children, and to present a case series of three children which illustrates this tumour's variable clinical presentation.
The series includes: a nine-year-old girl with a diagnosis of juvenile idiopathic arthritis, who presented with finger clubbing and was found to have an inflammatory myofibroblastic tumour in her right upper lobe; a 15-year-old adolescent with a left main stem bronchial inflammatory myofibroblastic tumour, who presented with breathlessness and chest pain; and a 12-year-old girl with a tracheal inflammatory myofibroblastic tumour who presented with stridor. In each case, the tumour was resected surgically.
Inflammatory myofibroblastic tumour are a rare but clinically important and pathologically distinct lesion of the respiratory tract in children. The cases in this series highlight some of the varied clinical presentations of inflammatory myofibroblastic tumours, and illustrate some of this tumour's different anatomical locations within the paediatric respiratory tract.
强调儿童呼吸道炎性肌纤维母细胞瘤的临床重要性,并呈现一组三个儿童病例,以说明该肿瘤多样的临床表现。
该病例组包括:一名诊断为幼年特发性关节炎的9岁女孩,出现杵状指,被发现右上叶有炎性肌纤维母细胞瘤;一名15岁青少年,患有左主支气管炎性肌纤维母细胞瘤,表现为呼吸急促和胸痛;以及一名12岁女孩,患有气管炎性肌纤维母细胞瘤,表现为喘鸣。在每个病例中,肿瘤均通过手术切除。
炎性肌纤维母细胞瘤是儿童呼吸道一种罕见但临床重要且病理特征明显的病变。该病例组突出了炎性肌纤维母细胞瘤的一些多样临床表现,并说明了该肿瘤在儿童呼吸道内的一些不同解剖位置。