Al-Trabolsi Hassan A, Alshehri Mohammed, Al-Shomrani Ali, Shabanah Medhat, Al-Barki Ahmed A
Department of Pediatrics, Hematology/Oncology, Aseer Central Hospital, College of Medicine, King Khalid University, Abha, Saudi Arabia.
J Pediatr Hematol Oncol. 2006 Feb;28(2):79-81. doi: 10.1097/01.mph.0000199600.57881.b3.
Langerhans cell histiocytosis (LCH) can involve multiple organs. "Primary" or isolated pulmonary LCH is a well-described entity in young adults but is exceedingly rare in children younger than 15 years of age. The authors report a new case in a 2-year-old girl and review other reported cases in the pediatric population. The patient had had respiratory symptoms since early infancy suggestive of hyperactive airway disease. At 2 years of age, she had severe pulmonary insufficiency with remarkable cystic changes noted on chest imaging studies. Biopsy of a pulmonary lesion confirmed the diagnosis of LCH. She had no other organ involvement. Pulmonary histiocytosis, though rare, should be considered in any child with chronic respiratory disease such as bronchial asthma, especially when the response to anti-asthma treatment is poor and/or there are cystic changes on the chest x-ray.
朗格汉斯细胞组织细胞增多症(LCH)可累及多个器官。“原发性”或孤立性肺LCH在年轻成人中是一种已被充分描述的病症,但在15岁以下儿童中极为罕见。作者报告了一名2岁女孩的新病例,并回顾了儿科人群中其他已报告的病例。该患者自婴儿早期就有呼吸道症状,提示患有气道高反应性疾病。2岁时,她出现严重的肺功能不全,胸部影像学检查发现明显的囊性改变。肺部病变活检确诊为LCH。她没有其他器官受累。对于任何患有慢性呼吸道疾病(如支气管哮喘)的儿童,尤其是对抗哮喘治疗反应不佳和/或胸部X线有囊性改变的儿童,即使肺组织细胞增多症罕见,也应予以考虑。