Ito Tsuyoshi, Koyama Satoshi, Iwamoto Shotaro, Hirayama Masahiro, Azuma Eiichi
Department of Pediatrics, Toyohashi Municipal Hospital, Toyohashi, Aichi, Japan.
Department of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.
Am J Case Rep. 2018 Nov 5;19:1317-1323. doi: 10.12659/AJCR.911701.
BACKGROUND Acquired platythorax, or flattening of the chest with a reduction in the anteroposterior (AP) diameter, is very rare and the prognosis depends on the degree of the deformity, respiratory function, and on any underlying disease. Drug-induced pulmonary fibrosis is associated with pulmonary hypoplasia. A case of acquired platythorax is presented in a young man previously treated with cyclophosphamide in childhood. CASE REPORT A 20-year-old man began to experience cough, chest pain, and mild exertional dyspnea. He was admitted to the hospital at 23 years of age with respiratory failure. Chest imaging showed pleural thickening and platythorax. He had been successfully treated for acute lymphoblastic leukemia (ALL), at 3 years of age, with chemotherapy that included a cumulative dose of cyclophosphamide of 15.6 g/m². His ALL relapsed six years later and he was the treated again with cyclophosphamide and underwent a second and complete remission. A clinical diagnosis of late-onset cyclophosphamide-induced lung disease with progressive platythorax was made on the basis of his clinical history and on imaging findings of the ratio of the AP to lateral chest wall diameter when compared with age-matched controls. Despite continued remission of his ALL, he died of progressive cardiopulmonary failure at 25 years of age. CONCLUSIONS This report described a rare case of acquired platythorax, or flattening of the chest, in a young adult. The use of the ratio of the chest wall AP diameter to lateral diameter may be used in the early detection of this rare chemotherapy-induced complication in children and adults.
背景 后天性扁平胸,即胸部变平且前后径减小,非常罕见,其预后取决于畸形程度、呼吸功能以及任何潜在疾病。药物性肺纤维化与肺发育不全有关。本文报告一例曾在儿童期接受环磷酰胺治疗的年轻男性后天性扁平胸病例。病例报告 一名20岁男性开始出现咳嗽、胸痛和轻度劳力性呼吸困难。他23岁时因呼吸衰竭入院。胸部影像学检查显示胸膜增厚和扁平胸。他3岁时曾成功接受急性淋巴细胞白血病(ALL)化疗,环磷酰胺累积剂量为15.6 g/m²。他的ALL在6年后复发,再次接受环磷酰胺治疗并实现第二次完全缓解。根据他的临床病史以及与年龄匹配对照组相比的胸部前后径与侧胸壁直径比值的影像学检查结果,做出了迟发性环磷酰胺诱导的肺部疾病伴进行性扁平胸的临床诊断。尽管他的ALL持续缓解,但他在25岁时死于进行性心肺衰竭。结论 本报告描述了一例年轻成年人后天性扁平胸(即胸部变平)的罕见病例。胸壁前后径与侧径的比值可用于早期发现儿童和成人中这种罕见的化疗引起的并发症。