Sir: Congenital peribronchial myofibroblastic tumour (CPMT) is a rare neoplasm, with only 15 cases having been reported in the literature. Herein, we report two cases of CPMT in Vietnamese infants: case 1 was a pre-term female at 32.5 weeks of gestation; case 2 was a full-term female. Both presented with leukocytosis, tac-hypnoea, and respiratory distress, with pyrexia and cyanosis in case 2. Computed tomography showed a solid mass (52 x 40 x 40 mm) replacing the left inferior lung in case 1, and a solid mass (65 x 50 x 50 mm) with fine air cysts replacing the right inferior lung in case 2.
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机译：主席先生：先天性支气管周肌成纤维细胞瘤（CPMT）是一种罕见的肿瘤，文献中仅报道了15例。本文中，我们报道了越南婴儿中的两例CPMT：病例1是妊娠32.5周的早产女性;病例1是妊娠32.5周的早产女性。案例2是一名足月女性。病例2均表现为白细胞增多，tac呼吸不足和呼吸窘迫，并伴有发热和发。计算机断层扫描显示，病例1的实心肿块（52 x 40 x 40 mm）代替了左下肺，实心的肿块（65） x 50 x 50 mm），并在第2种情况下用细小的空气囊代替了右下肺。
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