AlKhamisy Ayman, Abbas Walaa, Barakat Aya, Ghabreau Lina, Khanji Khaled, Morjan Mohamad
Pediatric Surgery Section, Aleppo University Hospital, Aleppo, Syria.
Pediatric Surgery Section, Aleppo University Hospital, Aleppo, Syria.
Int J Surg Case Rep. 2023 Jul;108:108461. doi: 10.1016/j.ijscr.2023.108461. Epub 2023 Jul 4.
Pleuropulmonary blastoma is a rare, aggressive intrathoracic neoplasm of early childhood.
We report a case of a 4-month-old male baby who has presented with recurrent respiratory infections since birth. A surgical team was consulted due to abnormal opacification observed on a chest X-ray. An enhanced-contrast CT scan of the chest revealed a heterogenous, well-delineated mass measuring about 3,8 × 6 cm in the posterior mediastinum. A left posterolateral thoracotomy was performed. The mass was separated from the lung parenchyma, located behind the parietal pleura, and adherent to the chest wall and superior ribs. The lesion was totally removed. Histologically, the lesion was a pleuropulmonary blastoma type III. Currently, the patient is on a 6-month course of chemotherapy.
The aggressive, insidious behavior of PPB requires a high index of suspicion for diagnosis. The clinical manifestations and imaging modalities are atypical and nonspecific. However, PPB should be kept in mind when a huge solid or cystic mass is observed in the lung field on imaging.
Extrapulmonary pleuropulmonary blastoma is a very rare entity characterized by highly aggressive behavior and a poor prognosis. Early excision of thoracic cystic lesions in children is warranted regardless of the symptoms to avoid future mishaps.
胸膜肺母细胞瘤是一种罕见的、侵袭性的儿童期胸内肿瘤。
我们报告一例4个月大男婴,自出生以来反复出现呼吸道感染。因胸部X线检查发现异常致密影而咨询外科团队。胸部增强CT扫描显示后纵隔有一个大小约3.8×6cm的不均匀、边界清晰的肿块。行左后外侧开胸手术。肿块与肺实质分离,位于脏层胸膜后方,与胸壁和上位肋骨粘连。病变被完全切除。组织学检查显示,该病变为III型胸膜肺母细胞瘤。目前,患者正在接受为期6个月的化疗。
胸膜肺母细胞瘤的侵袭性、隐匿性行为需要高度怀疑以进行诊断。其临床表现和影像学表现不典型且无特异性。然而,当影像学检查在肺野中观察到巨大实性或囊性肿块时,应考虑胸膜肺母细胞瘤。
肺外型胸膜肺母细胞瘤是一种非常罕见的疾病,具有高度侵袭性和不良预后。无论有无症状,均有必要早期切除儿童胸内囊性病变,以避免未来发生意外。