Department of Cytology and Gynecologic Pathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Department of Pathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Diagn Cytopathol. 2024 Feb;52(2):103-115. doi: 10.1002/dc.25254. Epub 2023 Nov 14.
Pleuropulmonary blastoma (PPB) is a rare, aggressive, primary intrathoracic malignancy typically seen in infancy and early childhood. Accurate distinction from congenital cystic lung lesions is crucial due to significant prognostic and therapeutic differences. Cytologic features have rarely been described. Establishing a cytodiagnosis is challenging owing to its rarity, lack of awareness, and multiple morphologic mimics.
This was a retrospective study conducted over 8 years. The histopathology and cytopathology databases were searched for all pediatric PPB cases. The corresponding cytologic samples were reviewed to identify characteristic features that can help distinguish PPB from its mimics.
There was a total of six cases of pediatric PPB reported during the study period. Of these, four (66.7%) presented as intrathoracic, and two (33.3%) as pleural-based masses. Cytology smears showed discretely scattered and perivascular arrangements of round-oval tumor cells with background eosinophilic stromal material. The tumor cells were mildly pleomorphic (n = 3) with round nuclei, fine chromatin, inconspicuous nucleoli, and scanty cytoplasm; however, three cases showed marked anaplasia, and one each showed necrosis and rhabdoid differentiation. On immunocytochemistry (4/6), these were positive for vimentin and desmin and negative for WT1, chromogranin, SALL4, cytokeratin, CD45, and CD99. FISH (1/6) did not show N-Myc amplification.
Knowledge of the characteristic cytomorphological and immunocytochemical features of PPB is vital to establish a prompt and accurate cytodiagnosis with appropriate clinicoradiologic correlation.
胸膜肺母细胞瘤(PPB)是一种罕见的、侵袭性的原发性胸腔恶性肿瘤,通常见于婴儿和幼儿期。由于预后和治疗方法存在显著差异,准确地区分与先天性囊性肺病变至关重要。细胞学特征很少被描述。由于其罕见性、缺乏认识以及多种形态模拟物的存在,建立细胞学诊断具有挑战性。
这是一项为期 8 年的回顾性研究。在组织病理学和细胞病理学数据库中搜索了所有小儿 PPB 病例。回顾了相应的细胞学样本,以确定有助于将 PPB 与其模拟物区分开来的特征。
在研究期间共报告了 6 例小儿 PPB。其中,4 例(66.7%)表现为胸腔内,2 例(33.3%)为胸膜基肿块。细胞学涂片显示圆形-椭圆形肿瘤细胞呈离散散在排列和围绕血管排列,背景为嗜酸性基质物质。肿瘤细胞轻度多形性(n=3),圆形核,细染色质,不明显核仁,细胞质稀少;然而,有 3 例表现出明显的间变,1 例各表现出坏死和横纹肌样分化。免疫细胞化学(4/6)显示波形蛋白和结蛋白阳性,WT1、嗜铬粒蛋白、SALL4、细胞角蛋白、CD45 和 CD99 阴性。荧光原位杂交(1/6)未显示 N-Myc 扩增。
了解 PPB 的特征性细胞形态学和免疫细胞化学特征对于建立及时准确的细胞学诊断并结合适当的临床放射学相关性至关重要。