Nind N R, Attanoos R L, Gibbs A R
Department of Histopathology, Llandough Hospital, Cardiff and Vale NHS Trust, Cardiff, UK.
Histopathology. 2003 Feb;42(2):150-5. doi: 10.1046/j.1365-2559.2003.01555.x.
Malignant pleural mesothelioma is known to mimic morphologically a number of diverse reactive and neoplastic conditions. We describe three unusual intraparenchymal growth patterns of malignant mesothelioma seen in a series of 200 malignant pleural mesotheliomas. The diagnostic pitfalls associated with these findings are described and their potential medico-legal implications are highlighted.
The study group comprised 200 malignant pleural mesotheliomas. In each case diagnosis was morphologically confirmed with ancillary immunohistochemistry using a broad panel of both mesothelial and epithelial markers. The patterns of intraparenchymal growth were documented and grouped as: direct subpleural; lymphangitic; and other. The 200 malignant pleural mesotheliomas comprised 118 epithelioid, 57 biphasic and 25 sarcomatoid, subtyped according to the WHO classification. Direct subpleural invasion was seen in 42 cases, lymphangitic spread in 27 cases. Other less well-defined intraparenchymal patterns included three sarcomatoid subtype malignant mesotheliomas exhibiting an intra-alveolar growth pattern mimicking epithelioid haemangioendothelioma. One epithelioid subtype malignant mesothelioma contained an intraparenchymal tumour nodule microscopically comprising lepidic spread of neoplastic cells over maintained alveolar structures mimicking bronchioloalveolar carcinoma. One epithelioid subtype malignant mesothelioma morphologically had areas in which alveoli were distended by discohesive epithelioid neoplastic cells with no interstitial invasion. The appearances mimicked desquamative interstitial pneumonia. Immunohistochemistry played an important role in the definitive diagnosis of each unusual parenchymal tumour deposit. In 126 malignant mesotheliomas no invasion of the subjacent lung parenchyma was identified.
An awareness of the unusual parenchymal growth pattern in malignant mesothelioma is important to prevent misdiagnosis of other entities. In the medico-legal setting, the presence of epithelioid haemangioendothelioma or bronchioloalveolar carcinoma (in the absence of asbestosis) may be deemed to impact upon the patient's anticipated life expectancy and thereby would decrease the compensation settlement.
已知恶性胸膜间皮瘤在形态上可模仿多种不同的反应性和肿瘤性病变。我们描述了在200例恶性胸膜间皮瘤系列病例中观察到的恶性间皮瘤的三种不寻常的实质内生长模式。描述了与这些发现相关的诊断陷阱,并强调了它们潜在的法医学意义。
研究组包括200例恶性胸膜间皮瘤。每例病例均通过使用一系列间皮和上皮标志物的辅助免疫组织化学在形态学上确诊。记录实质内生长模式并分为:直接胸膜下型;淋巴管型;以及其他类型。这200例恶性胸膜间皮瘤根据世界卫生组织分类法分为118例上皮样型、57例双向型和25例肉瘤样型。42例可见直接胸膜下侵犯,27例可见淋巴管扩散。其他不太明确的实质内模式包括三例肉瘤样型恶性间皮瘤呈现模仿上皮样血管内皮瘤的肺泡内生长模式。一例上皮样型恶性间皮瘤在显微镜下含有一个实质内肿瘤结节,由肿瘤细胞在维持的肺泡结构上的鳞屑样扩散组成,模仿细支气管肺泡癌。一例上皮样型恶性间皮瘤在形态上有肺泡被离散的上皮样肿瘤细胞扩张而无间质侵犯的区域。其表现模仿脱屑性间质性肺炎。免疫组织化学在每个不寻常的实质肿瘤沉积物的明确诊断中起重要作用。在126例恶性间皮瘤中未发现对下方肺实质的侵犯。
认识到恶性间皮瘤中不寻常的实质生长模式对于防止误诊为其他疾病很重要。在法医学环境中,上皮样血管内皮瘤或细支气管肺泡癌(在无石棉沉着病的情况下)的存在可能被认为会影响患者的预期寿命,从而减少赔偿金额。