Rare benign lung tumours presenting with high clinical suspicion for malignancy: a case series and review of the literature.

IF 1.7 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Folia histochemica et cytobiologica Pub Date : 2023-01-01 DOI:10.5603/FHC.a2023.0011
Katarina Popovic, Mirjana Miladinović, Ljiljana Vučković, Mirjana Nedović Vuković
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Abstract

Introduction: Incidentally discovered lung nodules can be worrisome for both the patient and their physicians. Although 95% of solitary lung nodules are benign, it is important to distinguish which nodules have high clinical suspicion for malignancy. Existing clinical guidelines do not apply to patients with signs and symptoms related to the lesion and with an increased baseline risk of lung cancer or metastasis. This paper highlights the vital role of pathohistological analysis and immunohistochemistry in the definitive diagnosis of such incidentally discovered lung nodules.

Material and methods: The three cases presented were selected based on their similar clinical presentations. A review of the literature was performed using the online database PubMed, for articles published in the period between January of 1973 to February of 2023 using the following medical subject headlines: "primary alveolar adenoma," "alveolar adenoma," "primary pulmonary meningioma," "pulmonary meningioma," and "pulmonary benign metastasizing leiomyoma." Results (Case Series). The case series consists of three incidentally discovered lung nodule(s). Although they presented with high clinical suspicion for malignancy, detailed workup confirmed the diagnosis of three rare benign lung tumours: primary alveolar adenoma, primary pulmonary meningioma, and benign metastasizing leiomyoma.

Conclusions: Clinical suspicion for malignancy in the presented cases arose from previous and current medical history of malignancy, family history of malignancy, and/or specific radiographic findings. This paper highlights the need for a multidisciplinary approach in the management of incidentally discovered pulmonary nodules. Excisional biopsy and pathohistological analysis remain the gold standard in confirming the presence of a pathologic process and determining the nature of the disease. Common features of the diagnostic algorithm utilized among the three cases include multi-slice computerized tomography, excisional biopsy via atypical wedge resection (if the nodule is peripherally located), and lastly, pathomorphological analysis using haematoxylin and eosin staining and immunohistochemistry.

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临床高度怀疑为恶性的罕见良性肺肿瘤:病例系列及文献回顾。
偶然发现的肺结节对患者和医生来说都是令人担忧的。虽然95%的孤立性肺结节是良性的,但鉴别哪些结节临床怀疑为恶性是很重要的。现有临床指南不适用于与病变相关的体征和症状以及肺癌或转移基线风险增加的患者。本文强调病理组织学分析和免疫组织化学在明确诊断这种偶然发现的肺结节中的重要作用。材料与方法:选取临床表现相近的3例病例。使用PubMed在线数据库对1973年1月至2023年2月期间发表的文章进行文献回顾,使用以下医学主题标题:“原发性肺泡腺瘤”、“肺泡腺瘤”、“原发性肺脑膜瘤”、“肺脑膜瘤”和“肺良性转移性平滑肌瘤”。结果(病例系列)。该病例系列包括三个偶然发现的肺结节。虽然临床表现为高度的恶性怀疑,但详细的检查证实了三种罕见的良性肺肿瘤的诊断:原发性肺泡腺瘤、原发性肺脑膜瘤和良性转移性平滑肌瘤。结论:这些病例的临床怀疑为恶性肿瘤,是由于既往和当前的恶性病史、恶性家族史和/或特定的影像学表现。本文强调需要一个多学科的方法在管理偶然发现的肺结节。切除活检和病理组织分析仍然是确认病理过程存在和确定疾病性质的金标准。三个病例的诊断算法的共同特征包括多层计算机断层扫描,非典型楔形切除活检(如果结节位于周围),最后使用血红素和伊红染色和免疫组织化学进行病理形态学分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Folia histochemica et cytobiologica
Folia histochemica et cytobiologica 生物-生化与分子生物学
CiteScore
2.80
自引率
6.70%
发文量
56
审稿时长
6-12 weeks
期刊介绍: "Folia Histochemica et Cytobiologica" is an international, English-language journal publishing articles in the areas of histochemistry, cytochemistry and cell & tissue biology. "Folia Histochemica et Cytobiologica" was established in 1963 under the title: ‘Folia Histochemica et Cytochemica’ by the Polish Histochemical and Cytochemical Society as a journal devoted to the rapidly developing fields of histochemistry and cytochemistry. In 1984, the profile of the journal was broadened to accommodate papers dealing with cell and tissue biology, and the title was accordingly changed to "Folia Histochemica et Cytobiologica". "Folia Histochemica et Cytobiologica" is published quarterly, one volume a year, by the Polish Histochemical and Cytochemical Society.
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