Navigating the diagnostic maze: the challenge of sclerosing pneumocytoma in frozen sections.

IF 1.1 Q4 ONCOLOGY
International journal of clinical and experimental pathology Pub Date : 2024-06-15 eCollection Date: 2024-01-01 DOI:10.62347/KLWT4935
Dina Zenezan, Jiejing Yin, Nikolina Dioufa, Kassaye Firde, Mehri Mollaee, Israh Akhtar
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Abstract

Pulmonary Sclerosing Pneumocytoma (PSP) represents a rare benign tumor that exhibits a predisposition towards females. Often asymptomatic, its identification usually occurs incidentally through imaging modalities. Histologically, PSP demonstrates features consistent with pneumocytic differentiation and possesses a dual-cell population. However, in rare instances it may demonstrate pleural invasion or lymph node metastasis. Diagnosing PSP through small biopsy or frozen section presents considerable challenges attributed to its heterogeneous growth patterns and striking similarity to well-differentiated pulmonary adenocarcinoma. We report a case of PSP in a 57-year-old female smoker, presenting as a slow-growing 2.5 cm mass that recently exhibited enlargement, as noted on computed tomography (CT) scan. The recommendation for excising the mass prompted the patient to undergo a right robotic-assisted thoracoscopic procedure, which entailed wedge resection of the right lower lobe and an intraoperative consultation. A completion right lower lobectomy was performed, accompanied by lymph node dissection, following a frozen section diagnosis indicating at least adenocarcinoma in situ. The permanent section revealed bland cuboidal cells lining papillary and sclerotic areas, with occasional atypical features such as prominent nucleoli and scattered mitotic figures. Adjacent foci of atypical adenomatous hyperplasia (AAH) were noted. Immunohistochemical (IHC) staining revealed positive Napsin A, keratin AE1/3, and CK7 in surface cells but not in round cells. Both EMA and TTF1 immunostains highlighted surface cells and scattered round cells. Elastic stain highlighted visceral pleural involvement. The combined morphology and immunoprofile supported the diagnosis of PSP. This case underscores the critical importance of accurately diagnosing slow-growing pulmonary nodules, which are increasingly detected by the widespread use of imaging for various medical conditions.

探索诊断迷宫:冷冻切片中硬化性肺细胞瘤的挑战。
肺硬化性肺细胞瘤(PSP)是一种罕见的良性肿瘤,好发于女性。这种肿瘤通常没有症状,通常是通过影像学检查偶然发现的。组织学上,PSP 表现出与气细胞分化一致的特征,并具有双细胞群。然而,在极少数情况下,它可能会出现胸膜侵犯或淋巴结转移。通过小切片或冰冻切片诊断 PSP 具有相当大的挑战性,因为它的生长模式不一,而且与分化良好的肺腺癌极为相似。我们报告了一例 PSP 病例,患者是一名 57 岁的女性吸烟者,表现为缓慢生长的 2.5 厘米肿块,最近在计算机断层扫描(CT)中发现肿块增大。切除肿块的建议促使患者接受了右侧机器人辅助胸腔镜手术,包括右下叶楔形切除术和术中会诊。在冰冻切片诊断显示至少为原位腺癌后,进行了完整的右下叶切除术,同时进行了淋巴结清扫。永久切片显示,乳头状和硬化区内有平滑的立方体细胞,偶见不典型特征,如突出的核小体和散在的有丝分裂像。邻近有不典型腺瘤增生(AAH)病灶。免疫组化(IHC)染色显示,表面细胞中的Napsin A、角蛋白AE1/3和CK7呈阳性,但圆形细胞中没有。EMA和TTF1免疫染色均显示表面细胞和散在的圆形细胞。弹性染色突出显示内脏胸膜受累。综合形态学和免疫图谱,支持 PSP 的诊断。该病例强调了准确诊断缓慢生长的肺结节的重要性,随着各种医学影像技术的广泛应用,越来越多的肺结节被发现。
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来源期刊
自引率
0.00%
发文量
42
审稿时长
1 months
期刊介绍: The International Journal of Clinical and Experimental Pathology (IJCEP, ISSN 1936-2625) is a peer reviewed, open access online journal. It was founded in 2008 by an international group of academic pathologists and scientists who are devoted to the scientific exploration of human disease and the rapid dissemination of original data. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal.
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