血性胸腔积液中细胞学检测出的多形性脂肪肉瘤:通过细胞学线索和细胞阻断免疫细胞化学减少陷阱。

IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Diagnostic Cytopathology Pub Date : 2024-08-27 DOI:10.1002/dc.25399
Badr AbdullGaffar, Tasnim Keloth
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引用次数: 0

摘要

肉瘤性浆液性渗出液并不常见,在诊断上具有挑战性。脱分化和多形性脂肪肉瘤是胸腔积液中罕见的肿瘤,可显示高度多形性的肿瘤细胞,模仿癌、间皮瘤、黑色素瘤和其他肉瘤。血胸腔积液使细胞学诊断更加复杂。正确的细胞学识别非常重要。我们报告了在一名 56 岁男性的渗出液中细胞学检测到多形性脂肪肉瘤的病例,该患者出现大量单侧胸腔积液。ThinPrep 显示出血性渗出液的特征是溶解的红细胞、泡沫状巨噬细胞和嗜酸性粒细胞与高度多形性的裸单核和巨核混杂在一起。聚集的嗜酸性粒细胞和空泡状巨噬细胞可能被误认为是肿瘤细胞,而裸核则可能被误认为是非特异性变性变化。细胞块切片显示高度多形的单核和多核巨型肿瘤细胞,带有诊断性脂母细胞,与泡沫状巨噬细胞和嗜酸性粒细胞混杂在一起。细胞块免疫细胞化学显示,肿瘤细胞中有波形蛋白和S-100蛋白染色。其他细胞系特异性免疫标志物呈阴性。CD68 和钙网蛋白显示,背景巨噬细胞频繁出现,间皮细胞稀少。肿瘤细胞的 MDM2 和 CDK4 阴性。细胞病理学诊断为多形性脂肪肉瘤。对肿块进行了穿刺活检。组织病理学特征和组织标本的免疫图谱与细胞病理学和免疫细胞化学结果相符,证实了多形性脂肪肉瘤的细胞学诊断。多形性脂肪肉瘤是一种意想不到的具有细胞学挑战性的流出液发现,尤其是当血丝液带来的隐患时更是如此。注意某些细胞学线索可减少误诊。细胞阻滞与相关的阴性和阳性免疫细胞化学标记物相结合,是一种有价值的诊断工具。
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Pleomorphic Liposarcoma Cytologically Detected in Hemosiderotic Pleural Effusion: Pitfalls Mitigated by Cytologic Clues and Cellblock Immunocytochemistry.

Sarcomatous serous effusions are uncommon and diagnostically challenging. Dedifferentiated and pleomorphic liposarcomas are rare tumors in pleural effusions revealing highly pleomorphic tumor cells mimicking carcinoma, mesothelioma, melanoma, and other sarcomas. Hematothoracic effusions further complicate the cytologic diagnosis. Correct cytologic recognition is important. We report pleomorphic liposarcoma cytologically detected in effusion fluid in a 56-year-old man who presented with a massive unilateral pleural effusion. ThinPrep showed hemorrhagic effusion fluid characterized by lysed red blood cells, foamy macrophages, and siderophages intermixed with highly pleomorphic predominantly naked mononuclear and giant nuclei. The aggregated siderophages and vacuolated macrophages could be mistaken for tumor cells, whereas the bare nuclei may be missed as nonspecific degenerate changes. Cellblock sections showed highly pleomorphic mononuclear and multinucleated giant tumor cells with diagnostic lipoblasts, intermixed with foamy macrophages and siderophages. Cellblock immunocytochemistry showed staining for vimentin and S-100 protein in the tumor cells. Other lineage-specific immunomarkers were negative. CD68 and calretinin revealed frequent background macrophages and scarce mesothelial cells. The tumor cells were negative for MDM2 and CDK4. The entertained cytopathologic diagnosis was pleomorphic liposarcoma. Core needle biopsy was procured from the mass. The histopathologic features and immunoprofile of the tissue specimen matched the cytopathologic and immunocytochemical findings confirming the cytologic diagnosis of pleomorphic liposarcoma. Pleomorphic liposarcoma is an unexpected cytologically challenging finding in effusions, particularly when compounded by pitfalls introduced by hemosiderotic fluid. Attention to certain cytologic clues mitigate pitfalls. Cellblock is a valuable diagnostic tool when integrated with relevant negative and positive immunocytochemical markers.

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来源期刊
Diagnostic Cytopathology
Diagnostic Cytopathology 医学-病理学
CiteScore
2.60
自引率
7.70%
发文量
163
审稿时长
3-6 weeks
期刊介绍: Diagnostic Cytopathology is intended to provide a forum for the exchange of information in the field of cytopathology, with special emphasis on the practical, clinical aspects of the discipline. The editors invite original scientific articles, as well as special review articles, feature articles, and letters to the editor, from laboratory professionals engaged in the practice of cytopathology. Manuscripts are accepted for publication on the basis of scientific merit, practical significance, and suitability for publication in a journal dedicated to this discipline. Original articles can be considered only with the understanding that they have never been published before and that they have not been submitted for simultaneous review to another publication.
期刊最新文献
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