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软骨黏液样纤维瘤的细胞病理学:2 例 GRM1 免疫细胞化学表达的报告。

Cytopathology of Chondromyxoid Fibroma: Report of 2 Cases with Immunocytochemical Expression of GRM1.

机构信息

Department of Pathology, Teikyo University School of Medicine, Tokyo, Japan.

Department of Pathology, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan.

出版信息

Acta Cytol. 2024;68(1):66-72. doi: 10.1159/000536459. Epub 2024 Jan 27.

Abstract

INTRODUCTION

Chondromyxoid fibroma (CMF) is a rare, benign bone tumor that occurs predominantly in the second and third decades of life, more frequently in males. Overexpression of GRM1 as a consequence of tumor-specific gene rearrangement of GRM1 has recently been reported as a useful immunohistochemical marker for histopathological diagnosis of CMF. However, the usefulness of GRM1 staining of cytology specimens has not yet been evaluated. In this report, the cytological findings and GRM1 immunocytochemistry of two cases of CMF are described.

CASE PRESENTATIONS

Case 1 was a 15-year-old girl with a rib tumor. Imaging findings suggested a benign neurogenic tumor such as schwannoma. The tumor had increased in size over a 2-year period and was resected. Case 2 was a 14-year-old boy with a metatarsal tumor involving his left first toe. Imaging findings were suspicious of a benign neoplastic lesion. Biopsy findings suggested a benign tumor, and the patient underwent tumor resection. Cytologically, in both cases the tumor cells were predominantly spindle-shaped or stellate, with a myxoid to chondromyxoid background matrix and multinucleated giant cells, and these matrices were metachromatic with Giemsa staining. Cellular atypia was more accentuated in case 2 than in case 1. Immunocytochemical staining for GRM1 was positive in both cases.

CONCLUSION

Due to the overlap in cytological findings, it is often difficult to differentiate CMF from chondroblastoma and chondrosarcoma grade 2. Immunocytochemical staining for GRM1 may support the diagnosis of CMF, and the reuse of Papanicolaou-stained specimens is applicable. The present cases further demonstrated the difficulty of differentiating CMF from other mimicking tumors such as chondroblastoma and chondrosarcoma grade 2. In such instances, immunocytochemistry for GRM1 is applicable to the diagnostic process, the value of which is strengthened by reusing Papanicolaou-stained specimens.

摘要

简介

软骨黏液样纤维瘤(CMF)是一种罕见的良性骨肿瘤,主要发生在第二和第三个十年,男性多见。最近有报道称,GRM1 的肿瘤特异性基因重排导致其过度表达,可作为 CMF 组织病理学诊断的一种有用的免疫组织化学标志物。然而,GRM1 染色细胞学标本的有用性尚未得到评估。本报告描述了 2 例 CMF 的细胞学表现和 GRM1 免疫细胞化学染色。

病例介绍

病例 1 为 15 岁女孩,肋骨肿瘤。影像学表现提示为良性神经源性肿瘤,如神经鞘瘤。肿瘤在 2 年内逐渐增大,予以切除。病例 2 为 14 岁男孩,左足第一跖骨肿瘤。影像学表现提示为良性肿瘤病变。活检结果提示为良性肿瘤,患者行肿瘤切除术。细胞学上,在这两种情况下,肿瘤细胞主要呈纺锤形或星状,黏液样到软骨样基质和多核巨细胞,这些基质用吉姆萨染色呈异染性。2 号病例的细胞异型性比 1 号病例更明显。GRM1 的免疫细胞化学染色均为阳性。

结论

由于细胞学表现有重叠,CMF 与软骨母细胞瘤和 2 级软骨肉瘤通常难以区分。GRM1 的免疫细胞化学染色可能有助于 CMF 的诊断,且可重复使用巴氏染色标本。本病例进一步表明,CMF 与其他类似肿瘤,如软骨母细胞瘤和 2 级软骨肉瘤的鉴别具有一定难度。在这种情况下,GRM1 的免疫细胞化学染色可应用于诊断过程,通过重复使用巴氏染色标本,其价值得到增强。

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