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浅表性 CD34 阳性纤维母细胞肿瘤的临床病理和分子研究,这些肿瘤类似于非典型纤维组织细胞瘤(纤维瘤病)。

Clinicopathologic and molecular study of superficial CD34-positive fibroblastic tumours mimicking atypical fibrous histiocytoma (dermatofibroma).

机构信息

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.

出版信息

Histopathology. 2024 Dec;85(6):939-949. doi: 10.1111/his.15282. Epub 2024 Jul 24.

DOI:10.1111/his.15282
PMID:39044682
Abstract

AIMS

Superficial CD34-positive fibroblastic tumour (SCD34FT) is an uncommon but distinctive low-grade neoplasm of the skin and subcutis that shows frequent CADM3 expression by immunohistochemistry (IHC). In this study, prompted by an index case resembling 'atypical fibrous histiocytoma (FH)' that was positive for CADM3 IHC, we systematically examined a cohort of tumours previously diagnosed as 'atypical FH' by applying CADM3 and fluorescence in situ hybridization (FISH) for PRDM10 rearrangement, to investigate the overlap between these tumour types.

METHODS AND RESULTS

Forty cases of atypical FH were retrieved, including CD34-positive tumours (n = 20) and CD34-negative tumours (n = 20). All tumours were stained for CADM3. All CADM3-positive tumours were evaluated by FISH to assess for PRDM10 rearrangement. Eleven CD34-positive tumours (11/20, 55%) coexpressed CADM3 and were reclassified as SCD34FT. None (0/20) of the CD34-negative atypical FH were CADM3-positive. Reclassified SCD34FT (10/11) arose on the lower extremity, with frequent involvement of the thigh (n = 8). Features suggestive of atypical FH were observed in many reclassified cases including variable cellularity, spindled morphology, infiltrative tumour margins, collagen entrapment, epidermal hyperpigmentation, and acanthosis. Variably prominent multinucleate giant cells, including Touton-like forms, were also present. An informative FISH result was obtained in 10/11 reclassified tumours, with 60% (6/10) demonstrating PRDM10 rearrangement.

CONCLUSION

A significant subset of tumours that histologically resemble atypical FH, and are positive for CD34, coexpress CADM3 and harbour PRDM10 rearrangement, supporting their reclassification as SCD34FT. Awareness of this morphologic overlap and the application of CADM3 IHC can aid the distinction between SCD34FT and atypical FH.

摘要

目的

表皮 CD34 阳性纤维母细胞瘤(SCD34FT)是一种罕见但具有特征性的皮肤和皮下组织的低级肿瘤,免疫组织化学(IHC)常显示 CADM3 表达。在本研究中,受一个类似于“非典型纤维组织细胞瘤(FH)”的索引病例的启发,该病例 CADM3 IHC 阳性,我们系统地检查了一组先前通过 CADM3 和荧光原位杂交(FISH)检测 PRDM10 重排诊断为“非典型 FH”的肿瘤,以研究这些肿瘤类型之间的重叠。

方法和结果

共检索到 40 例非典型 FH 病例,包括 CD34 阳性肿瘤(n=20)和 CD34 阴性肿瘤(n=20)。所有肿瘤均进行 CADM3 染色。所有 CADM3 阳性肿瘤均通过 FISH 评估 PRDM10 重排。11 例 CD34 阳性肿瘤(11/20,55%)共表达 CADM3,并重新分类为 SCD34FT。无 CD34 阴性非典型 FH(0/20)为 CADM3 阳性。重新分类的 SCD34FT(10/11)发生在下肢,大腿受累频繁(n=8)。许多重新分类的病例观察到提示非典型 FH 的特征,包括细胞多样性、梭形形态、浸润性肿瘤边界、胶原捕获、表皮色素沉着和棘皮症。也存在不同程度突出的多核巨细胞,包括 Touton 样形式。10/11 例重新分类的肿瘤获得了有意义的 FISH 结果,60%(6/10)显示 PRDM10 重排。

结论

一组组织学上类似于非典型 FH 的肿瘤,且 CD34 阳性,共表达 CADM3 并具有 PRDM10 重排,支持将其重新分类为 SCD34FT。认识到这种形态学重叠,并应用 CADM3 IHC,可以帮助区分 SCD34FT 和非典型 FH。

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