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母细胞样浆细胞样树突状细胞瘤中髓系细胞核分化抗原的位点不一致表达。

Site-discordant expression of myeloid cell nuclear differentiation antigen in blastic plasmacytoid dendritic cell neoplasm.

作者信息

Bulterys Philip L, Saleem Atif, Brown Ryanne A, Novoa Roberto A, Rieger Kerri E, Natkunam Yasodha, Fernandez-Pol Sebastian

机构信息

Department of Pathology, Stanford University School of Medicine, Stanford, CA, US.

Department of Dermatology, Stanford University School of Medicine, Stanford, CA, US.

出版信息

Am J Clin Pathol. 2025 Mar 8;163(3):350-356. doi: 10.1093/ajcp/aqae128.

Abstract

OBJECTIVES

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive hematologic neoplasm that can show clinical, morphologic, and immunophenotypic overlap with acute myeloid leukemia. Myeloid cell nuclear differentiation antigen (MNDA) is a nuclear protein expressed by myelomonocytic cells previously reported to be reliably absent in BPDCN and proposed as a useful adjunct for the distinction of BPDCN and acute myeloid leukemia. We encountered a case of BPDCN that showed strong nuclear expression of MNDA in bone marrow and breast samples and weak to absent expression in skin samples, prompting us to reevaluate the expression of MNDA in BPDCN.

METHODS

We collected all available BPDCN cases from the Stanford University archives collected in the past 10 years and subjected them to MNDA immunohistochemistry. In select cases, molecular profiling by next-generation sequencing was performed.

RESULTS

We found 4 cases (of 8 total examined [50%]) with convincing site-discordant MNDA expression. This expression was seen in 3 of 6 (50%) bone marrow samples, 1 of 2 (50%) breast soft tissue samples, and 3 of 14 (up to 21%) skin samples and was not obviously predicted by age, sex, history of myeloid neoplasm, or treatment history. In 2 cases, MNDA was strongly expressed in 2 distinct sites (breast/bone marrow, skin/bone marrow) and negative in subsequent samples.

CONCLUSIONS

Our findings suggest that MNDA expression in BPDCN is anatomic site dependent and transient, with noncutaneous infiltrates showing more frequent expression than cutaneous infiltrates. These results caution against the use of MNDA to exclude BPDCN when considering the differential diagnosis of a blastic extramedullary infiltrate.

摘要

目的

母细胞性浆细胞样树突状细胞肿瘤(BPDCN)是一种罕见且侵袭性强的血液系统肿瘤,在临床、形态学和免疫表型上可能与急性髓系白血病重叠。髓系细胞核分化抗原(MNDA)是一种由髓单核细胞表达的核蛋白,此前报道在BPDCN中可靠缺失,并被提议作为区分BPDCN和急性髓系白血病的有用辅助指标。我们遇到一例BPDCN病例,其骨髓和乳腺样本中MNDA呈强核表达,而皮肤样本中表达较弱或无表达,这促使我们重新评估MNDA在BPDCN中的表达情况。

方法

我们收集了斯坦福大学档案库中过去10年的所有可用BPDCN病例,并对其进行MNDA免疫组化检测。在部分病例中,进行了二代测序的分子谱分析。

结果

我们发现8例受检病例中有4例(占50%)存在令人信服的部位不一致的MNDA表达。这种表达在6例骨髓样本中的3例(占50%)、2例乳腺软组织样本中的1例(占50%)以及14例皮肤样本中的3例(高达21%)中可见,且年龄、性别、髓系肿瘤病史或治疗史均未明显预测到这种表达。在2例病例中,MNDA在2个不同部位(乳腺/骨髓、皮肤/骨髓)呈强表达,而在后续样本中为阴性。

结论

我们的研究结果表明,BPDCN中MNDA的表达取决于解剖部位且具有短暂性,非皮肤浸润比皮肤浸润表现出更频繁的表达。这些结果提醒在考虑母细胞性髓外浸润的鉴别诊断时,谨慎使用MNDA来排除BPDCN。

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