Xu Jie, Hsi Eric D, Miranda Roberto N, Marques-Piubelli Mario L, Medeiros L Jeffrey, Feldman Andrew L
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States.
Am J Clin Pathol. 2025 Jul 11;164(1):110-125. doi: 10.1093/ajcp/aqaf029.
Anaplastic large cell lymphoma (ALCL) cases were discussed at the 2023 Society of Hematopathology/European Association for Haematopathology workshop held on November 9-11, 2023, in Houston, Texas. This session focused on the clinical and pathologic spectrum of 3 types of ALCL: anaplastic lymphoma kinase (ALK)-positive, ALK-negative, and breast implant associated (BIA). Cases of primary cutaneous ALCL were excluded because they were included in another session. Although the diagnosis of ALCL is often straightforward, the 42 submitted cases encompassed unusual clinical presentations, morphologic variants, and atypical immunophenotypes, exemplifying potential difficulties and challenges in establishing the diagnosis of ALCL. Distinguishing ALCL from CD30-positive peripheral T-cell lymphoma, not otherwise specified, or classic Hodgkin lymphoma was discussed. In patients with a previous history of mycosis fungoides and other T-cell lymphoma/leukemia, the differential diagnosis of a CD30-positive T-cell lymphoma mimicking ALCL (mycosis fungoides transformation vs de novo ALCL) was also discussed. In patients with suspected BIA-ALCL, it is critical to properly handle the periprosthetic fluid when the disease first presents and the capsule at the time of initial capsulectomy to make a correct diagnosis and pathologic staging because a missed diagnosis may lead to disease progression. Comprehensive immunohistochemical analysis; fluorescence in situ hybridization for DUSP22, TP63, or JAK2 rearrangement; assessment of clonality of the T-cell receptor and immunoglobulin genes; and sequencing for mutations were performed as part of the workup of the submitted cases, particularly on ALK-negative ALCL cases, emphasizing the importance of ancillary testing in establishing the diagnosis.
2023年11月9日至11日在得克萨斯州休斯敦举行的2023年血液病理学学会/欧洲血液病理学协会研讨会上讨论了间变性大细胞淋巴瘤(ALCL)病例。本次会议聚焦于3种类型ALCL的临床和病理谱:间变性淋巴瘤激酶(ALK)阳性、ALK阴性和乳腺植入物相关(BIA)。原发性皮肤ALCL病例被排除,因为它们被纳入了另一场会议。尽管ALCL的诊断通常很直接,但提交的42例病例涵盖了不寻常的临床表现、形态学变异和非典型免疫表型,例证了在确立ALCL诊断时可能遇到的困难和挑战。讨论了将ALCL与未另行指定的CD30阳性外周T细胞淋巴瘤或经典霍奇金淋巴瘤相鉴别。对于有蕈样肉芽肿和其他T细胞淋巴瘤/白血病既往史的患者,也讨论了模仿ALCL的CD30阳性T细胞淋巴瘤的鉴别诊断(蕈样肉芽肿转化与原发性ALCL)。对于疑似BIA-ALCL的患者,在疾病首次出现时正确处理假体周围液体以及在初次包膜切除时处理包膜对于做出正确诊断和病理分期至关重要,因为漏诊可能导致疾病进展。作为提交病例检查工作的一部分,进行了全面的免疫组化分析;针对DUSP22、TP63或JAK2重排的荧光原位杂交;T细胞受体和免疫球蛋白基因克隆性评估;以及突变测序,特别是在ALK阴性ALCL病例中,强调了辅助检测在确立诊断中的重要性。