Seol Jung Eun, Hong Seong Min, Ahn Sang Woo, Kim Jong Uk, Cho Gyeong Je, Jin Woo Jung, Park So Hee, Kim Hyojin
Department of Dermatology, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
Ann Dermatol. 2023 May;35(Suppl 1):S76-S78. doi: 10.5021/ad.21a.028.
After anaplastic large-cell lymphoma (ALCL) was first described by Stain in 1985, there have been several histological variants of ALCL reported. There are classified histological subtypes of ALCL, such as lymphohistiocytic, small cell, Hodgkin-like, composite pattern, and other less common variants including neutrophil-rich ALCL. A 63-year-old male patient presented with erythematous exophytic mass on the left lower leg. In the past, his condition had been diagnosed as abdominal primary cutaneous ALCL (pcALCL), which recurred as systemic ALCL (sALCL) in the left bronchus. After treatment, he achieved complete remission. Histopathologic examination showed large-sized pleomorphic, anaplastic mitotic tumor cells, several neutrophils, and a few lymphocytes. Neutrophil-rich ALCL is a rare histological variant of ALCL. It is characterized by the presence of CD30-positive anaplastic tumor cells with numerous neutrophil infiltrations. Neutrophil-rich ALCL responds well to treatment but tends to recur. There were four cases reported to have recurrent neutrophil-rich ALCL. All cases were diagnosed with neutrophil-rich pcALCL prior to recurrence. Three cases had local recurrence, and only one case relapsed as sALCL. Herein, we present the first case of neutrophil-rich ALCL recurring as sALCL twice.
1985年,斯坦因首次描述间变性大细胞淋巴瘤(ALCL)后,已有多种ALCL的组织学变异型被报道。ALCL有分类的组织学亚型,如淋巴组织细胞型、小细胞型、霍奇金样型、复合模式型,以及其他不太常见的变异型,包括富含中性粒细胞的ALCL。一名63岁男性患者左小腿出现红斑性外生性肿块。过去,他的病情被诊断为腹部原发性皮肤ALCL(pcALCL),后来在左支气管复发为系统性ALCL(sALCL)。经过治疗,他实现了完全缓解。组织病理学检查显示有大的多形性、间变性有丝分裂肿瘤细胞、几个中性粒细胞和一些淋巴细胞。富含中性粒细胞的ALCL是ALCL一种罕见的组织学变异型。其特征是存在CD30阳性的间变性肿瘤细胞并伴有大量中性粒细胞浸润。富含中性粒细胞的ALCL对治疗反应良好,但容易复发。有4例报告患有复发性富含中性粒细胞的ALCL。所有病例在复发前均被诊断为富含中性粒细胞的pcALCL。3例局部复发,只有1例复发为sALCL。在此,我们报告首例富含中性粒细胞的ALCL两次复发为sALCL的病例。