Volk Andrea L, Vannucci Stephen A, Cook William, Thompson Keith A, Listinsky Catherine M
Department of Pathology, The University of Alabama at Birmingham, AL 35233-7331, USA.
Ann Diagn Pathol. 2002 Jun;6(3):172-82. doi: 10.1053/adpa.2002.33904.
Concordant or composite mycosis fungoides and B-cell chronic lymphocytic leukemia (B-CLL) is exceedingly rare, with only 10 cases previously described to our knowledge. We report a case of a 64-year-old woman who developed generalized erythroderma 5 years after the diagnosis of early stage B-CLL. Over the next 6 years of her clinical course multiple sequential samples of skin, peripheral blood, and one enlarged lymph node were studied in detail by flow cytometry, immunohistochemistry, molecular diagnostics, and electron microscopy. The progressive cutaneous infiltrates were initially characterized as leukemia cutis, infiltration by B-CLL. Three years later, when she developed worsening skin disease and lymphadenopathy, the cutaneous infiltrates were characterized as cutaneous T-cell lymphoma. At that point, a biopsy of an enlarged lymph node revealed a composite lymphoma of both B-CLL and cutaneous T-cell lymphoma, and the peripheral blood also contained circulating cells of both neoplasms. Herein we summarize the literature on concordant cutaneous T-cell lymphoma and B-CLL, and the literature on concordant T- and B-cell neoplasms in general, with a review of the postulated relationships between these neoplasms.
蕈样肉芽肿与B细胞慢性淋巴细胞白血病(B-CLL)并存或合并的情况极为罕见,据我们所知,此前仅报道过10例。我们报告一例64岁女性,在早期B-CLL诊断5年后出现泛发性红皮病。在其接下来6年的临床病程中,通过流式细胞术、免疫组织化学、分子诊断和电子显微镜对皮肤、外周血的多个连续样本以及一个肿大淋巴结进行了详细研究。进展性皮肤浸润最初被诊断为白血病性皮肤浸润,即B-CLL浸润。三年后,当她的皮肤病和淋巴结病加重时,皮肤浸润被诊断为皮肤T细胞淋巴瘤。此时,对一个肿大淋巴结的活检显示为B-CLL和皮肤T细胞淋巴瘤的复合淋巴瘤,外周血中也含有这两种肿瘤的循环细胞。在此,我们总结了关于蕈样肉芽肿与B-CLL并存的文献,以及关于T细胞和B细胞肿瘤并存的文献,并对这些肿瘤之间的假定关系进行了综述。