Wollina Uwe, Schmidt Nadine, Schönlebe Jacqueline, Vojvodic Aleksandra, Hansel Gesina, Koch André, Lotti Torello
Department of Dermatology and Allergology, Städtisches Klinikum Dresden, Academic Teaching Hospital, Dresden, Germany.
Institute of Pathology "Georg Schmorl", Städtisches Klinikum Dresden, Academic Teaching Hospital.
Open Access Maced J Med Sci. 2019 Jun 30;7(18):3006-3008. doi: 10.3889/oamjms.2019.565. eCollection 2019 Sep 30.
Cutaneous B-cell lymphomas represent about 25% of all cutaneous lymphomas. Peripheral diffuse large B-cell lymphoma of the leg type is the most aggressive subtype seen mainly in elderly patients. Treatment is not standardised.
An 87-year-old female patient was presented in May 2018 because of the development of painless subcutaneous nodules on the legs since late 2017. On examination, we observed up to 5 cm large erythematous nodules on the legs and a smaller plaque in the left submammary fold. The histology of a skin demonstrated tumour infiltrate that was separated from the overlying epidermis by a grenz zone. It consisted of densely packed, blastoid lymphocytic cells with numerous, and some atypical mitoses. The cells were positive for CD20, CD79A and CD5. Almost 100% of the cells were labelled with Ki67. The diagnosis of a diffuse large B-cell lymphoma (PCLBCL-LT) of the leg was confirmed. Histologic analysis of a bone marrow biopsy demonstrated a hypercellular bone marrow without malignant lymphatic infiltrates. Diagnostic ultrasound of cervical nodes and computerised tomography (CT) scans (native and with contrast medium) of head, neck and trunk excluded an extracutaneous manifestation of the PCLBCL-LT. Treatment with rituximab plus bendamustibe was initiated, but tumour progress was noted after the second course. Suggested palliative therapy with radiation and rituximab was refused. The patient died 7 months after diagnosis.
Although some trials suggested a beneficial effect of immuno-chemotherapy, the prognosis of (PCLBCL-LT) remains poor. Standardised treatment is missing due to the relative rarity of this malignancy.
皮肤B细胞淋巴瘤约占所有皮肤淋巴瘤的25%。腿部外周弥漫性大B细胞淋巴瘤是最具侵袭性的亚型,主要见于老年患者。治疗方法尚未标准化。
一名87岁女性患者于2018年5月就诊,自2017年末起腿部出现无痛性皮下结节。检查时,我们在其腿部观察到直径达5厘米的红斑结节,左乳房下皱襞处有一个较小的斑块。皮肤组织学检查显示肿瘤浸润,其与上方表皮之间有一个无细胞带。肿瘤由密集排列的母细胞样淋巴细胞组成,有许多及一些非典型有丝分裂。这些细胞CD20、CD79A和CD5呈阳性。几乎100%的细胞Ki67标记阳性。确诊为腿部弥漫性大B细胞淋巴瘤(PCLBCL-LT)。骨髓活检的组织学分析显示骨髓细胞增多,无恶性淋巴浸润。颈部淋巴结超声诊断以及头部、颈部和躯干的计算机断层扫描(CT)(平扫和增强)排除了PCLBCL-LT的皮肤外表现。开始使用利妥昔单抗加苯达莫司汀治疗,但在第二个疗程后出现肿瘤进展。建议的放疗和利妥昔单抗姑息治疗被拒绝。患者在诊断后7个月死亡。
尽管一些试验表明免疫化疗有有益效果,但(PCLBCL-LT)的预后仍然很差。由于这种恶性肿瘤相对罕见,缺乏标准化治疗。