Department of Oncology, Huanggang Center Hospital, Huangzhou District, Huanggang.
Department of Pathology.
Medicine (Baltimore). 2021 May 7;100(18):e25770. doi: 10.1097/MD.0000000000025770.
CD30+ primary cutaneous anaplastic large cell lymphoma (PC-ALCL) is a rare T-cell neoplasm, and has been reported to present with an indolent behavior. The PC-ALCL with aggressive behavior has not been reported in the literature.
We treated a patient with PC-ALCL that exhibited indolent behavior in the past 2 years and aggressive behavior within the last 3 months before presentation.
Aggressive CD30+ primary cutaneous anaplastic large cell lymphoma.
The radiotherapy regimen was individualized in terms of the target volume delineation and dose prescription, and the dose-response relationship was evaluated.
The mean distance of microscopic infiltration was 14.1 mm in depth and 14.3 mm circumferentially. The lesion completely regressed after the delivery of 40 Gy in 20 fractions over 4 weeks. The tumor did not recur over the next year.
An aggressive disease course is rare for indolent CD30+ PC-ALCL, which has similar histopathological characteristics as indolent PC-ALCL. The radiotherapy strategy should be individualized with curative intent.
CD30+原发性皮肤间变性大细胞淋巴瘤(PC-ALCL)是一种罕见的 T 细胞肿瘤,其表现为惰性行为已有报道。具有侵袭性行为的 PC-ALCL 在文献中尚未报道。
我们治疗了一名患者,其在过去 2 年内表现为惰性行为,但在就诊前的 3 个月内表现为侵袭性行为。
侵袭性 CD30+原发性皮肤间变性大细胞淋巴瘤。
根据靶区勾画和剂量处方对放疗方案进行个体化,评估剂量反应关系。
显微镜下浸润的平均深度为 14.1mm,周长为 14.3mm。在 4 周内给予 40Gy/20 次分割后,病变完全消退。在接下来的一年中,肿瘤没有复发。
惰性 CD30+PC-ALCL 侵袭性病程罕见,其具有与惰性 PC-ALCL 相似的组织病理学特征。放疗策略应具有治愈意图,进行个体化。