Imaizumi M, Ichinohasama R, Sato A, Mikami H, Abukawa D, Asanuma A, Aikawa J I, Tanida M, Nakagawa H, Iinuma K
Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Leuk Lymphoma. 1998 Sep;31(1-2):225-9. doi: 10.3109/10428199809057602.
We report a clinicopathologic feature of primary cutaneous T-cell lymphoma (CTCL) in a five-year-old boy with increasing swelling of his cheek since two years of age. Histologically, an infiltrate of atypical lymphoid cells with mature T-cell phenotype and clonality was prominent from the dermis to the subcutaneous tissue of the cheek. Although little effect was seen with aggressive multidrug-combined chemotherapy, therapy with interferon-alpha and steroids achieved a prolonged remission. This patient may provide important clues to understanding the clinicopathologic feature of rare primary CTCL in young children.
我们报告了一名5岁男孩原发性皮肤T细胞淋巴瘤(CTCL)的临床病理特征,自两岁起其脸颊肿胀不断加重。组织学上,从脸颊的真皮层到皮下组织,具有成熟T细胞表型和克隆性的非典型淋巴细胞浸润显著。尽管积极的多药联合化疗效果甚微,但α干扰素和类固醇治疗实现了长期缓解。该患者可能为理解幼儿罕见原发性CTCL的临床病理特征提供重要线索。