Diagnose: Subcutaneous panniculitis-like t cell lymphoma (SPTCL).
诊断：皮下脂膜炎样T细胞淋巴瘤。
Objective: To investigate the clinical and pathological features of SPTCL.
目的：探讨皮下脂膜炎样t细胞淋巴瘤的临床和病理特征。
Conclusion: SPTCL is not rare in cutaneous non-Hodgkin's lymphoma in children.
结论：SPTCL在儿童皮肤非何杰金淋巴瘤中并不少见。
Results The main clinical manifestations of SPTCL was the single or multiple subcutaneous nodules.
结果SPTCL主要表现为皮下结节，单发或多发。
Objective to analyzes the histopathological and clinical features for diagnosis of subcutaneous panniculitis like t cell lymphoma (SPTCL).
目的：观察皮下脂膜炎样T细胞淋巴瘤(SPTCL)的临床表现并分析SPTCL的病理组织学形态、诊断及鉴别诊断。
Objective To study the clinicopathological features, the immunophenotyping, the gene rearrangement and the prognosis of subcutaneous panniculitis-like T-cell lymphoma (SPTCL).
目的研究皮下脂膜炎样T细胞淋巴瘤的临床病理特征、免疫表型、基因重排和预后。
Objective To study the clinicopathological features, the immunophenotyping, the gene rearrangement and the prognosis of subcutaneous panniculitis-like T-cell lymphoma (SPTCL).
目的研究皮下脂膜炎样T细胞淋巴瘤的临床病理特征、免疫表型、基因重排和预后。
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