Vinogradova Iu E, Giliazitdinova E A, Zamulaeva I A, Zybunova E E, Kaplanskaia I B, Kravchenko S K, Kremenetskaia A M, Lutsenko I N, Samoĭlova R S, Selivanova E N, Sidorova Iu V, Shklovskiĭ-Kord N E
Ter Arkh. 2005;77(10):61-5.
To try a combined approach to the study of clinicomorphological and immunophenotypical characteristics of primary cutaneous T-cell lymphomas.
Clinical, histological, genotypic and immunophenotypical parameters were studied in 7 patients (4 male and 3 female, mean age 53.1 +/- 7.8%) with Sezary's disease (SD) and 10 patients (6 male, 4 female, mean age 54.0 +/- 4.0 years) with mycosis fungoides (MF) treated in Hematological Research Center in 1998-2004.
Six of seven SD patients had SD stage IV with leukemization, Sezary's cells were found in peripheral blood. Bone marrow and lymph nodes involvement was observed in 5 patients. Morphological signs of transformation into lymphosarcoma were detected in three patients. Skin samples of all the patients showed epidermotropism with lymphoid infiltration of the derma and skin appendages. All the patients had clonal rearrangement of T-cell receptor by gamma-chain. Immunophenotyping (IPT) detected T-cell markers CD45RO, CD43, CD3, CD4 on lymphoid cells. IPT of peripheral blood lymphoid cells was typical for SD in 3 patients. Low density of CD4 and CD2, CD4 and CD5, the presence of CD7 were registered in 1 patient each. The disease history was 3.4 +/- 0.7 years. A lethal outcome was related with septic complications after polychemotherapy. MF history in 10 patients was 10.9 +/- 2.1 years. Stages III and IV were diagnosed in 2 of 10 patients. All the patients had typical pathohistological changes. Polymerase chain reaction test detected clone by rearrangement of gamma-chain of T-cell receptor. In 2 patients IPT detected CD4 absence in the presence of CD8 and CD7. The aberrant clone typical for NK-cells was detected in one case. Two patients died of the disease progression after 7 and 20 years of MF.
Multiple tests help early diagnosis and conduction of optimal therapy for cutaneous T-cell lymphomas.
尝试采用联合方法研究原发性皮肤T细胞淋巴瘤的临床形态学和免疫表型特征。
对1998年至2004年在血液学研究中心接受治疗的7例蕈样肉芽肿病(SD)患者(4例男性,3例女性,平均年龄53.1±7.8%)和10例蕈样霉菌病(MF)患者(6例男性,4例女性,平均年龄54.0±4.0岁)的临床、组织学、基因和免疫表型参数进行了研究。
7例SD患者中有6例处于SD IV期并伴有白血病化,外周血中发现了蕈样肉芽肿细胞。5例患者观察到骨髓和淋巴结受累。3例患者检测到向淋巴肉瘤转化的形态学迹象。所有患者的皮肤样本均显示表皮趋向性,真皮和皮肤附属器有淋巴细胞浸润。所有患者的T细胞受体γ链均有克隆重排。免疫表型分析(IPT)在淋巴细胞上检测到T细胞标志物CD45RO、CD43、CD3、CD4。3例患者外周血淋巴细胞的IPT具有SD的典型特征。1例患者检测到CD4和CD2、CD4和CD5密度低,1例患者检测到CD7存在。病程为3.4±0.7年。致死结局与多药化疗后的败血症并发症有关。10例MF患者的病程为10.9±2.1年。10例患者中有2例被诊断为III期和IV期。所有患者均有典型的病理组织学改变。聚合酶链反应检测通过T细胞受体γ链重排检测到克隆。2例患者的IPT在存在CD8和CD7的情况下检测到CD4缺失。1例患者检测到典型的NK细胞异常克隆。2例MF患者在病程7年和20年后死于疾病进展。
多项检测有助于皮肤T细胞淋巴瘤的早期诊断和最佳治疗的实施。