Cervantes F, Urbano-Ispizua A, Escoda L, Ordi J, Montserrat E, Rozman C
Escuela de Hematología Farreras Valenti, Hospital Clinic i Provincial, Barcelona.
Med Clin (Barc). 1991 Jun 1;97(1):21-3.
To investigate the frequency of the T lymphoid phenotype in the blast crisis of chronic myelocytic leukemia (CML) with positive Philadelphia chromosome (Ph) and to evaluate the major clinical and hematologic features of the patients with this phenotype.
The presence of the TdT enzyme was assessed and specific monoclonal antibodies to the different hemopoietic lines were used to evaluate blast cells in 38 patients with blast crisis during Ph-positive CML.
T lymphoid phenotype was found in three of the 38 patients, corresponding in all cases to immature T cells. In one patient, the blast crisis was the presenting feature of CML and in two the localization of the blast crisis was lymphadenopathic. In the two patients who could be followed up a favorable response to chemotherapy regimens including vincristine and prednisone was observed.
Although uncommon, T lymphoid blast crisis in CML should no longer be considered exceptional. This phenotypic finding suggests that, at least in some cases, CML originates in a pluripotential stem cell common to all hemopoietic cells, including T lymphocytes.
研究费城染色体(Ph)阳性的慢性粒细胞白血病(CML)急变期T淋巴细胞表型的出现频率,并评估具有该表型患者的主要临床和血液学特征。
对38例Ph阳性CML急变期患者的原始细胞进行TdT酶检测,并使用针对不同造血系的特异性单克隆抗体进行评估。
38例患者中有3例发现T淋巴细胞表型,所有病例均对应未成熟T细胞。1例患者以急变期为CML的首发表现,2例患者急变期的定位为淋巴结病性。在2例可随访的患者中,观察到对包括长春新碱和泼尼松在内的化疗方案有良好反应。
虽然罕见,但CML中的T淋巴细胞急变期不应再被视为特殊情况。这一表型发现表明,至少在某些情况下,CML起源于包括T淋巴细胞在内的所有造血细胞共有的多能干细胞。