Mature Type T-Lymphoblastic Leukemia/Lymphoma Presenting With Isolated Central Nervous System Symptomatology in a Patient With Giant Cell Arteritis on Long-Term Steroid Treatment.
John Kolton Smith, Xinmin Zhang, Stephen C Machnicki, Salman Azhar, Morana Vojnic
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引用次数: 0
Abstract
T-lymphoblastic leukemia/lymphoma (T-ALL/T-LBL) is a malignancy comprised of T-lymphoblasts that can present as one of four clinical subtypes (pro-T, pre-T, cortical T, and mature T). Clinical presentation is typically characterized by leukocytosis with diffuse lymphadenopathy and/or hepatosplenomegaly. Beyond clinical presentation, specific immunophenotypic and cytogenetic classifications are utilized to diagnose mature T-ALL. In later disease stages it can spread to the central nervous system (CNS); however, presentation of mature T-ALL by way of CNS pathology and clinical symptomatology alone is rare. Even more rare is the presence of poor prognostic factors without correlating significant clinical presentation. We present a case of mature T-ALL in an elderly female with isolated CNS symptoms in combination with poor prognostic factors including terminal deoxynucleotidyl transferase (TdT) negativity and a complex karyotype. Our patient lacked the classical symptomatology and laboratory findings of mature T-ALL but deteriorated quickly upon diagnosis due to the aggressive genetic profile of her cancer.
T淋巴母细胞白血病/淋巴瘤(T- all /T- lbl)是一种由T淋巴母细胞组成的恶性肿瘤,可表现为四种临床亚型(前T、前T、皮质T和成熟T)之一。临床表现典型特征为白细胞增多伴弥漫性淋巴结病和/或肝脾肿大。除了临床表现,特异性免疫表型和细胞遗传学分类被用于诊断成熟T-ALL。在疾病晚期,它可以扩散到中枢神经系统(CNS);然而,仅通过中枢神经系统病理和临床症状来表现成熟T-ALL是罕见的。更罕见的是存在不良的预后因素而没有显著的临床表现。我们报告一例成熟的T-ALL在老年女性与孤立的中枢神经系统症状,结合不良的预后因素,包括终端脱氧核苷酸转移酶(TdT)阴性和复杂的核型。我们的患者缺乏成熟T-ALL的典型症状和实验室结果,但由于其癌症的侵袭性遗传特征,诊断后病情迅速恶化。