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.

IF 1.3 Q4 HEMATOLOGY Journal of hematology Pub Date : 2023-02-01 DOI:10.14740/jh1037
John Kolton Smith, Xinmin Zhang, Stephen C Machnicki, Salman Azhar, Morana Vojnic
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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.

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成熟型t淋巴母细胞白血病/淋巴瘤在长期类固醇治疗的巨细胞动脉炎患者中表现出孤立的中枢神经系统症状。
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。
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Journal of hematology
Journal of hematology HEMATOLOGY-
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