Hassan Abdulahi, Simpson Matthew, Jiwani Rahim, Arrigo Abigail, Nisarga Palgun, Esan Olukemi A, Koget Anna
Allegheny General Hospital, Department of Internal Medicine, Pittsburgh, PA, USA.
Allegheny General Hospital, Department of Hematology & Oncology, Pittsburgh, PA, USA.
J Community Hosp Intern Med Perspect. 2024 Sep 9;14(5):96-100. doi: 10.55729/2000-9666.1389. eCollection 2024.
Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) is a rare hematologic cancer, accounting for less than 1% of acute leukemias in the U.S. Diagnosis involves detecting markers like CD123, CD4, CD56, TCL1, and TCF4. Treatment typically involved acute leukemia therapies, but Tagraxofusp, a targeted therapy, was recently approved. Despite advancements, prognosis remains grim, with a median survival of around 1 year. Atraumatic splenic rupture (ASR) is a rare complication of this condition, with only five cases reported from 1994 to 2018. Here we present a case of BPDCN complicated by ASR. This case emphasizes the challenges of diagnosing and treating BPDCN, noting its rarity and absence of standard therapy. Tagraxofusp has shown promising results but presents safety concerns like capillary leak syndrome, particularly in elderly patients with comorbidities.
母细胞性浆细胞样树突状细胞肿瘤(BPDCN)是一种罕见的血液系统癌症,在美国占急性白血病的比例不到1%。诊断包括检测如CD123、CD4、CD56、TCL1和TCF4等标志物。治疗通常采用急性白血病疗法,但靶向疗法塔格昔单抗最近已获批准。尽管有进展,但预后仍然严峻,中位生存期约为1年。非创伤性脾破裂(ASR)是这种疾病的一种罕见并发症,1994年至2018年仅有5例报告。在此,我们报告一例并发ASR的BPDCN病例。该病例强调了诊断和治疗BPDCN的挑战,指出其罕见性以及缺乏标准疗法。塔格昔单抗已显示出有前景的结果,但存在如毛细血管渗漏综合征等安全问题,尤其是在患有合并症的老年患者中。