Khor John, Boo Yang Liang
Internal Medicine, Hospital Sultanah Nora Ismail, Batu Pahat, MYS.
Hematology, Hospital Sultanah Aminah, Johor Bahru, MYS.
Cureus. 2025 May 8;17(5):e83724. doi: 10.7759/cureus.83724. eCollection 2025 May.
Hereditary spherocytosis (HS) is a common hereditary hemolytic anemia in which red blood cells (RBCs) assume spherocytic morphology, predisposing to easy destruction in the spleen. Diagnosis is readily made when spherocytes are demonstrated in the blood film of patients presenting with anemia, jaundice, and splenomegaly. A positive osmotic fragility test (OFT) is also supportive. However, when classical features are not seen in either blood film or OFT, diagnosis might become complicated, particularly in resource-limited settings. We report a teenager who was transitioned to the adult medical outpatient department with a diagnosis of hemolytic anemia; the etiology, however, was never identified. He has required monthly transfusions since six months of life and has developed antibodies to RBCs, secondary hemochromatosis, and gallstones. Workup for thalassemia and autoimmune causes was negative. A barrage of negative investigations ultimately led to a genetic analysis, which revealed a heterozygous mutation for the c.2671C>T (p.Arg891*) variant in the SPTA1 gene and a novel mutation for SPTA1 c.7134+5G>A (intronic). He was formally diagnosed with HS and underwent splenectomy. Post procedure, his anemia improved, and transfusion requirements steadily reduced. His sister exhibits the same heterozygous mutation for SPTA1 c.7134+5G>A (intronic), but did not have any clinical or laboratory manifestation of the disease. We postulate that this novel mutation in SPTA1 c.7134+5G>A (intronic) might play a role in determining disease severity, particularly when associated with a pathogenic variant.
遗传性球形红细胞增多症(HS)是一种常见的遗传性溶血性贫血,其中红细胞(RBC)呈现球形形态,易于在脾脏中被破坏。当在出现贫血、黄疸和脾肿大的患者血片中发现球形红细胞时,很容易做出诊断。阳性渗透脆性试验(OFT)也有支持作用。然而,当在血片或OFT中均未见到典型特征时,诊断可能会变得复杂,尤其是在资源有限的环境中。我们报告一名青少年,他被转诊至成人内科门诊,诊断为溶血性贫血;然而,病因从未明确。自6个月大以来,他每月都需要输血,并产生了针对红细胞的抗体以及继发性血色素沉着症和胆结石。地中海贫血和自身免疫性病因的检查均为阴性。一系列阴性检查最终导致进行基因分析,结果显示SPTA1基因存在c.2671C>T(p.Arg891*)变体的杂合突变以及SPTA1基因c.7134+5G>A(内含子)的新突变。他被正式诊断为HS并接受了脾切除术。术后,他的贫血得到改善,输血需求稳步减少。他的妹妹表现出相同的SPTA1基因c.7134+5G>A(内含子)杂合突变,但没有该疾病的任何临床或实验室表现。我们推测SPTA1基因c.7134+5G>A(内含子)的这种新突变可能在决定疾病严重程度方面发挥作用,特别是与致病变异相关时。