Multifaceted Clinical Spectrum of Vitamin B12 Deficiency - a Case Report and Literature Review.

IF 2.7 Q3 HEMATOLOGY
Journal of Blood Medicine Pub Date : 2025-08-25 eCollection Date: 2025-01-01 DOI:10.2147/JBM.S524466
Ewa Pustelnik, Katarzyna Pikora, Magdalena Zofia Hartman, Marta Kurzeja, Joanna Czuwara, Paweł Łaguna
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引用次数: 0

Abstract

Background: Vitamin B12 (cobalamin) deficiency is a well-known cause of hematologic and neurological disorders; however, its presentation can be highly variable, leading to diagnostic challenges. The etiology is diverse: while the most common cause is dietary insufficiency, other potential causes include malabsorption syndromes, autoimmune gastritis, gastrointestinal disorders, chronic infections, and genetic defects. Clinical presentation varies significantly, ranging from clinically silent macrocytosis to life-threatening anemia or pancytopenia. Neurological and psychiatric manifestations may include vision and gait impairment, depression, and cognitive dysfunction. Given this complexity, vitamin B12 deficiency can mimic other conditions, often leading to a delay in diagnosis.

Case presentation: A 15-year-old male was admitted in critical condition with severe anemia, thrombocytopenia, jaundice, progressive weight loss, fatigue, gait disturbances, and vision impairment. Initially, Evan's syndrome was suspected, but further laboratory investigations, including a peripheral blood smear and elevated mean corpuscular volume (MCV), led to the diagnosis of profound vitamin B12 deficiency. Additional workup revealed chronic atrophic gastritis as the underlying cause. The patient was treated with vitamin B12 injections, leading to significant hematologic and neurological improvement, weight gain, and resolution of psychiatric symptoms. However, optic nerve atrophy was detected as a late complication.

Conclusion: This case emphasizes the need to consider vitamin B12 deficiency in pediatric patients with unexplained hematologic, neurological, and psychiatric symptoms, particularly when associated with chronic atrophic gastritis. Early recognition and intervention are crucial to preventing irreversible complications, such as optic neuropathy. Given the multidisciplinary nature of its presentation, this case serves as an important reminder for pediatricians, hematologists, gastroenterologists, and neurologists to maintain a high index of suspicion for vitamin B12 deficiency in complex clinical scenarios.

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维生素B12缺乏症的多方面临床谱-一个病例报告和文献综述。
背景:维生素B12(钴胺素)缺乏是血液学和神经系统疾病的一个众所周知的原因;然而,它的表现可能是高度可变的,导致诊断的挑战。病因多种多样:最常见的原因是饮食不足,其他潜在原因包括吸收不良综合征、自身免疫性胃炎、胃肠道疾病、慢性感染和遗传缺陷。临床表现差异很大,从临床沉默的巨细胞增多到危及生命的贫血或全血细胞减少。神经和精神方面的表现可能包括视力和步态障碍、抑郁和认知功能障碍。鉴于这种复杂性,维生素B12缺乏症可以模仿其他疾病,经常导致诊断延误。病例介绍:一名15岁男性因严重贫血、血小板减少、黄疸、进行性体重减轻、疲劳、步态障碍和视力障碍而入院,病情危重。最初,埃文综合征被怀疑是可能的,但进一步的实验室检查,包括外周血涂片和平均红细胞体积(MCV)升高,导致诊断为严重的维生素B12缺乏症。进一步的检查显示慢性萎缩性胃炎是潜在的病因。患者接受维生素B12注射治疗,导致血液学和神经学显著改善,体重增加,精神症状缓解。然而,视神经萎缩被发现为晚期并发症。结论:本病例强调有不明原因血液学、神经学和精神病学症状的儿科患者需要考虑维生素B12缺乏症,特别是与慢性萎缩性胃炎相关的儿童患者。早期识别和干预对于预防不可逆转的并发症(如视神经病变)至关重要。鉴于其表现的多学科性质,该病例对儿科医生、血液学家、胃肠病学家和神经科医生在复杂的临床情况下保持对维生素B12缺乏症的高度怀疑起到重要的提醒作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
94
审稿时长
16 weeks
期刊介绍: The Journal of Blood Medicine is an international, peer-reviewed, open access, online journal publishing laboratory, experimental and clinical aspects of all topics pertaining to blood based medicine including but not limited to: Transfusion Medicine (blood components, stem cell transplantation, apheresis, gene based therapeutics), Blood collection, Donor issues, Transmittable diseases, and Blood banking logistics, Immunohematology, Artificial and alternative blood based therapeutics, Hematology including disorders/pathology related to leukocytes/immunology, red cells, platelets and hemostasis, Biotechnology/nanotechnology of blood related medicine, Legal aspects of blood medicine, Historical perspectives. Original research, short reports, reviews, case reports and commentaries are invited.
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