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首页> 外文期刊>Journal of Clinical and Diagnostic Research >A Case of Bone Marrow Necrosis of an Idiopathic Aetiology: The Report of a Rare Entity with Review of the Literature
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A Case of Bone Marrow Necrosis of an Idiopathic Aetiology: The Report of a Rare Entity with Review of the Literature

机译:一例特发性病因的骨髓坏死病例:文献报道的罕见病报告。

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摘要

Bone Marrow Necrosis (BMN) is regarded as a rare entity in the aspirates and the trephine biopsies which are obtained from living patients and it is a rare antemortem diagnosis. Usually, BMN is associated with a poor prognosis and it has a 90% association with malignancies (mainly haematological). Its other causes include infections, drugs and other non malignant haematological causes. BMN which occurs due to unknown causes (idiopathic), is very rare. The present case report describes a case of BMN in a 14 year old male child from rural background, who came to the medicine outpatient department of a tertiary care centre in north India, with the complaints of generalized weakness, severe bone pains, especially in the ribcage area and fatigue. His peripheral blood film revealed pancytopaenia. His bone marrow aspiration yielded a watery, sero-sanguinous fluid from 2 different sites. Microscopy revealed ?ghost like? haematopoietic cells lying in eosinophilic, proteinaceous material. Bone marrow biopsies from both the sites revealed extensive foci of gelatinous transformation and necrosis. A diagnosis of BMN was rendered. No underlying neoplastic / non neoplastic cause was identified, even after a thorough systematic investigation (haematological/biochemical/ radiological and immunological). Thus, a final diagnosis of BMN due to an idiopathic cause, was finally given. The patient was given supportive treatment, after which he was referred to a higher centre. BMN which arises idiopathically is usually very rare and often precedes the aetiological diagnosis and obscures the diagnosis. Traditionally, the prognoses of the patients with BMN were considered as poor, but with better treatment aids (chemotherapy and supportive treatment), the prognoses of these patients have been found to improve. Vigorous supportive care, along with a disease specific treatment, is the key to its management. This case was worth reporting, as no cause of BMN was elicited in it and we have summarized the signs and symptoms, the associations, haematological and other lab investigations and the role of radiology, which helped in its diagnosis.
机译:骨髓坏死(BMN)被认为是从活着的患者那里获得的抽吸物和曲汀活组织检查中的罕见实体,并且是罕见的死前诊断。通常,BMN与不良预后有关,并且与恶性肿瘤(主要是血液学)有90%的关联。其其他原因包括感染,药物和其他非恶性血液病学原因。由于未知原因(特发性)而发生的BMN非常罕见。本病例报告描述了一例来自农村背景的14岁男孩的BMN病例,该男孩来到印度北部一家三级医疗中心的门诊部就诊,普遍存在虚弱,严重的骨痛,尤其是在胸腔区域和疲劳。他的外周血膜显示全血细胞减少。他的骨髓穿刺术从两个不同部位产生了一种水样,血质的液体。显微镜显示“幽灵状”?位于嗜酸性蛋白物质中的造血细胞。来自两个部位的骨髓活检均显示出广泛的凝胶状转化和坏死灶。诊断为BMN。即使经过全面的系统研究(血液学/生化学/放射学和免疫学),也未发现潜在的肿瘤性/非肿瘤性原因。因此,最终给出了由于特发性原因导致的BMN的最终诊断。患者接受了支持治疗,之后被转诊至上级中心。特发性的BMN通常非常罕见,并且通常在病因学诊断之前就掩盖了诊断。传统上,BMN患者的预后被认为很差,但是有了更好的治疗辅助手段(化学疗法和支持治疗),这些患者的预后得到了改善。强有力的支持治疗以及针对疾病的治疗是其管理的关键。该病例值得报道,因为未发现BMN的病因,并且我们总结了体征和症状,相关性,血液学和其他实验室检查以及放射学的作用,有助于诊断。

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