Spontaneous Lingual Bleeding and Intracerebral Hemorrhage in a Young Adult with Immune Thrombocytopenia (ITP): A Rare Case Report and Brief Recent Update on Treatment.

Jitendra Singh, Anju Dinkar, Nilesh Kumar, Kailash Kumar, Ravi Ranjan, Isha Atam
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Abstract

Introduction: Immune thrombocytopenia (ITP) is an autoimmune condition characterized by reduced platelet counts due to increased peripheral destruction and impaired platelet generation. An estimated incidence of ITP is 2 to 5 cases per 100,000 individuals in the general population. While mucocutaneous bleeding is common, life-threatening complications, such as spontaneous lingual hematoma and intracerebral hemorrhage (ICH), are extremely rare. Rapid progression of lingual haematomas might compromise airway function and necessitate immediate medical intervention. It is well established that most patients with ITP respond to first-line therapy; however, severe bleeding events, such as intracerebral hemorrhage, occur in less than 1% of cases and are associated with significant morbidity and mortality.

Case presentation: A 21-year-old male with a 6-month history of chronic ITP and poor compliance with therapy presented with a 2-day history of progressive reddish discoloration and swelling of the tongue. The clinical examination revealed stable vital signs and a remarkable general and systemic evaluation. The relevant blood routine showed a critically low platelet count at 8×103/μL, with normal coagulation parameters. No other bleeding manifestations were noted. Four hours after admission, the patient developed generalized tonic-clonic seizures and altered sensorium. Computed tomography (CT) of the head revealed an ICH. He was managed with single- donor platelet transfusions, intravenous anti-epileptics, pulse corticosteroid therapy, eltrombopag, and supportive care. The patient demonstrated a favorable clinical response, characterized by a rising platelet count and resolution of symptoms. He was discharged in stable condition with counseling on therapy adherence.

Conclusion: The present case emphasizes the rarely yet life-threatening complication of inadequately managed ITP, such as spontaneous lingual hematoma and intracranial haemorrhage. It highlights the vital significance of therapy adherence and timely interdisciplinary intervention to avert disastrous consequences. Timely detection and intervention are crucial for positive outcomes in these intricate cases.

自发性舌出血和脑出血的年轻人与免疫性血小板减少症(ITP):一个罕见的病例报告和简短的最新治疗进展。
免疫性血小板减少症(ITP)是一种自身免疫性疾病,其特征是由于外周破坏增加和血小板生成受损导致血小板计数减少。在一般人群中,ITP的估计发病率为每10万人2至5例。虽然皮肤粘膜出血是常见的,但危及生命的并发症,如自发性舌血肿和脑出血(ICH),是极其罕见的。舌血肿的快速发展可能损害气道功能,需要立即进行医疗干预。众所周知,大多数ITP患者对一线治疗有反应;然而,严重出血事件,如脑出血,发生在不到1%的病例中,并与显著的发病率和死亡率相关。病例介绍:21岁男性,慢性ITP病史6个月,治疗依从性差,2天进行性红变和舌肿。临床检查显示生命体征稳定,全身评价良好。相关血常规显示血小板计数极低,8×103/μL,凝血参数正常。未见其他出血表现。入院后4小时,患者出现全身性强直阵挛性发作和感觉改变。头部计算机断层扫描(CT)显示脑出血。他接受了单供体血小板输注、静脉注射抗癫痫药物、脉冲皮质类固醇治疗、伊曲波巴和支持性护理。患者表现出良好的临床反应,其特点是血小板计数上升和症状消退。出院时病情稳定,并接受治疗依从性咨询。结论:本病例强调了ITP治疗不当的罕见但危及生命的并发症,如自发性舌血肿和颅内出血。它强调了治疗依从性和及时的跨学科干预以避免灾难性后果的重要意义。及时发现和干预对于这些复杂病例的积极结果至关重要。
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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