Multiple angina bullosa haemorrhagica like oropharyngeal lesions associated with severe acute respiratory syndrome coronavirus 2-induced immune thrombocytopenia: A rare case report

M. Kaur, Virender Gombra, Apoorva Rana, S. Hasan
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Abstract

Rationale: Angina bullosa hemorrhagica (ABH) or blood blisters have an acute onset and occur independently of other disturbances of the human body like vesiculo-bullous disorders, vascular disorders, systemic causes etc. ABH is sometimes painful in the oral cavity, most commonly affects the soft palate and less commonly affects the masticatory mucosa. Within a short period of time, these blood filled lesions burst spontaneously resulting in superficial erosions and healing without scarring within 1-2 weeks. ABH has a good prognosis and the only complication reported in the literature has been of airway obstruction. Patient Concerns: A 50 yr old female patient presented with the chief complaint of blood filled blisters and bleeding gums since one week. Diagnosis: Blood filled blisters were noted at multiple sites in the oral mucosa. Blood investigation revealed mild alteration in platelet count and endoscopy displayed involvement of the pharyngeal mucosa. A provisional diagnosis of ABH-like lesion as a covid -19 related delayed inflammatory reaction to LA was given. Interventions: Symptomatic management with topical agents was done. Outcomes: The lesions had completely healed by the seventh day and she remains symptom free eight months post episode. Lessons: The presented case is a very rare condition affecting the oral cavity and involvement of the pharyngeal mucosa additionally in a post COVID-19 patient is even more rare. A delayed inflammatory reaction to LA due to exposure to the SARS-COV-2 spike protein and dysregulation in immune function associated with immune thrombocytopenia (ITP) are postulated in this case of ABH-like lesions involving the oro-pharyngeal mucosa. It is very important to be clinically observant in recovered covid 19 patients too for atypical presentations.
冠状病毒2型致免疫性血小板减少症合并多发性大疱性心绞痛出血样口咽病变1例罕见报告
理由:大疱性心绞痛出血(ABH)或血泡具有急性发作性,独立于其他人体紊乱发生,如大疱性膀胱疾病、血管疾病、全身原因等。ABH有时口腔疼痛,最常见的影响软腭,较少影响咀嚼粘膜。在短时间内,这些充满血液的病变会自发破裂,导致浅表侵蚀,并在1-2周内愈合,没有疤痕。ABH预后良好,文献中报道的唯一并发症是气道阻塞。患者关注:一名50岁的女性患者自一周以来主要主诉为充血性水泡和牙龈出血。诊断:口腔粘膜多处可见充血性水疱。血液检查显示血小板计数有轻微改变,内窥镜检查显示咽部黏膜受累。初步诊断ABH样病变为新冠肺炎-19相关的LA延迟炎症反应。干预措施:使用局部药物进行症状处理。结果:病变在第七天完全愈合,发作后八个月她仍然没有症状。经验教训:本病例是一种非常罕见的影响口腔的疾病,新冠肺炎后患者的咽粘膜受累更为罕见。在这种涉及口咽粘膜的ABH样病变的情况下,假设由于暴露于严重急性呼吸系统综合征冠状病毒2型刺突蛋白和与免疫性血小板减少症(ITP)相关的免疫功能失调而导致对LA的延迟炎症反应。对19名新冠肺炎康复患者进行临床观察对于非典型表现也非常重要。
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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