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表现为坏死性外耳道炎的颞骨髓系肉瘤:一例报告及文献综述

Temporal Bone Myeloid Sarcoma Presenting as Necrotizing Otitis Externa: A Case Report and Literature Review.

作者信息

Nayouf Oubai, Alahmad Molham, Laflouf Miriam, Alhammod Abduljaleel, Sulaiman Ameen, Yousfan Abdulmajeed

机构信息

Faculty of Medicine, Damascus University, Damascus, Syria.

Department of Otolaryngology-Head and Neck Surgery, Al-Mouwasat University Hospital, Faculty of Medicine, Damascus University, Damascus, Syria.

出版信息

Ear Nose Throat J. 2024 Oct 27:1455613241293870. doi: 10.1177/01455613241293870.

Abstract

Myeloid sarcoma (MS) is a proliferation of immature myeloid cells that occurs extramedullary, often accompanying acute myeloid leukemia (AML). It typically presents in areas such as lymph nodes, skin, and the head and neck regions. The emergence of MS within the temporal bone is rare, and it can manifest through nonspecific symptoms. In this paper, we reported a case of A 47-year-old female presented with right-sided otalgia, otorrhea, tinnitus, reduced hearing, and ear fullness, and developed facial asymmetry. She was initially diagnosed with necrotizing otitis externa and was treated accordingly. Further investigations were conducted, leading to the diagnosis of MS. She began treatment with induction chemotherapy followed by consolidation therapy. And we reviewed the literature and included 14 MS cases with the same anatomical localization, discussing the primary presentation, immunohistochemistry, and treatment approaches of these patients. In conclusion, temporal bone MS should be considered in patients with a history of AML presenting with nonspecific symptoms. Diagnostic modalities for MS include computed tomography and magnetic resonance imaging scans. Systemic chemotherapy remains the preferred treatment approach. The complexity and diversity of temporal bone MS presentations necessitate further comprehensive research to enhance understanding and improve management strategies for this rare condition.

摘要

髓系肉瘤(MS)是未成熟髓系细胞的增殖,发生于髓外,常伴有急性髓系白血病(AML)。它通常出现在淋巴结、皮肤以及头颈部等部位。颞骨内出现MS较为罕见,可通过非特异性症状表现出来。在本文中,我们报告了一例47岁女性,她出现右侧耳痛、耳漏、耳鸣、听力下降和耳闷,并出现面部不对称。她最初被诊断为坏死性外耳道炎并接受了相应治疗。进一步检查后,诊断为MS。她开始接受诱导化疗,随后进行巩固治疗。我们回顾了文献,纳入了14例具有相同解剖定位的MS病例,讨论了这些患者的主要表现、免疫组化和治疗方法。总之,有AML病史且出现非特异性症状的患者应考虑颞骨MS。MS的诊断方法包括计算机断层扫描和磁共振成像扫描。全身化疗仍然是首选的治疗方法。颞骨MS表现的复杂性和多样性需要进一步全面研究,以增进对这种罕见疾病的了解并改善管理策略。

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