小儿外耳道血管平滑肌瘤1例报告。

IF 0.4 Q4 OTORHINOLARYNGOLOGY
Case Reports in Otolaryngology Pub Date : 2025-06-15 eCollection Date: 2025-01-01 DOI:10.1155/crot/1538233
Wm Zachary Salter, Kolos K Nagy, Drew H Smith, Arif Dauod, Tam Q Nguyen
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引用次数: 0

摘要

血管平滑肌瘤(ALM)是平滑肌瘤的一种亚型,其特征是血管受累以及平滑肌细胞的增殖。这些肿瘤通常发生在下肢,很少发生在头颈部。在此,我们报告一例罕见的外耳道ALM (EAC),发生于一名12岁的女性。据我们所知,这是EAC报告的第6例和第2例最年轻的ALM患者。最初,该患者被诊断为外耳炎伴息肉样变,并开了一个疗程的环丙醇。随访CT显示右侧EAC软组织密度,符合内侧管纤维化,计划在麻醉下检查并局部切除肿块。手术结果显示,在鼓膜外侧的EAC胆脂瘤的同时,仔细地切除了一个起源于圣托里尼裂缝的软骨状、坚固的肿块。Huschke孔未受累,鼓膜完整,无穿孔。最终病理证实为良性ALM。EAC用氟辛浸透的明胶泡沫包装,放置2周,并指导每天放置氟辛滴剂。一旦明胶泡沫在临床上被移除,EAC被发现愈合良好,患者注意到主观听力的改善。在5个月的时间里没有任何复发。这个病例记录了一个罕见的ALM在一个极其罕见的解剖位置,成功地管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Angioleiomyoma of the External Auditory Canal in a Pediatric Patient: A Case Report.

Angioleiomyoma (ALM) is a subtype of leiomyoma characterized by vascular involvement alongside the proliferation of smooth muscle cells. These tumors are generally found in the lower limb and rarely occur in the head and neck region. Herein, we present a rare case of ALM of the external auditory canal (EAC) in a 12-year-old female. To our knowledge, this is the sixth case and the second youngest patient reported with ALM occurring in the EAC. Initially, this patient was diagnosed with otitis externa with polypoid change and prescribed a course of Ciprodex. Follow-up CT demonstrated a soft tissue density in the right EAC, consistent with medial canal fibrosis, and an exam under anesthesia with local excision of the mass was scheduled. Surgical findings showed a cartilaginous, firm mass originating from the fissure of Santorini that was carefully excised completely along with an EAC cholesteatoma seen lateral to the tympanic membrane. The foramen of Huschke was uninvolved and the tympanic membrane was intact without perforation. Final pathology confirmed benign ALM. The EAC was packed with floxin-soaked gelfoam and left packed for 2 weeks with instructions for daily floxin drop placement. Once the gelfoam was removed in the clinic, the EAC was found to be healing well and the patient noted improved subjective hearing. There has not been any subsequent recurrence over a period of 5 months. This case documents a rare presentation of an ALM in an extremely rare anatomical position which was managed successfully.

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来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
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审稿时长
13 weeks
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