Barzilai Geva, Schindler Yaakov, Cohen-Kerem Raanan
Department of Otolaryngology-Head and Neck Surgery, Carmel Medical Center, Haifa, Israel.
Ear Nose Throat J. 2009 Mar;88(3):831-2.
Angiomyomatous hamartomas have been found almost exclusively in the inguinal and femoral lymph nodes; few reports of these lesions in the head and neck region have been published. We present a case of angiomyomatous hamartoma in the submandibular area, a site that has not been previously reported in the literature. The mass was initially diagnosed as an enlarged lymph node. When it did not regress following broad-spectrum antibiotic treatment, the patient, a 51-year-old woman, underwent an excisional biopsy. Histopathology identified the mass as an angiomyomatous hamartoma. At follow-up 3 years and 9 months postoperatively, the patient exhibited no evidence of recurrence on physical examination and computed tomography. Even though angiomyomatous hamartoma of the head and neck is rare, we suggest that otolaryngologists include it in the differential diagnosis of head and neck masses.
血管肌性错构瘤几乎仅见于腹股沟和股淋巴结;关于头颈部这些病变的报道很少。我们报告一例发生于下颌下区的血管肌性错构瘤,该部位此前未见文献报道。该肿块最初被诊断为肿大淋巴结。在广谱抗生素治疗后未消退,患者为一名51岁女性,接受了切除活检。组织病理学检查将该肿块确定为血管肌性错构瘤。术后3年9个月的随访中,体格检查和计算机断层扫描均未发现患者有复发迹象。尽管头颈部血管肌性错构瘤罕见,但我们建议耳鼻喉科医生在头颈部肿块的鉴别诊断中考虑该病。