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Synchronous subcutaneous granular cell tumours a rare presentation

机译:同步皮下颗粒细胞瘤罕见的表现

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摘要

We describe a unique presentation of a rare disease presentation of a granular cell tumour. A 36-year-old woman presents with a large symptomatic left flank mass that had been slowly increasing in size. Multiple synchronous subcutaneous masses were found at presentation on the left breast, right auricle and right cheek. After diagnosis of granular cell tumour by core needle biopsy, the masses were excised with histopathological and immunohistochemical analysis of both specimens confirming the presence of non-malignant granular cell tumours. Granular cell tumours are rare Schwann cell derived tumours that are typically asymptomatic and benign. These tumours are most often located in the head and neck, with multifocal disease present in approximately 5–16% of patients. Final pathology is necessary for diagnosis and frozen section is rarely helpful. Malignancy is present in approximately 2% of cases and can be diagnosed by the presence of a high mitotic rate, large nucleoli, necrosis, spindling and pleomorphism are other suspicious features. Granular cell tumours do not generally require adjuvant treatment. The mainstay of therapy is surgical resection with surveillance.
机译:我们描述了粒细胞瘤的罕见疾病表现的独特表现。一名36岁的女性表现出较大的症状性左胁腹肿块,并逐渐增大。左乳房,右耳廓和右脸颊处出现多个同步皮下包块。在通过核心针穿刺活检诊断为颗粒细胞瘤后,通过对两个标本进行组织病理学和免疫组织化学分析,切除肿块,确认存在非恶性颗粒细胞瘤。颗粒细胞瘤是罕见的雪旺细胞衍生肿瘤,通常无症状和良性。这些肿瘤最常见于头颈部,约有5-16%的患者患有多灶性疾病。最终病理对于诊断是必要的,冷冻切片几乎没有帮助。大约2%的病例存在恶性肿瘤,可以通过存在高有丝分裂率来诊断,核仁大,坏死,多刺和多形性是其他可疑特征。颗粒细胞肿瘤通常不需要辅助治疗。治疗的主要手段是手术切除并进行监视。

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