Department of Pathology, Duke University Medical Center, Durham, NC 27710, USA.
Int J Gynecol Pathol. 2010 Mar;29(2):173-80. doi: 10.1097/PGP.0b013e3181bb4f05.
Granular cell tumors (GCTs) are benign Schwann cell-derived neoplasms occurring throughout the body. Vulvar GCTs are usually isolated, but occasionally multifocal. On account of their anatomic location, surgical interventions aiming for negative resection margins can result in significant morbidity. We describe the clinicopathologic features of 17 vulvar GCTs in 13 patients followed for an average of 7 years. The average age at presentation was 46 years, and 84% of the patients were black. The tumors were multifocal in 3 (23%) patients, and all, either at presentation or subsequently also developed extravulvar foci. Patients with multifocal vulvar GCTs were nearly 10 years younger at presentation than patients in whom the disease was isolated. The most common complaint was a slow-enlarging mass occasionally associated with pruritus or overlying hyperpigmentation. Clinically, the tumors were subcutaneous, mobile, and nodular (2.1 cm on average), without overlying ulceration, and most often were found in the labia majora (6/17). The neoplasms were histologically heterogeneous, but exhibited either a predominantly nodular (3/17) or infiltrative (13/17) pattern of invasion. Cytologically, the tumors displayed round to polygonal cells with a granular cytoplasm, small hyperchromatic nuclei with minimal pleomorphism, and less than 2 mitoses per 10 high power fields. One tumor (1/17) consisted of cells with predominantly vesicular nuclei and prominent nucleoli and was classified as an atypical vulvar GCT. All tumors so examined were reactive for S-100 protein. Eight of 17 tumor excision specimens had positive margins. Of these, 5 tumors remained stable whereas the other 2 with follow-up progressed to require reexcisions after periods of 14 and 8.0 years, respectively. All patients with excisions with negative margins remained stable. Patients with multifocal tumors did not have a higher risk of recurrence per tumor, compared with patients with isolated disease, regardless of the margin status. No patient died from her disease. As granular cell neoplasms have such a low risk or recurrence and behave generally in an indolent manner, aggressive therapy is usually unwarranted.
颗粒细胞瘤(GCT)是一种良性雪旺氏细胞来源的肿瘤,可发生于全身各处。外阴 GCT 通常为单发,但偶尔也会多发。由于其解剖位置,为了获得阴性切缘,手术干预可能会导致严重的发病率。我们描述了 13 例患者的 17 例外阴 GCT 的临床病理特征,这些患者的平均随访时间为 7 年。发病时的平均年龄为 46 岁,84%的患者为黑人。3 例(23%)患者为多发病灶,所有患者在发病时或随后均出现外阴外病灶。多发病灶的患者比单发患者年轻近 10 岁。最常见的主诉是缓慢增大的肿块,偶尔伴有瘙痒或色素沉着过度。临床上,肿瘤为皮下、可移动的结节状(平均 2.1cm),无溃疡,最常发生于大阴唇(17/17)。肿瘤的组织学表现多样,但具有明显的结节状(17/17)或浸润性(13/17)生长方式。细胞学上,肿瘤显示出圆形到多边形的细胞,具有颗粒状细胞质,小而深染的核,轻度多形性,每 10 个高倍视野中少于 2 个有丝分裂象。1 例肿瘤(1/17)主要由具有泡状核和显著核仁的细胞组成,被归类为不典型外阴 GCT。所有检查的肿瘤均对 S-100 蛋白呈阳性反应。17 例肿瘤切除标本中有 8 例切缘阳性。其中,5 例肿瘤保持稳定,而另外 2 例有随访,分别在 14 年和 8.0 年后进展,需要再次切除。所有切缘阴性的患者均保持稳定。与单发疾病相比,多发病灶的患者无论切缘状态如何,每例肿瘤的复发风险均无升高。没有患者死于该病。由于颗粒细胞瘤的复发风险如此之低,且通常表现为惰性,因此通常不需要激进的治疗。