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Epithelioid Schwannomas: An Analysis of 58 Cases Including Atypical Variants.

包括不典型亚型在内的58例上皮样神经鞘瘤分析

Hart J,Gardner JM,Edgar M,Weiss SW

Abstract

The histologic features and outcome of 58 cases of epithelioid schwannoma were studied to determine the significance of atypical histologic features. Cases were retrieved from personal consultation files from 1999 to 2013. Patients (31 male and 26 female patients) ranged in age from 14 to 80 years (median, 38 y). Two patients had schwannomatosis 1. Tumors developed in the dermis/subcutis (n=56) or muscle (n=2) of the upper extremity (34.5%), lower extremity (34.5%), thorax/abdomen/back (18%), and less common anatomic locations including the scalp, neck, lip, and breast. They ranged in size from 0.25 to 4.5 cm (median, 2.0 cm). Typically circumscribed and surrounded by a perineurium, they comprised single or small groups of epithelioid schwann cells with a moderate amphophilic cytoplasm and occasional nuclear pseudoinclusions. Stroma varied from myxoid to hyalinized, often with thick-walled vessels (55 cases). Mitotic rate ranged from 0 to 9 mitoses/10 high-power field (HPF) (2.37 mm) in the most active areas (mean, 2 to 3 mitoses/10 HPFs). Thirteen cases (22%) were "atypical," defined by a high mitotic rate (≥3 mitoses per 10 HPFs) and nuclear size variation (≥3:1). All (56/56) expressed S100 protein; type IV collagen invested groups or individual cells (16/17). Melanoma markers were negative, except for melan A (1 case). Follow-up in 39 patients (median, 78 mo; range, 6 to 174 mo) indicated that 31 (79%) were alive without disease (including 9/13 atypical cases; median, 78 mo), 7 (18%) were alive with unknown status, and 1 patient had died of unrelated causes. One tumor recurred, but none metastasized. Epithelioid schwannomas, even those with atypical features, are benign and do not constitute a histologic continuum with epithelioid malignant peripheral nerve sheath tumors, which typically occur in deep soft tissues and have more anaplastic features.

摘要

作者研究了58例上皮样神经鞘瘤的组织学特征和患者的临床结局,来阐述不典型组织学特征在上皮样神经鞘瘤中的意义。病例来自19992013年期间的会诊病例。男性31例,女性26例;年龄1480岁(中位年龄38岁);2例患者伴有1型神经纤维瘤病。肿瘤发生在真皮/皮下组织(n=56)或肌肉内(n=2),其中上肢(34.5%)、下肢(34.5%)、胸部/腹部/背部(18%)及其它一些少见的解剖位点(包括头皮、颈部、口唇和乳腺)。肿瘤直径0.254.5 cm (中位直径2.0 cm),典型者肿瘤边界清楚,被神经束膜包绕,由单一的或小的成群上皮样神经鞘细胞构成,具有温和的嗜双色性胞浆,偶尔可见核内假包涵体;间质为黏液样或透明变基质,厚壁血管常见(n=55);最活跃区域的核分裂像09/10 HPF(2.37 mm) (平均23个核分裂像/10 HPFs)13例(22%)具有高核分裂率(≥3核分裂像/ 10HPFs)和核大小变化(≥3:1)的病例,诊断为不典型上皮样神经鞘瘤。全部(56/56)病例表达S100蛋白;部分病例(16/17)弥漫表达IV型胶原;除1melan A阳性外,其余病例黑色素标记物均阴性。39例获得随访(随访时间6174个月,中位随访时间78个月),其中31例(79%)无病生存(包括9/13不典型病例,中位随访时间78个月);7例(18%)存活,但身体状况未知;1例死于与之无关的疾病;1例复发,但均未见转移。总之,上皮样神经鞘瘤,甚至具有不典型特征的,仍然是一种良性肿瘤,与上皮样恶性外周神经鞘膜瘤并不构成一个连续的组织学谱系,后者主要发生在深部软组织,并且具有更多的间变性特征。

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