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表现为腺性分化的周围神经肿瘤(腺性施万瘤)。

Peripheral nerve tumors showing glandular differentiation (glandular schwannomas).

作者信息

Woodruff J M

出版信息

Cancer. 1976 May;37(5):2399-413. doi: 10.1002/1097-0142(197605)37:5<2399::aid-cncr2820370532>3.0.co;2-2.

Abstract

Five unusual peripheral nerve tumors of a type originally described by Garrè in 1892 are reported. Each showed unique foci of glandular differentiation. Foci of cartilage were seen in two cases, one of which also showed osteoid. Three of the patients had von Recklinghausen's disease. All but one of the cases showed glands lined by nonciliated cuboidal and/or pseudostratified columnar epithelium bearing clear cytoplasm and demonstrating mucin production. Goblet cells were formed in two cases. While the glandular components appeared malignant in none of the tumors, the spindle-cell element in four of five cases was considered histologically malignant. Three of the patients died with clinical evidence of recurrent or metastatic disease. The first reported examples of this tumor also arose in patients with von Recklinghausen's disease. Data from our five cases and two cases in the literature indicate that glandular schwannomas are potentially malignant tumors with a wide survival span. Follow-up showed that of seven patients, four died with clinical evidence of disease within 7 months to 10 years of their diagnosis. The remaining three were alive and free of disease after 4, 5 and 10 1/2 years. Outcome in a given case is probably related to the degree of malignant change demonstrated by the spindle-cell component of the tumor.

摘要

本文报告了5例罕见的周围神经肿瘤,其最初由加雷于1892年描述。每例均显示出独特的腺性分化灶。2例可见软骨灶,其中1例还显示类骨质。3例患者患有冯·雷克林豪森病。除1例病例外,其余所有病例均显示腺体由无纤毛的立方上皮和/或假复层柱状上皮衬里,这些上皮细胞含有透明细胞质并显示有粘蛋白分泌。2例形成杯状细胞。虽然在所有肿瘤中腺性成分均未显示为恶性,但5例中的4例的梭形细胞成分在组织学上被认为是恶性的。3例患者死于复发或转移性疾病的临床证据。该肿瘤的首例报道病例也发生在患有冯·雷克林豪森病的患者中。我们5例病例以及文献中的2例病例的数据表明,腺性神经鞘瘤是具有广泛生存跨度的潜在恶性肿瘤。随访显示,7例患者中,4例在诊断后7个月至10年内死于疾病的临床证据。其余3例在4年、5年和10.5年后仍存活且无疾病。特定病例的预后可能与肿瘤梭形细胞成分所显示的恶性变化程度有关。

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