Department of General Surgery, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Department of Nursing, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Cancer Med. 2024 Aug;13(16):e70140. doi: 10.1002/cam4.70140.
Schwannoma is a rare mesenchymal tumor. In this study, we analyzed clinicopathologically 99 schwannomas.This retrospective study delves into the clinical, pathological, and immunohistochemical dimensions of abdominal schwannomas.
A cohort of 99 cases, comprising 4 malignant and 95 benign schwannomas, was meticulously examined. Clinical analysis revealed a notable gender distribution (1:1.7, male to female) and an average age of 58.5 years. The majority of cases were asymptomatic. A cohort of 99 cases, comprising 4 malignant and 95 benign schwannomas, was meticulously examined. Clinical analysis revealed a notable gender distribution (1:1.7, male to female) and an average age of 58.5 years. The majority of cases were asymptomatic. Tumor sizes ranged from 0.5 to 30 cm, with distinct locations in the stomach for most benign cases and the abdomen/small intestine for malignancies. Initial misdiagnoses were frequent. Pathological evaluations revealed distinct features, including Antoni A and B patterns, spindle cells, and lymphatic sheath structures in benign schwannomas. Malignant cases exhibited atypical cells, ulcers, and invasive growth. Immunohistochemical markers, such as S100, SOX10, and vimentin, consistently demonstrated positivity by contributing to accurate diagnoses. Treatment outcomes indicated a poor prognosis in malignant cases, with overall survival ranging from 10 to 41 months. Conversely, benign cases displayed no recurrence or metastasis during follow-up, despite atypical behaviors.
This study underscores the rarity of abdominal schwannomas and underscores the need for a comprehensive diagnostic morphology and immunohistochemistry. SOX10 emerges as a crucial and specific marker for accurate diagnosis. Further research is imperative to refine diagnostic protocols and enhance our understanding of the clinical behavior of abdominal schwannomas.
神经鞘瘤是一种罕见的间叶性肿瘤。本研究分析了 99 例神经鞘瘤的临床病理特征。本回顾性研究深入探讨了腹部神经鞘瘤的临床、病理和免疫组织化学特征。
仔细检查了 99 例病例,包括 4 例恶性和 95 例良性神经鞘瘤。临床分析显示出明显的性别分布(1:1.7,男性对女性)和平均年龄为 58.5 岁。大多数病例为无症状。仔细检查了 99 例病例,包括 4 例恶性和 95 例良性神经鞘瘤。临床分析显示出明显的性别分布(1:1.7,男性对女性)和平均年龄为 58.5 岁。大多数病例为无症状。肿瘤大小从 0.5 厘米到 30 厘米不等,大多数良性病例位于胃,恶性病例位于腹部/小肠。最初的误诊很常见。病理学评估显示出明显的特征,包括良性神经鞘瘤的 Antoni A 和 B 型、梭形细胞和淋巴鞘结构。恶性病例表现出非典型细胞、溃疡和侵袭性生长。免疫组织化学标志物,如 S100、SOX10 和波形蛋白,通过准确诊断显示出一致性的阳性。治疗结果表明恶性病例预后不良,总生存期从 10 个月到 41 个月不等。相比之下,良性病例在随访期间没有复发或转移,尽管存在非典型行为。
本研究强调了腹部神经鞘瘤的罕见性,并强调了全面的诊断形态学和免疫组织化学的必要性。SOX10 是准确诊断的关键且特异性标志物。进一步的研究对于完善诊断方案和增强我们对腹部神经鞘瘤临床行为的理解至关重要。