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胸膜硬纤维瘤:一种局部纤维瘤的临床病理模拟物。

Desmoid tumors of the pleura: a clinicopathologic mimic of localized fibrous tumor.

作者信息

Wilson R W, Gallateau-Salle F, Moran C A

机构信息

Department of Pulmonary and Mediastinal Pathology, Armed Forces Institute of Pathology, Washington, DC, USA.

出版信息

Mod Pathol. 1999 Jan;12(1):9-14.

PMID:9950156
Abstract

Intrathoracic desmoid tumors of the pleura are unusual tumors that are often clinically and histologically confused with localized fibrous tumor of the pleura or benign neurogenic tumors. We studied four cases of intrathoracic desmoid tumor of the pleura and reviewed the clinical, histopathologic, and immunohistochemical features of the four patients. Two men and two women, ranging in age from 16 to 66 years (mean, 44 yr) comprised the study group. Three patients presented with chest pain and one with shortness of breath. Two patients had a history of associated trauma in the area of the tumor. Three of the lesions were based in the parietal pleura and one in the visceral pleura. Treatment included complete resection (two cases), subtotal resection (one case), and subtotal resection followed by radiation therapy and complete resection (one case). The mean tumor size was 12.5 cm, and all of the tumors exhibited a bosselated, firm, white, cut surface. The histologic features of intrathoracic desmoid tumors were similar to those of desmoid tumors at more conventional sites. Infiltration of the adjacent fat and skeletal muscle was invariably present. The tumor cells were immunoreactive for vimentin, desmin, smooth muscle actin, and muscle-specific actin in three of the four cases and were negative for S-100 protein. Follow-up to date shows stable residual disease at 12 months (one case) and two patients with no evidence of disease at 12 and 96 months, respectively. Intrathoracic desmoid tumors often exhibit clinical and radiographic features similar to localized fibrous tumor of the pleura. They generally have histologic and behavioral characteristics identical to those of desmoid tumors at conventional sites. Like desmoid tumors elsewhere, complete resection with negative margins is vital to prevent local recurrence. Desmoid tumor should be considered in the differential of localized fibrous tumor of the pleura.

摘要

胸膜胸内硬纤维瘤是一种罕见的肿瘤,在临床和组织学上常与局限性胸膜纤维瘤或良性神经源性肿瘤相混淆。我们研究了4例胸膜胸内硬纤维瘤,并回顾了这4例患者的临床、组织病理学和免疫组化特征。研究组包括2名男性和2名女性,年龄在16至66岁之间(平均44岁)。3例患者表现为胸痛,1例表现为气短。2例患者在肿瘤部位有相关外伤史。3个病变位于壁层胸膜,1个位于脏层胸膜。治疗方法包括完整切除(2例)、次全切除(1例)以及次全切除后放疗并最终完整切除(1例)。肿瘤平均大小为12.5 cm,所有肿瘤切面均呈分叶状、质地硬、白色。胸内硬纤维瘤的组织学特征与更常见部位的硬纤维瘤相似。总是存在对邻近脂肪和骨骼肌的浸润。4例中有3例肿瘤细胞波形蛋白、结蛋白、平滑肌肌动蛋白和肌特异性肌动蛋白免疫反应阳性,S-100蛋白阴性。截至目前的随访显示,1例患者在12个月时残留疾病稳定,另外2例患者分别在12个月和96个月时无疾病证据。胸内硬纤维瘤通常表现出与局限性胸膜纤维瘤相似的临床和影像学特征。它们一般具有与常见部位硬纤维瘤相同的组织学和行为特征。与其他部位的硬纤维瘤一样,切缘阴性的完整切除对于预防局部复发至关重要。在鉴别局限性胸膜纤维瘤时应考虑硬纤维瘤。

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