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胸腺瘤:33例临床病理回顾

Thymolipoma: clinicopathologic review of 33 cases.

作者信息

Moran C A, Rosado-de-Christenson M, Suster S

机构信息

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

出版信息

Mod Pathol. 1995 Sep;8(7):741-4.

PMID:8539231
Abstract

The clinical, radiologic, and pathologic features of 33 cases of mediastinal thymolipoma are presented. The patients' ages ranged from 2 to 64 (mean, 33) years; 18 were male and 15 were female. Clinically, the majority of patients (18 cases) were asymptomatic. Five patients presented with upper respiratory symptoms, two patients presented with chest pain, two patients with myasthenia gravis, and one patient with a neck mass; no clinical information was available in four patients. All the tumors were located in the anterior mediastinum and in all cases complete surgical resection of the mass was accomplished. Radiographically, 20 cases showed an anterior mediastinal tumor; when available, computed tomography and/or magnetic resonance imaging demonstrated a mixture of fat and soft tissue elements in these tumors. Grossly, the tumors were described as fairly well-circumscribed, soft, yellowish, fatty tumors with focal solid areas. The tumors varied in size from 4.5 to 36 cm in greatest dimension. Histologically, they were characterized by the presence of abundant mature adipose tissue admixed with areas containing remnants of thymic tissue. The fatty tissue consisted of mature adipocytes devoid of atypia, and the thymic tissue component varied from strands of atrophic thymic epithelium to large areas containing thymic parenchyma showing the typical mixed epithelial/lymphocytic architecture with numerous Hassall's corpuscles. Areas of calcification and cystic degeneration of Hassall's corpuscles were quite prominent in a large number of cases. Our study shows that thymolipomas span the age ranges from the very young to adult individuals with a slight prevalence for patients under the age of 40.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文报告了33例纵隔脂肪纤维瘤的临床、放射学及病理学特征。患者年龄范围为2至64岁(平均33岁);男性18例,女性15例。临床上,大多数患者(18例)无症状。5例患者出现上呼吸道症状,2例患者出现胸痛,2例患者患有重症肌无力,1例患者有颈部肿块;4例患者无临床信息。所有肿瘤均位于前纵隔,所有病例均完成了肿块的完整手术切除。放射学检查显示,20例患者有前纵隔肿瘤;计算机断层扫描和/或磁共振成像显示这些肿瘤中存在脂肪和软组织成分混合。大体上,肿瘤被描述为边界相当清晰、质地柔软、淡黄色的脂肪性肿瘤,伴有局灶性实性区域。肿瘤最大直径为4.5至36厘米不等。组织学上,其特征是存在大量成熟脂肪组织,并混有含胸腺组织残余的区域。脂肪组织由无异型性的成熟脂肪细胞组成,胸腺组织成分从萎缩的胸腺上皮条索到含有胸腺实质的大片区域不等,显示典型的上皮/淋巴细胞混合结构,有大量哈氏小体。大量病例中哈氏小体的钙化和囊性变区域相当明显。我们的研究表明,脂肪纤维瘤患者年龄跨度从幼儿到成人,40岁以下患者略有居多。(摘要截选于250字)

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