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伴有局灶性基质形成、酷似骨肉瘤的原发性骨横纹肌肉瘤。

Primary osseous rhabdomyosarcoma with focal matrix formation mimicking osteosarcoma.

作者信息

Kordek Radzislaw, Sowa Piotr, Panasiuk Michal, Kmieciak Marek, Chudobinski Cezary, Pluciennik Elzbieta, Bednarek Andrzej K, Potemski Piotr, Jesionek-Kupnicka Dorota

机构信息

Department of Oncology, Medical University of Lodz, Paderewskiego 4, 93-509, Poland.

出版信息

Pathol Res Pract. 2007;203(12):873-7. doi: 10.1016/j.prp.2007.08.003. Epub 2007 Oct 1.

Abstract

We present an unusual case of primary osseous pleomorphic rhabdomyosarcoma with focal matrix formation mimicking osteosarcoma. The patient was a 21-year-old man who had suffered from pain and slight enlargement of his left calf for 2 months. A plain radiograph demonstrated a large, predominantly osteolytic mass in the region of the proximal fibula with features typical of malignant primary bone tumor. On open surgical biopsy, the tumor consisted of atypical cells, some of them presenting spindle morphology. Between them, there were bands of densely hyalinized matrix with osteoid appearance, but without definite lacunae or calcifications, and an osteosarcoma was diagnosed. Consequently, the tumor was removed. The postoperative tissue presented more pleomorphic cells with some definite rhabdomyoblasts. Desmin, actin, Myf4, and MyoD1 were positive in tumor cells, and a diagnosis of rhabdomyosarcoma was eventually made. Only few cases of primary pure bone rhabdomyosarcoma have been reported. Other bone tumors with rhabdomyosarcomatous differentiation have been described: dedifferentiated chondrosarcoma, fibrosarcoma, and osteosarcoma. Our case does not meet the criteria for sclerosing rhabdomyosarcoma, as matrix formation is focal and cells are spindle-shaped and pleomorphic. However, it is a further example of a diagnostic error in connection with primary osseous tumor.

摘要

我们报告一例罕见的原发性骨多形性横纹肌肉瘤,伴有局灶性基质形成,酷似骨肉瘤。患者为一名21岁男性,左小腿疼痛并轻度肿大2个月。X线平片显示腓骨近端区域有一个大的、以溶骨性为主的肿块,具有原发性恶性骨肿瘤的典型特征。手术切开活检时,肿瘤由非典型细胞组成,其中一些呈梭形形态。其间有呈骨样外观的致密玻璃样变性基质带,但无明确的陷窝或钙化,诊断为骨肉瘤。因此,肿瘤被切除。术后组织显示更多的多形性细胞,并有一些明确的横纹肌母细胞。结蛋白、肌动蛋白、Myf4和MyoD1在肿瘤细胞中呈阳性,最终诊断为横纹肌肉瘤。原发性纯骨横纹肌肉瘤仅报道过少数病例。其他具有横纹肌肉瘤分化的骨肿瘤也有描述:去分化软骨肉瘤、纤维肉瘤和骨肉瘤。我们的病例不符合硬化性横纹肌肉瘤的标准,因为基质形成是局灶性的,细胞呈梭形且多形性。然而,这是原发性骨肿瘤诊断错误的又一个例子。

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