13岁女童软骨黏液样纤维瘤样骨肉瘤一例新报告。

IF 1.9 Q3 PATHOLOGY
Clinical Pathology Pub Date : 2021-11-18 eCollection Date: 2021-01-01 DOI:10.1177/2632010X211057555
Sabrine Derqaoui, Oussama Marbouh, Tarik Madhi, Lamalmi Najat, Lamia Rouas
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引用次数: 1

摘要

骨肉瘤(Osteosarcoma, OS)是最常见的原发性非造血骨恶性肿瘤,具有严格的组织学定义:肿瘤细胞产生明确的类骨。罕见的变异显示低级别的组织学特征已被描述;其中软骨粘液样纤维瘤(CMF-OS)最为罕见。然而,尽管其形态平淡无奇;cmf样OS具有侵袭性临床行为和不良预后。据我们所知,只有3例CMF-OS在儿童中被报道过。因为它的非典型性和稀缺性;误诊更容易发生。在这里,我们描述了一个新的病例CMF-OS在一个13岁的女孩致命的结果。诊断基于局灶性恶性骨形成和影像学检查的相关性。本病例介绍的目的是提高对这种罕见实体的认识,并强调具有挑战性的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chondromyxoid Fibroma-Like Osteosarcoma in a 13 Years Old Girl: A Report of a New Case.

Chondromyxoid Fibroma-Like Osteosarcoma in a 13 Years Old Girl: A Report of a New Case.

Chondromyxoid Fibroma-Like Osteosarcoma in a 13 Years Old Girl: A Report of a New Case.

Chondromyxoid Fibroma-Like Osteosarcoma in a 13 Years Old Girl: A Report of a New Case.

Osteosarcoma (OS) is the most common primary non hematopoietic malignant tumor of bone with a strict histologic definition: the presence of unequivocal osteoid produced by neoplastic cells. Rare variants displaying low-grade histological features have been described; among which chondromyxoid fibroma-like (CMF-OS) is the rarest. However, despite its bland morphology; CMF-like OS has an aggressive clinical behavior and a poor prognosis. To the best of our knowledge, only 3 cases of CMF-OS have been previously reported in children. Because of its atypicality and scarcity; misdiagnosis is more likely to occur. Herein we describe a new case of CMF-OS in a 13 years old girl with fatal outcome. Diagnosis was based on focal malignant bone formation and correlation with imaging studies. The aim of the present case presentation is to raise awareness of this rare entity and to highlight the challenging diagnosis.

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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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