Derqaoui Sabrine, Marbouh Oussama, Madhi Tarik, Najat Lamalmi, Rouas Lamia
Department of Pathology, Maternity and Children's Hospital Ibn Sina University Hospital, Rabat, Morocco.
Faculty of Medicine and Pharmacy of Rabat, Mohamed V University of Rabat, Rabat, Morocco.
Clin Pathol. 2021 Nov 18;14:2632010X211057555. doi: 10.1177/2632010X211057555. eCollection 2021 Jan-Dec.
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.
骨肉瘤(OS)是最常见的原发性非造血性骨恶性肿瘤,具有严格的组织学定义:肿瘤细胞产生明确的骨样组织。已经描述了表现出低级别组织学特征的罕见变体;其中软骨黏液样纤维瘤样骨肉瘤(CMF-OS)最为罕见。然而,尽管其形态温和,但CMF样骨肉瘤具有侵袭性的临床行为和较差的预后。据我们所知,此前仅报道过3例儿童CMF-OS病例。由于其非典型性和罕见性,更容易发生误诊。在此,我们描述了一名13岁女孩发生CMF-OS的新病例,该病例导致了致命后果。诊断基于局灶性恶性骨形成并与影像学研究相关联。本病例报告的目的是提高对这种罕见实体的认识,并强调其具有挑战性的诊断。