Kamal Achmad Fauzi, Anshori Fahmi, Kodrat Evelina
Department of Orthopaedic & Traumatology, Cipto Mangunkusumo National Central Hospital and Faculty of Medicine, Universitas Indonesia, Jalan Diponegoro No. 71, Jakarta Pusat, Jakarta 10430, Indonesia.
Musculoskletal Pathology Division, Departement of Anatomic Pathology, Faculty of Medicine Universitas Indonesia-Cipto Mangunkusumo Hospital, Jakarta, Indonesia.
Int J Surg Case Rep. 2021 Mar;80:105599. doi: 10.1016/j.ijscr.2021.01.093. Epub 2021 Jan 28.
Osteofibrous dysplasia (OFD) and Osteofibrous dysplasia-like Adamantinoma have a similar appearance both in clinical and radiography, but different in its histopathology. Despite this similarity, the treatment and prognosis are different, therefore the diagnosis should be established precisely.
A three-year-old boy was admitted to hospital after falling on his lower leg. A bead size lump appeared on his tibia with pain and swelling, which later became enlarged. Diagnosis of osteofibrous dysplasia and adamantinoma was considered. We performed limb-salvage procedure by curretage, bone grafting, and internal fixation application. The histology section showed woven bone rimmed by polygonal osteoblast cell with intervening fibrous stroma and small nests of tumour cells raised the possibility of epithelial differentiation. The positivity for cytokeratin immunostaining confirmed the diagnosis as osteofibrous dysplasia-like adamantinoma. In this case it is a very rare spectrum of malignancy in children.
These two tumor entities have identical radiographic characteristics, histopathology features the distinction between classic adamantinoma and OFD-like adamantinoma based on the predominant epithelial component. The relationship of osteofibrous dysplasia with adamantinoma is unclear. Several authors considered possible calling relationship osteofibrous dysplasia as "juvenile adamantinoma". However, does not rule out the possible existence of de novo osteofibrous dysplasia not related to adamantinoma.
OFD-like adamantinoma and Osteofibrous Dysplasia had similar histopathology pattern, a pathologist must be aware of this feature and perform immunohistochemical staining for keratin particularly when the histopathological feature of osteofibrous dysplasia showed small nests of tumor cells within the fibrous stroma. diagnostic challenging and require multidisciplinary approach.
骨纤维结构不良(OFD)和骨纤维结构不良样釉质瘤在临床和影像学表现上相似,但组织病理学不同。尽管有这种相似性,但治疗和预后不同,因此应准确做出诊断。
一名三岁男孩小腿受伤后入院。其胫骨上出现珠子大小的肿块,伴有疼痛和肿胀,后来肿块增大。考虑诊断为骨纤维结构不良和釉质瘤。我们通过刮除、骨移植和内固定应用进行了保肢手术。组织学切片显示编织骨被多边形成骨细胞包绕,其间有纤维基质,小巢状肿瘤细胞提示上皮分化的可能性。细胞角蛋白免疫染色阳性证实诊断为骨纤维结构不良样釉质瘤。在这种情况下,它是儿童中一种非常罕见的恶性肿瘤类型。
这两种肿瘤实体具有相同的影像学特征,组织病理学特征基于主要上皮成分区分经典釉质瘤和骨纤维结构不良样釉质瘤。骨纤维结构不良与釉质瘤的关系尚不清楚。几位作者认为骨纤维结构不良可能被称为“青少年釉质瘤”。然而,不排除存在与釉质瘤无关的原发性骨纤维结构不良的可能性。
骨纤维结构不良样釉质瘤和骨纤维结构不良具有相似的组织病理学模式,病理学家必须了解这一特征,并进行角蛋白免疫组织化学染色,特别是当骨纤维结构不良的组织病理学特征显示纤维基质内有小巢状肿瘤细胞时。诊断具有挑战性,需要多学科方法。