National Health Laboratory Service, 121470Stellenbosch University, Cape Town, South Africa.
26697Division of Orthopaedic Surgery, Stellenbosch University, Cape Town, South Africa.
Int J Surg Pathol. 2021 Oct;29(7):798-803. doi: 10.1177/10668969211001449. Epub 2021 Mar 11.
Adamantinoma-like Ewing sarcoma is a rare variant of Ewing sarcoma with histologic and immunohistochemical evidence of squamous differentiation. This variant most commonly occurs in the head and neck region with a few cases reported in the long bones of the limbs. It may be associated with poorer clinical outcome and could pose a diagnostic challenge, particularly if it occurs in older patients or as a metastatic lesion. We present a case of Ewing sarcoma in the metatarsal of an 11-year-old boy that manifested adamantinoma-like morphology after neoadjuvant chemotherapy. Chemotherapy has been reported to induce neuronal maturation and rhabdoid morphology in cases of Ewing sarcoma, but no reports of treatment-induced squamous differentiation with P40/P63 expression have been demonstrated. This is also the first documented case treated with a pedicled osteocutaneous fibular transfer in a metatarsal malignancy, which is usually treated by either ray or below-knee amputation.
类似于造釉细胞瘤的尤文肉瘤是尤文肉瘤的一种罕见变异型,具有鳞状分化的组织学和免疫组织化学证据。这种变体最常见于头颈部,少数病例见于四肢的长骨。它可能与更差的临床结果有关,并可能构成诊断挑战,特别是如果它发生在老年患者或转移性病变中。我们报告了一例发生在 11 岁男孩跖骨的尤文肉瘤,在新辅助化疗后表现出类似于造釉细胞瘤的形态。据报道,化疗可诱导尤文肉瘤中神经元成熟和横纹肌样形态,但尚无报道表明治疗诱导的鳞状分化伴有 P40/P63 表达。这也是首例经 pedicled osteocutaneous fibular transfer 治疗跖骨恶性肿瘤的病例,通常采用射线或膝下截肢治疗。