Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia; Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia; Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia; Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia; NSW Health Pathology, Sydney, NSW, Australia.
Pathology. 2021 Dec;53(7):830-835. doi: 10.1016/j.pathol.2021.02.012. Epub 2021 Jun 2.
Melanoma can present with osteocartilaginous differentiation, however few reports exist on this rare subtype. We present eight cases of melanoma with osteocartilaginous differentiation to highlight its clinical, pathological and molecular features. The cases showed no association with gender (5 males and 3 females) or age (range 23-84 years). Cases included both primary melanomas and distant metastases (6 and 2, respectively), with the majority arising from cutaneous sites (7/8) and the remaining case from a mucosal site. Tumour-infiltrating lymphocyte (TIL) score ranged from 0 to 3 (median 1), and 2/8 lesions had evidence of inflammatory changes or antecedent trauma. No recurrent mutations were found in the tumours by next generation sequencing, and the mutations observed were typical of melanoma rather than osteosarcomatous lesions. The majority of tumours stained positive for melanoma markers including S100, HMB45, Melan-A, SOX10 and MITF. Staining of the osteoblastic marker SATB2 varied from negative to widespread positive. We demonstrate that melanomas with osteocartilaginous differentiation are heterogeneous in presentation and are not typified by a recurrent mutation in cancer associated genes. Where uncertainty exists in diagnosing an osteocartilaginous lesion, a diagnosis of melanoma can be supported by the presence of genomic mutations typical of melanoma such as BRAF, NRAS and NF1, and IHC staining positive for S100, HMB45, Melan-A, SOX10 and MITF. SATB2 may be positive in these lesions and thus should not be used to rule out melanoma.
黑色素瘤可表现出骨软骨分化,然而,关于这种罕见亚型的报道很少。我们报告了 8 例具有骨软骨分化的黑色素瘤病例,以突出其临床、病理和分子特征。这些病例与性别(5 名男性和 3 名女性)或年龄(23-84 岁)无关。病例包括原发性黑色素瘤和远处转移(分别为 6 例和 2 例),大多数起源于皮肤部位(7/8),其余 1 例起源于黏膜部位。肿瘤浸润淋巴细胞(TIL)评分范围为 0-3(中位数为 1),2/8 例病变有炎症变化或先前创伤的证据。下一代测序未发现肿瘤中有复发突变,观察到的突变与黑色素瘤而非骨肉瘤病变典型。大多数肿瘤对黑色素瘤标志物包括 S100、HMB45、Melan-A、SOX10 和 MITF 呈阳性染色。成骨细胞标志物 SATB2 的染色从阴性到广泛阳性不等。我们证明,具有骨软骨分化的黑色素瘤在表现上是异质性的,其特征不是癌症相关基因中反复出现的突变。在诊断骨软骨病变存在不确定性时,如果存在典型的黑色素瘤基因组突变,如 BRAF、NRAS 和 NF1,以及 IHC 染色阳性的 S100、HMB45、Melan-A、SOX10 和 MITF,则支持黑色素瘤的诊断。这些病变中 SATB2 可能为阳性,因此不应将其用于排除黑色素瘤。