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1.
Am J Surg Pathol ; 47(11): 1243-1251, 2023 11 01.
Artigo em Inglês | MEDLINE | ID: mdl-37494548

RESUMO

Adamantinoma-like Ewing sarcoma (ALES) is a rare malignancy currently considered a variant of Ewing sarcoma with most known cases harboring EWSR1 rearrangements. Herein we present a series of 6 cases of EWSR1 -negative ALES. The tumors arose in the sinonasal tract (n=3), major salivary glands (submandibular gland=1; parotid=1), and anterior mediastinum (n=1) in patients ranging from 25 to 79 years of age. Most tumors were basaloid in appearance, growing in large nests separated by interlobular fibrosis without overt squamous pearls. However, 1 case closely resembled a well-differentiated neuroendocrine tumor with uniformly round nuclei, eosinophilic cytoplasm, and trabecular architecture. All cases were diffusely positive for pan-cytokeratin, p40 or p63, and CD99. A subset of cases showed diffuse reactivity for synaptophysin, including 1 sinonasal tumor which also demonstrated sustentacular S100 protein expression. Molecular testing showed FUS rearrangements in all cases. Gene partners included known ETS family members FEV (n=2) and FLI1 (n=1). Our results expand the molecular diagnostic considerations for ALES to include FUS rearrangements. We also show that ALES may harbor FUS :: FLI1 fusion, which has not been previously reported in the Ewing family of tumors. Furthermore, ALES may show unusual histologic and immunophenotypic features that can overlap with olfactory carcinoma including S100-positive sustentacular cells. ALES should be considered in the diagnostic differential of small round cell tumors and tumors with neuroendocrine differentiation with immunohistochemical workup to include p40 and CD99/NKX2.2.


Assuntos
Adamantinoma , Tumores Neuroectodérmicos Primitivos Periféricos , Sarcoma de Ewing , Sarcoma , Humanos , Sarcoma de Ewing/diagnóstico , Sarcoma de Ewing/genética , Sarcoma de Ewing/patologia , Adamantinoma/genética , Adamantinoma/patologia , Proteína EWS de Ligação a RNA/genética , Sarcoma/genética , Biomarcadores Tumorais/genética , Proteínas de Fusão Oncogênica/genética , Proteína FUS de Ligação a RNA
2.
Ann Thorac Surg ; 107(5): e349-e351, 2019 May.
Artigo em Inglês | MEDLINE | ID: mdl-30365962

RESUMO

Posterior mediastinal masses centered on the thoracic inlet require a thoughtful operative approach. Herein, a case of a young woman with a symptomatic posterior cervicomediastinal ganglioneuroma is reported to highlight such considerations.


Assuntos
Ganglioneuroma/diagnóstico , Ganglioneuroma/cirurgia , Neoplasias de Cabeça e Pescoço/diagnóstico , Neoplasias de Cabeça e Pescoço/cirurgia , Neoplasias do Mediastino/diagnóstico , Neoplasias do Mediastino/cirurgia , Adulto , Feminino , Humanos
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