Biphenotypic sinonasal sarcoma: A series of six cases with evaluation of role of β-catenin immunohistochemistry iii differential diagnosis
Biphenotypic sinonasal sarcoma: A series of six cases with evaluation of role of β-catenin immunohistochemistry iii differential diagnosis
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DOI:
10.1016/j.anndiagpath.2017.11.005
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发表时间:
2018-04-01
影响因子:
2
通讯作者:
Sharm, Suresh C.
中科院分区:
文献类型:
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作者:
Kakkar, Aanchal;Rajeshwari, Madhu;Sharm, Suresh C.
Introduction: Biphenotypic sinonasal sarcoma (BSNS) is a recently described mesenchymal tumor exclusive to the sinonasal region. It is a low grade sarcoma, displaying evidence of myogenic and neural differentiation. Role of beta-catenin immunohistochemistry in distinguishing it from its morphological mimics is not well-established. We conducted this study to identify cases of BSNS from our archives, and to examine immunopositivity for beta-catenin in them as well as in its close differential diagnosis.Methods: All cases of nasal cavity and paranasal sinus mesenchymal neoplasms were identified. Histopathological features were reviewed. Cases showing smooth muscle actin (SMA) and S-100 immunopositivity, and typical morphology were reclassified as BSNS. beta-catenin immunoexpression was assessed.Results: Twenty-one mesenchymal tumors, including 12 sinonasal hemangiopericytoma (SNHPC), five solitary fibrous tumors (SFT), three BSNS, and one synovial sarcoma were identified. Three SNHPC cases were reclassified as BSNS. BSNS patients included one male and five females, with mean age of 51 years. Five BSNS cases (83.3%) showed nuclear beta-catenin immunopositivity. SNHPC cases also were beta-catenin positive (60%).Conclusion: BSNS is a rare sinonasal neoplasm, frequently misdiagnosed as SNHPC and SFT. beta-catenin immunopositivity is seen in majority of cases, indicating a role in pathogenesis. However, due to positivity in other tumors like SNHPC, it has limited role in differential diagnosis.