Targeted molecular profiling of salivary duct carcinoma with rhabdoid features highlights parallels to other apocrine and discohesive neoplasms: which phenotype should drive classification?

Author:

Rooper Lisa M.ORCID,Gagan Jeffrey,Bishop Justin A.

Funder

The Jane B. and Edwin P. Jenevein M.D Endowment for Pathology at UT Southwestern Medical Center

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Otorhinolaryngology,Pathology and Forensic Medicine

Reference59 articles.

1. Kleinsasser O, Klein HJ, Hubner G. [Salivary duct carcinoma. A group of salivary gland tumors analogous to mammary duct carcinoma]. Arch Klin Exp Ohren Nasen Kehlkopfheilkd. 1968;192(1):100–5.

2. Lewis JE, McKinney BC, Weiland LH, Ferreiro JA, Olsen KD. Salivary duct carcinoma. Clinicopathologic and immunohistochemical review of 26 cases. Cancer. 1996;77(2):223–30.

3. Brandwein-Gensler MS, Skalova A, Nagao T. Salivary duct carcinoma. In: Barnes L, Eveson JW, Reichart P, Sidransky D. International Agency for Research on Cancer., editor. Pathology and genetics of head and neck tumours. World Health Organization classification of tumours. Lyon: IARC; 2005. pp. 236–7.

4. Nagao T, Licitra L, Loening T, Vielh P, Williams MD. Salivary duct carcinoma. In: El-Naggar A, Chan JK, Grandis JR, Takata T, Slootweg PJ, editors. WHO Classification of Head and Neck Tumours. Lyon: International Agency for Research on Cancer; 2017. pp. 173–4.

5. Chiosea SI, Williams L, Griffith CC, Thompson LD, Weinreb I, Bauman JE, et al. Molecular characterization of apocrine salivary duct carcinoma. Am J Surg Pathol. 2015;39(6):744–52.

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