Sclerosing Polycystic Adenosis of the Parotid Gland: Report of a Bifocal, Paucicystic Variant with Ductal Carcinoma in situ and Pronounced Stromal Distortion Mimicking Invasive Carcinoma

被引:24
作者
Petersson F. [1 ]
Tan P.H. [2 ]
Hwang J.S.-G. [2 ]
机构
[1] Department of Pathology, National University Health System, Singapore 119074
[2] Department of Pathology, Singapore General Hospital, Singapore
关键词
Carcinoma; Salivary gland; Sclerosing polycystic adenosis;
D O I
10.1007/s12105-011-0242-6
中图分类号
学科分类号
摘要
We present a case (female patient, age 45 years) with a bifocal, paucicystic variant of sclerosing polycystic adenosis of the parotid gland with cribriform ductal carcinoma in situ (DCIS) and pronounced stromal distortion affecting the in situ component to such an extent that it gave a distinct impression of intralesional invasive adenocarcinoma. P63-and calponin-positive myoepithelial cells were present in the periphery of the acini and ducts in the benign component, somewhat discontinuously in the DCIS-component, and even in the periphery of the small irregular atypical cell nests that appeared infiltrative on the haematoxylin and eosin stained sections. Strong cytoplasmic immunoreactivity for GCDFP-15 was detected in the benign component with a variable, patchy and mostly weak positivity in the DCIS. More than 90% of the cells in the DCIS component displayed strong nuclear immunoreactivity for androgen receptors and 10% of the benign ducts showed positivity. Weak to moderate nuclear immunoreactivity for estrogen receptors was seen in 30% of cells in the benign ductal component whereas the DCIS was negative. Occasional cells in the adenosis-component were weakly positive for PR. The proliferative activity (Mib-1/Ki-67) was low (1-2%) in the benign component whereas increased proliferation was seen in the DCIS and in the areas with pseudoinfiltration which also featured atypical mitoses. © 2011 Springer Science+Business Media, LLC.
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页码:188 / 192
页数:4
相关论文
共 16 条
[1]  
Smith B.C., Ellis G.L., Slater L.J., Foss R.D., Sclerosing polycystic adenosis of major salivary glands. A clinicopathologic analysis of nine cases, Am J Surg Pathol, 20, pp. 161-170, (1996)
[2]  
Bharadwaj G., Nawroz I., O'regan B., Sclerosing polycystic adenosis of the parotid gland, Br J Oral Maxillofac Surg, 45, pp. 74-76, (2007)
[3]  
Etit D., Pilch B.Z., Osgood R., Faquin W.C., Fine-needle aspiration biopsy findings in sclerosing polycystic adenosis of the parotid gland, Diagn Cytopathol, 35, pp. 444-447, (2007)
[4]  
Fulciniti F., Losito N.S., Ionna F., Longo F., Aversa C., Botti G., Foschini M.P., Sclerosing polycystic adenosis of the parotid gland: Report of one case diagnosed by fine-needle cytology with in situ malignant transformation, Diagn Cytopathol, 38, pp. 368-373, (2010)
[5]  
Gnepp D.R., Wang L.J., Brandwein-Gensler M., Slootweg P., Gill M., Hille J., Sclerosing polycystic adenosis of the salivary gland: A report of 16 cases, Am J Surg Pathol, 30, pp. 154-164, (2006)
[6]  
Gupta R., Jain R., Singh S., Gupta K., Kudesia M., Sclerosing polycystic adenosis of parotid gland: A cytological diagnostic dilemma, Cytopathology, 20, pp. 130-132, (2009)
[7]  
Gurgel C.A., Freitas V.S., Ramos E.A., Santos J.N., Sclerosing polycystic adenosis of the minor salivary gland: Case report, Braz J Otorhinolaryngol, 76, (2010)
[8]  
Imamura Y., Morishita T., Kawakami M., Tsuda G., Fukuda M., Sclerosing polycystic adenosis of the left parotid gland: Report of a case with fine needle aspiration cytology, Acta Cytol, 48, pp. 569-573, (2004)
[9]  
Meer S., Altini M., Sclerosing polycystic adenosis of the buccal mucosa, Head Neck Pathol, 2, pp. 31-35, (2008)
[10]  
Noonan V.L., Kalmar J.R., Allen C.M., Gallagher G.T., Kabani S., Sclerosing polycystic adenosis of minor salivary glands: Report of three cases and review of the literature, Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 104, pp. 516-520, (2007)