Abstract
Primary diseases of the seminal vesicles (SV) are very rare entities.
Nonneoplastic lesions of the seminal vesicles include amyloidosis, inflammation, calcification and calculi, radiation-induced changes, and basal cell proliferation.
Seminal vesicles are frequently involved by tumors originating elsewhere, in particular by prostatic adenocarcinoma, urothelial carcinoma, and rectal adenocarcinoma. On the contrary, primary tumors of the seminal vesicles are rare. Among these, the most common is seminal vesicle adenocarcinoma. To date, less than 100 cases have been reported in literature. Morphologically, primary SV adenocarcinoma is described as a papillary or sheetlike growth architecture, with trabecular and glandular patterns, composed by hobnail tumor cells, frequently with mucinous differentiation. On the contrary, mesenchymal tumors include benign lesions such as leiomyoma, schwannoma, fibroma, paraganglioma, solitary fibrous tumor, cystadenoma, and mixed epithelial and stromal tumors (MEST).
Cystadenoma is a rare benign tumor, while MESTs are biphasic tumors with stromal and benign epithelial components. Histological features such as stromal atypia, mitotic activity, nuclear pleomorphism, and tumor necrosis distinct MEST in low-, intermediate-, and high-grade tumors.
In recent years, multiple studies reported a link between tumorigenesis and tumor microenvironment. In this regard, the molecular mechanisms connecting prostate cancer (PCa) progression and the host microenvironment have been described and include extracellular matrix (ECM), myofibroblasts, cancer-associated fibroblasts (CAFs), neuroendocrine cells, adipose tissue, and the immune-modulatory cells. Of note, only one study evaluated the influence of seminal vesicle’s tumor microenvironment (SVME) on prostate cancer cells so far. Besides, in vivo experiments in NOD/SCID mice clarified the influence of SVME on PCa progression. As such, the injection of PC3 cells into the prostate or the SV resulted in different tumor aggressiveness, and the incidence of retroperitoneal lymph node metastases was significantly higher in mice models receiving SV injection. These findings demonstrated that SVs (rather than the prostate) offer a stimulating tumor microenvironment for growth and invasion of prostate cancer cells.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Aumüller G, Riva A (1992) Morphology and functions of the human seminal vesicle. Andrologia 24(4):183–196
Kuo T, Gomez LG (1981) Monstrous epithelial cells in human epididymis and seminal vesicles. A pseudomalignant change. Am J Surg Pathol 5(5):483–490
Shidham VB, Lindholm PF, Kajdacsy-Balla A, Basir Z, George V, Garcia FU (1999) Prostate-specific antigen expression and lipochrome pigment granules in the differential diagnosis of prostatic adenocarcinoma versus seminal vesicle-ejaculatory duct epithelium. Arch Pathol Lab Med 123(11):1093–1097
Clavert A, Cranz C, Bollack C (1990) Functions of the seminal vesicle. Andrologia 22(Suppl 1):185–192
Argon A, Sımşır A, Sarsik B, Tuna B, Yörükoğlu K, Nıflıoğlu GG, Sen S (2012) Amyloidosis of seminal vesicles; incidence and pathologic characteristics. Turk Patoloji Derg 28(1):44–48. https://doi.org/10.5146/tjpath.2012.01096
Pitkänen P, Westermark P, Cornwell GG 3rd, Murdoch W (1983) Amyloid of the seminal vesicles. A distinctive and common localized form of senile amyloidosis. Am J Pathol 110(1):64–69
Irwin WK (1936) The ætiology and treatment of prostatitis and Vesiculitis. Br J Vener Dis 12(1):29–34. https://doi.org/10.1136/sti.12.1.29
Zaidi S, Gandhi J, Seyam O, Joshi G, Waltzer WC, Smith NL, Khan SA (2019) Etiology, diagnosis, and management of seminal vesicle stones. Curr Urol 12(3):113–120. https://doi.org/10.1159/000489429
Montironi R, Lopez-Beltran A, Cheng L, Galosi AB, Montorsi F, Scarpelli M (2014) Seminal vesicle intraepithelial neoplasia versus basal cell hyperplasia in a seminal vesicle. Eur Urol 66(4):623–627. https://doi.org/10.1016/j.eururo.2014.02.054
Campobasso D, Fornia S, Ferretti S et al (2012) Primary bilateral seminal vesicle carcinoma: description of a case and literature review. Int J Surg Pathol 20:633–635
Ormsby AH, Haskell R, Jones D et al (2000) Primary seminal vesicle carcinoma: a immunohistochemical analysis of four cases. Mod Pathol 13:46–51
Zhu H, Gan H, Shi Z, Pei Y, Sun B (2018) Experience of treating a young patient with primary seminal vesicle adenocarcinoma. Clin Genitourin Cancer 16(3):e547–e552. https://doi.org/10.1016/j.clgc.2018.02.008
Terrisse S, Comblor ME, VĂ©rine J, Gauthier H, Mongiat-Artus P, Culine S (2017) Primary adenocarcinoma of the seminal vesicle. Rare Tumors 9(3):7074. https://doi.org/10.4081/rt.2017.7074
Katafigiotis I, Mitsos P, Kousournas G et al (2017) Primary adenocarcinoma of the seminal vesicles: a very rare neoplasia occurring in a 56-year-old patient. Clin Genitourin Cancer 15(1):e127–e129. https://doi.org/10.1016/j.clgc.2016.06.015
Lal H, Yadav P, Jena R, Jain M (2017) Metastatic primary seminal vesicle adenocarcinoma: management of a rare tumour with multiagent chemotherapy and hormonal therapy. BMJ Case Rep. pii: bcr-2017-221896. https://doi.org/10.1136/bcr-2017-221896
Thyavihally YB, Tongaonkar HB, Gupta S et al (2007) Primary seminal vesicle adenocarcinoma presenting as isolated metastasis to penis responding to chemotherapy and hormonal therapy. Urology 69:778e1–778e3
Yin T, Jiang Y (2108) A 5-year follow-up of primary seminal vesicle adenocarcinoma: a case report. Medicine (Baltimore) 97(41):e12600
Baschinsky DY, Niemann TH, Maximo CB, Bahnson RR (1998) Seminal vesicle cystadenoma: a case report and literature review. Urology 51:840–845
Santos LD, Wong CS, Killingsworth M (2001) Cystadenoma of the seminal vesicle: report of a case with ultrastructural findings. Pathology 33:399–402
Campi R, Serni S, Raspollini MR, Tuccio A, Siena G, Carini M, Minervini A (2015) Robot-assisted laparoscopic vesiculectomy for large seminal vesicle cystadenoma: a case report and review of the literature. Clin Genitourin Cancer 13(5):e369–e373. https://doi.org/10.1016/j.clgc.2015.02.011
Reikie BA, Yilmaz A, Medlicott S, Trpkov K (2015) Mixed epithelial-stromal tumor (MEST) of seminal vesicle: a proposal for unified nomenclature. Adv Anat Pathol 22(2):113–120. https://doi.org/10.1097/PAP.0000000000000057
Ohori M, Scardino PT, Lapin SL, Seale-Hawkins C, Link J, Wheeler TM (1993) The mechanisms and prognostic significance of seminal vesicle involvement by prostate cancer. Am J Surg Pathol 17(12):1252–1261. https://doi.org/10.1097/00000478-199312000-00006
Edge S, Byrd DR, Compton CC, Fritz AG, Greene FL, Trotti A AJCC cancer staging manual, 7th edn. Springer, New York. https://doi.org/10.1007/978-1-4757-3656-4
D’Amico AV, Whittington R, Malkowicz SB et al (1995) A multivariate analysis of clinical and pathological factors that predict for prostate specific antigen failure after radical prostatectomy for prostate cancer. J Urol 154(1):131–138. https://doi.org/10.1016/S0022-5347(01)67248-3
Epstein JI, Partin AW, Sauvageot J, Walsh PC (1996) Prediction of progression following radical prostatectomy: a multivariate analysis of 721 men with long-term follow-up. Am J Surg Pathol 20(3):286–292. https://doi.org/10.1097/00000478-199603000-00004
Epstein JI, Partin AW, Potter SR, Walsh PC (2000) Adenocarcinoma of the prostate invading the seminal vesicle: prognostic stratification based on pathologic parameters. Urology 56(2):283–288
Kristiansen A, Wiklund F, Wiklund P, Egevad L (2013) Prognostic significance of patterns of seminal vesicle invasion in prostate cancer. Histopathology 62(7):1049–1056. https://doi.org/10.1111/his.12104
Ro JY, Ayala AG, el-Naggar A, Wishnow KI (1987) Seminal vesicle involvement by in situ and invasive transitional cell carcinoma of the bladder. Am J Surg Pathol 11(12):951–958
Amin M (2018) AJCC cancer staging handbook, 8th edn. Springer, New York
Adachi Y, Rokujyo M, Kojima H, Nagashima K (1991) Primary seminoma of the seminal vesicle: report of a case. J Urol 146(3):857–859
Matsuzaki K, Yasunaga Y, Fukuda S, Oka T (2009) Seminal vesicle metastasis of renal cell carcinoma. Urology 74(5):1017–1018. https://doi.org/10.1016/j.urology.2009.04.058
Shen Y, Nie L, Yao Y, Yuan L, Liu Z, Lv Y (2019) Seminal vesicle metastasis after liver transplantation for hepatocellular carcinoma: a case report. Medicine (Baltimore) 98(3):e13770. https://doi.org/10.1097/MD.0000000000013770
Wang M, Zhao J, Zhang L et al (2017) Role of tumor microenvironment in tumorigenesis. J Cancer 8(5):761–773. https://doi.org/10.7150/jca.17648
Fidler IJ (1990) Critical factors in the biology human cancer metastasis: twenty-eighth G. G. A. Clowes memorial award lecture. Cancer Res 50:6130–6138
Alencar H, King R, Funovics M, Stout C, Weissleder R, Mahmood U (2005) A novel mouse model for segmental orthotopic colon cancer. Int J Cancer 117:335–339
Sato N, Gleave ME, Bruchovsky N, Rennie PS, Beraldi E, Sullivan LD (1997) A metastatic and androgen-sensitive human prostate cancer model using intraprostatic inoculation of LNCaP cells in SCID mice. Cancer Res 57:1584–1589
Gohji K, Nakajima M, Boyd D, Dinney CP, Bucana CD, Kitazana S, Kamidono S, Fidler IJ (1997) Organ-site dependence for the production of urokinase-type plasminogen activator and metastasis by human renal cell carcinoma cells. Am J Pathol 151:1655–1661
Shi J, Wang L, Zou C et al (2018) Tumor microenvironment promotes prostate cancer cell dissemination via the Akt/mTOR pathway. Oncotarget 9(10):9206–9218. https://doi.org/10.18632/oncotarget.24104
Ganguly SS, Li X, Miranti CK (2014) The host microenvironment influences prostate cancer invasion, systemic spread, bone colonization, and osteoblastic metastasis. Front Oncol 4:364. https://doi.org/10.3389/fonc.2014.00364
Chen F, Zhuang X, Lin L, Yu P, Wang Y, Shi Y, Hu G, Sun Y (2015) New horizons in tumor microenvironment biology: challenges and opportunities. BMC Med 13:45
Kumano M, Miyake H, Kurahashi T, Yamanaka K, Fujisawa M (2008) Enhanced progression of human prostate cancer PC3 cells induced by the microenvironment of the seminal vesicle. Br J Cancer 98(2):356–362. https://doi.org/10.1038/sj.bjc.6604169
Festuccia C, Dolo V, Guerra F, Violini S, Muzi P, Pavan A, Bologna M (1998) Plasminogen activator system modulated invasive capacity and proliferation in prostatic tumor cells. Clin Exp Metastasis 16:513–528
Unlu A, Leake RE (2003) Transforming growth factor b1 stimulates urokinase plasminogen activator system on prostate cancer cells. Int J Biol Markers 18:147–151
Choong PF, Nadesapillai AP (2003) Urokinase plasminogen activator system: a multifunctional role in tumor progression and metastasis. Clin Orthop Relat Res 415:S46–S58
Prazeres PHDM, Leonel C, Silva WN et al (2020) Ablation of sensory nerves favours melanoma progression. J Cell Mol Med
Birbrair A, Zhang T, Wang ZM, Messi ML, Mintz A, Delbono O (2015) Pericytes at the intersection between tissue regeneration and pathology. Clin Sci (Lond) 128(2):81–93. https://doi.org/10.1042/CS20140278
Birbrair A, Zhang T, Wang ZM, Messi ML, Olson JD, Mintz A, Delbono O (2014) Type-2 pericytes participate in normal and tumoral angiogenesis. Am J Physiol Cell Physiol 307(1):C25–C38. https://doi.org/10.1152/ajpcell.00084.2014
Ozerdem U (2006) Targeting of pericytes diminishes neovascularization and lymphangiogenesis in prostate cancer. Prostate 66(3):294–304
Welén K, Jennbacken K, Tesan T, Damber JE (2009) Pericyte coverage decreases invasion of tumour cells into blood vessels in prostate cancer xenografts. Prostate Cancer Prostatic Dis 12(1):41–46. https://doi.org/10.1038/pcan.2008.33
Enzinger FM, Smith BH (1976) Hemangiopericytoma. An analysis of 106 cases. Hum Pathol 7:61–82
Hsieh TY, ChangChien YC, Chen WH et al (2011) De novo malignant solitary fibrous tumor of the kidney. Diagn Pathol 6:96–100
Zhao G, Li G, Han R (2012) Two malignant solitary fibrous tumors in one kidney: case report and review of the literature. Oncol Lett 4:993–995
Arya M, Hayne D, Brown RSD et al (2001) Hemangiopericytoma of the seminal vesicle presenting with hypoglycemia. J Urol 166:992
Busato W, Almeida GL, Ogata D (2015) Hemangiopericytoma of seminal vesicle presenting with hypoglycemia. Rev Brasil Oncol ClĂn 11:40
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG
About this chapter
Cite this chapter
Cimadamore, A., Montironi, R., Serni, S., Campi, R. (2020). Seminal Vesicle Tumor Microenvironment. In: Birbrair, A. (eds) Tumor Microenvironments in Organs. Advances in Experimental Medicine and Biology, vol 1296. Springer, Cham. https://doi.org/10.1007/978-3-030-59038-3_19
Download citation
DOI: https://doi.org/10.1007/978-3-030-59038-3_19
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-59037-6
Online ISBN: 978-3-030-59038-3
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)