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A Pure Ovarian insular Carcinoid Tumor: A Case Report

Mine Genç, Serap Karaarslan, Berhan Genç, Oya Nermin Sivrikoz, Muhittin Akyıldız, Osman Zekioğlu

Abstract


 Introduction: Carcinoid tumors are rare tumors that are defined as a slow-growing neuroendocrine tumor. They are very rare in ovaries. They can be primarily of ovarian origin or may be found as metastatic lesions in ovaries.

Presentation of Case: A 67-year-old postmenopausal woman presented with vaginal bleeding. Her transvaginal ultrasonography revealed a smooth-contoured solid mass of 8.5x6 cm in right adnexal region. Total abdominal hysterectomy with bilateral salpingo-oophorectomy was performed. Postoperative histopathological examination revealed pure ovarian insular carcinoid tumor. No chemotherapy or radiotherapy was applied. No residual or recurrent pathology was observed during follow-ups for 3 years following the operation.

Conclusion: Carcinoid tumors may rarely be as pure tumors. The histopathological diagnosis is challenging. Surgical therapy is the only option, and chemotherapy and radiotherapy have no role in management of these tumors.


 


Keywords


Ovary; primary carcinoid tumor; pure insular

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References


Zuetenhorst JM, Taal BG. Metastatic carcinoid tumors: a clinical review. Oncologist. 2005, 10:123-31

Talerman A. Germ cell tumor of the ovary. In: Kurman RJ, editor. Blaunstein’s Pathology of The Female Genital Tract. New York’ Springer-Verlag. 2002, 1006-1008

Wong FS, Teo M. An Unusual Case of Presacral Carcinoid Tumor and the Approach of Management. American Journal of Cancer Case Reports. 2013, 1:28-34

Athavale RD, Davies-Humphreys JD, Cruickshank DJ. Primary carcinoid tumours of the ovary. J Obstet Gynaecol. 2004, 24:99-101

Shepherd JH: Revised FIGO staging for gynaecological cancer. Br J Obstet Gynaecol.1989, 96: 889-892

Tavassoli FA, Devilee P World health organization classi-Wcation of tumors. In: Tavassoli FA, Devilee P (eds) Pathology and genetics of tumors of the breast and female genital organs. IARC Press, Lyon. 2003, pp 172-173

Davis KP, Hartmann LK, Keeney GL, Shapiro H. Primary ovarian carcinoid tumors. Gynecol Oncol 1996, 61:259-265

Caruso PA, Marsh MR, Minkowitz S, Karten G. An intense clinicopathologic study of 305 teratomas of theovary. Cancer. 1971,27:343-348

Hajdu SI, Winawer SJ, Myers WP. Carcinoid tumors. A study of 204 cases. Am J Clin Pathol 1974, 61:521-528

Talerman A. Carcinoid tumors of the ovary. J Cancer Res Clin Oncol. 1984, 107:125-135

Talerman A: Germ cell tumors of the ovary. In Blaustein's Pathology of the Female Genital Tract. 5th edition. Edited by Kurman RJ. New York: Springer-Verlag. 2002,967-1033.

Robboy SJ, Norris HJ, Scully RD. Insular carcinoid primary in the ovary: a clinopathologic analysis of 48 cases. Cancer. 1975, 36:404-418

Díaz-Montes TP, Rosenthal LE, Bristow RE, Grumbine FC. Primary insular carcinoid of the ovary. Gynecol Oncol. 2006, 101:175-178

Czernobilsky B, Segal M, Dgani R. Primary ovarian carcinoid with marked heterogeneity of microscopic features. Cancer. 1984;54:585-589

Bai X, Li N, Wang F, Li S, Yu Q. Primary ovarian trabecular carcinoid tumor: a case report and literature review. Arch Gynecol Obstet. 2010, 282:407-411

Roy Somak Mandal Shramana Saroha Vijay•Khurana Nita. Primary carcinoid tumor of the ovary: a case report. Arch Gynecol Obstet. 2008, 277:79-82


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