You are here

Pineal Bölge Tümörleri

Pineal Region Tumors

Journal Name:

Publication Year:

Keywords (Original Language):

Abstract (2. Language): 
Pineal region tumors cover a large spectrum of benign and malignant tumor structures with multiple cell types. Germ cell tumors are more frequent in men and whereas the frequency of pineal cell tumors is equal in both sexes. Generally, obstructive type hydrocephalus accompanies this situation. As a result of this, increased intracranial pressure symptoms appear. MRI and germ cell markers are diagnostically valuable. Malignant germ cell or pineal cell tumors disseminate through CSF flow circulation into ventricles or spinal cord. The histological diagnosis should be made for the optimal treatment of pineal region tumors, because of the various tumor subtypes. Although current microsurgery techniques provide acceptable mortality and morbidity results, the surgical resection is difficult. The surgical intervention is curative for benign tumors and germ cell tumors and is positively correlated with the lifespan.
Abstract (Original Language): 
Pineal bölge tümörleri; çok çeşitli hücre tiplerinin oluşturduğu benign ve malign tümör yapıları içeren geniş bir spektrumu içerir. Germ hücre tümörleri erkeklerde daha sık görülürken, pineal hücre tümörleri erkek ve kadınlarda eşit oranda görülür. Genellikle obstruktif tip hidrosefali ile birliktelik gösterir ve bu sebeple artmış intrakranial basınç semptomları ile ortaya çıkarlar. Tanıda genel değerlendirme MRG (magnetik rezonans görüntüleme) ve germ hücre belirteçleridir(alfa feto protein ve beta HCG). Malign germ hücreli veya pineal hücreli tümörler BOS akım yollarını izleyerek ventriküllere veya spinal korda yayılabilirler. Tümör subtiplerinin çeşitliliği sebebiyle pineal bölge tümörlerinin optimal klinik tedavisi için histolojik tanı mutlaka gereklidir. Mevcut mikrocerrahi teknikleri ile morbidite ve mortalite sonuçları kabul edilebilir düzeyde ise de cerrahi rezeksiyon güçtür. Cerrahi benign tümörler ve germ hücreli tümörler için genellikle küratiftir ve yaşam süresi ile pozitif korelasyon gösterir.
205-210

REFERENCES

References: 

1. Jeffrey Bruce. Management of Pineal Region Tumors.
Neurosurgery Quarterly 1993;3:103-19.
2. Zulch KJ. Reflectionns o n the surgery of the pineal gland (a
glimse into the past). Neurosurg Rev 1981;4:159-62.
3. Abay EO, Lows ER, Grado GL et al: Pineal Tumors in
Children and adolescents 1981;55:889-95.
4. Cummins FM, Taveras JM, Schlesinger EB. Treatment of
gliomas of the third ventricle and pinealomas. With special
reference to the value of radiotheraphy. Neurology
1960;10:1031-6.
5. Degriolami U, Schimidek H. Clinicopathological study of 53
tumors of the pineal region. J Neurosurg 1973;39:455-62.
6. Joon Ki Kong, Sin Su Jeun, Yong Kil Hong et al. Experience
with pineal region tumors. Child’s Nerv Syst 1998;14:63-68.
7. Chang SM, Hearne PKL, Larson DA, Wara WM, Bollen
AW, Prados MD. Pineoblastoma in adults. Neurosurgery
1995;37:383-391.
8. Jeffery N Bruce, Bennet M Stein, Sander Canndy. Pineal cell
and germ tumors. In: Kaye AH (ed). Brain Tumors. Second
Edition. Churchill Livingstone; 2001.771-803.
9. Stein BM, Bruce J N. Surgical management of pineal region
tumors. Clinical Neurosurgery. Baltimore: Williams and
Wilkins, 1992.
10. Schild SE, Scheithower BW, Schomberg PJ, et al. Pineal
parencimal tumors. Clinical patholojic and therapotic
aspects. Cancer 1993;72:870-880.
11. Turgut Özkaya. Pineal bölge tümörleri: Patolojik özellikleri
ve cerrahi yaklaşım şekilleri. Arşiv 2001;10:100-18.
12. Quest DQ, Kleragia E. Microsurgical anatomy of the pineal
region. Neurosurgery 1980;6:385-90.
13. Yamamoto I, Kageyama N. Microsurgical anatomy of the
pineal region. J Neurosurg 1980;53:205-21.
14. Erlich SS, Apuzzo KLJ. The Pineal Gland:Anatomy,
Physiology and Clinical Significance. J Neurosurg
1985;63:321-41.
15. Jennigs MT, Gelman R, Hochberg F. İntracranial germ cell
tumors:Natural history and pathogenesis. J Neurosurg
1985;63:155-67.
16. Stein BM, Bruce JN. Surgical management of pineal region
tumors. Clin Neurosurg 1992;39:509-32.
17. Rozario R, Adelman L, Prager RJ, Stein BM. Menegiomas of
the pineal regionc and third ventricle. Neurosurgery
1979;5:489-95.
18. Fain JS, Tomlinson FH, Scheithauer BW, Parisi JE, Fletcher
GP, Kelly PJ, Miller GM. Symtomatic glial cysts of the
pineal gland. J Neurosurg 1994;80:454-60.
19. Fetell MR, Bruce JN, Burke AM, et al. Non-neoplsticpineal
cysts. Neurology 1991;41:1034-40.
20. Anderson RCE, Bruce JN. Current management of
germinomas. Contemporary Neurosurgery 2003;25:6.
21. Bruce JN, Stein BM. İnfratentorial approach to pineal
tumors. In: Wilson CB (ed). Neurosurgical purocedures:
Personal approaches to classic operations. Baltimore:
Williams and Wilkins; 1992. 63-76.
22. Allen JC, Nisselbaulh J, Epstein F, Rosen G, Schwartz MK.
Alphafetoprotein and human chorionic gonadotropin
determination in cerebrosipinal fluid. J Neurosurg
1979;51:368-74.
23. Sawaya R, Hawley DK, Tobler WD, Tew JM, Chambers
AA. Pineal and third ventricle tumors. In: Youmans JR (ed).
Neurosurgical Surgery. Philadelphia: WB Saunders; 1990.
3171-203.
24. Korf HW, Bruce JN, Vistica B, Rolag M, Stein BM, Klein
DC. Immunoreactive S-antigen in cerebrospinal fluid a marker of pineal parenchymal tumors. J Neurosurg 1989;70:682-
7.
25. Shinoda J, Yamad H, Sakai, Ando T, Hirata T, Miwa Y.
Placental alkaline phosphatase as a tumor marker for primary
intracranial germinoma. J Neurosurg 1988;68:710-20. F. Abaş, ark.
210
26. Pendl G. Management of pineal region tumors. Neurosurgery
Quarterly 2002;12:279-98.
27. Konovalov AN, Pitskhelauri DI. Principles of treatment of
the pineal region tumors. Surgical Neurol 2003;59:250-68.
28. Bruce JN, Stein BM: Supracerebellar approaches in the
pineal region. In: Apuzzo M (ed): Brain Surgery:
Complication avoidance and management. New York:
Churchill Livingstone; 1993. 511-36.
29. Bruce JN, Stein BM: Supracerebellar approach. In: Kaye A,
Black P (eds): Operative Neurosurgery, Vol. 1. London:
Churchill Livinstone; 2000. 815-24.
30. Dempsey PK, Kondziolka D, Lunsford LD. Stereotactic
diagnosis and treatment of pineal region tumours and
vascular malformationns. Acta Neurochir (Wien) 1992; 116:
14-22.
31. Jean Regis, Pablo Bouillot, Françoise Rouby-Volot,
Dominique Figarella-Branger, Henry Dufour, Jean C
Peragut. Pineal region tumors and the role of stereotactic
biopsy: review of the mortality, morbidity, and diagnosis
rates in 370 cases. Neurosurgery 1996;39:907-24.
32. Edwards MSB, Hudgins RJ, Wilson CB, Levin VA, Wara
WM. Pineal region tumors in children. J Neirosurg
1988;68:689-97.
33. Chang SM, Hearne PKL, Larson DA, Wara WM, Bollen
AW, Prados MD. Pineoblastoma in adults. Neurosurgery
1995;37:383-91.
34. Vaguero J, Ramiro J, Martinez R, Coca S, Bravo G.
Clinicopathological experience with pineocytomas: report of
five surgically terated cases. Neurosurgery 1990;27:612-9.

Thank you for copying data from http://www.arastirmax.com