J Korean Neurosurg Soc.  2015 Jun;57(6):465-468. 10.3340/jkns.2015.57.6.465.

Sporadic Hemangioblastoma in the Pituitary Stalk: A Case Report and Review of the Literature

Affiliations
  • 1Department of Neurosurgery, Hanyang University Guri Hospital, Guri, Korea. kjm2323@hanyang.ac.kr

Abstract

Hemangioblastomas in the pituitary stalk are especially rare. Most pituitary stalk hemangioblastomas reported in the literature were associated with von Hippel-Lindau (VHL) disease. Here, we report only the 3rd case of sporadic pituitary stalk hemangioblastoma diagnosed in a 60-year-old woman. Despite the danger of potential complications due to excessive vascularity or proximity to important neural structures, the tumor in our case was successfully removed while preserving pituitary function. In this case, complete surgical excision was shown to be an effective treatment option for symptomatic pituitary stalk hemangioblastoma, and we suggest careful evaluation of any highly enhancing mass with a signal void in the pituitary stalk preoperatively, even if no VHL disease is evident.

Keyword

Hemangioblastoma; Pituitary stalk; Suprasellar tumor

MeSH Terms

Female
Hemangioblastoma*
Humans
Middle Aged
Pituitary Gland*

Figure

  • Fig. 1 Preoperative sagittal T1-weighted magnetic resonance image without contrast enhancement reveals an isointense suprasellar mass 10 to 12 mm in dimension located on the pituitary stalk (A). Preoperative sagittal and coronal magnetic resonance images with contrast show strongly enhanced mass involving the pituitary stalk (white arrow) with multiple signal voids inside (black arrows) (B and C).

  • Fig. 2 Intraoperative photograph shows a hyperemic, round mass with a thin capsule (white arrow) (A). The paper thin leafs of the pituitary stalk (asterisk) is revealed after total removal of tumor mass (B).

  • Fig. 3 Photomicrographic view of the tumor specimens showing a vascular lesion composed of prominent thin-walled vessels with vacuolated stromal cells (Hematoxylin and eosin, ×50) (A). Blue circles indicate positively stained endothelial cells (Immunostain for CD34 stain, ×200) (B).

  • Fig. 4 The sagittal (A) and coronal (B) brain magnetic resonance images with contrast which obtained 6 months after complete removal of the tumor demonstrate an intact pituitary stalk and no residual tumor.


Cited by  1 articles

A Case of Sporadic Suprasellar Hemangioblastoma Mimicking Meningioma
Byung-moo Kang, Sang Min Youn
Brain Tumor Res Treat. 2019;7(2):147-150.    doi: 10.14791/btrt.2019.7.e40.


Reference

1. Bachmann K, Markwalder R, Seiler RW. Supratentorial haemangioblastoma. Case report. Acta Neurochir (Wien). 1978; 44:173–177. PMID: 570343.
2. Cao Y, Gao P, Wang S, Zhao J. Pituitary infundibulum hemangioblastoma detected by dynamic enhancement MRI. Can J Neurol Sci. 2010; 37:697–699. PMID: 21059523.
Article
3. Chandler HC Jr, Friedman WA. Radiosurgical treatment of a hemangioblastoma : case report. Neurosurgery. 1994; 34:353–355. discussion 355PMID: 8177399.
4. Ding XH, Zhou LF, Tan YZ, Zhao Y, Zhu JJ. Histologic and histogenetic investigations of intracranial hemangioblastomas. Surg Neurol. 2007; 67:239–245. discussion 245PMID: 17320626.
Article
5. Fomekong E, Hernalsteen D, Godfraind C, D'Haens J, Raftopoulos C. Pituitary stalk hemangioblastoma : the fourth case report and review of the literature. Clin Neurol Neurosurg. 2007; 109:292–298. PMID: 17187928.
Article
6. Goto T, Nishi T, Kunitoku N, Yamamoto K, Kitamura I, Takeshima H, et al. Suprasellar hemangioblastoma in a patient with von Hippel-Lindau disease confirmed by germline mutation study : case report and review of the literature. Surg Neurol. 2001; 56:22–26. PMID: 11546565.
Article
7. Grisoli F, Gambarelli D, Raybaud C, Guibout M, Leclercq T. Suprasellar hemangioblastoma. Surg Neurol. 1984; 22:257–262. PMID: 6540482.
Article
8. Hoff JT, Ray BS. Cerebral hemangioblastoma occurring in a patient with von Hippel-Lindau disease. Case report. J Neurosurg. 1968; 28:365–368. PMID: 5643929.
Article
9. Lee KM, Kim EJ, Choi WS, Kim TS. Pituitary stalk hemangioblastoma in a von Hippel-Lindau patient : clinical course follow-up over a 20-year period. J Korean Neurosurg Soc. 2013; 53:297–299. PMID: 23908704.
Article
10. Lonser RR, Butman JA, Kiringoda R, Song D, Oldfield EH. Pituitary stalk hemangioblastomas in von Hippel-Lindau disease. J Neurosurg. 2009; 110:350–353. PMID: 18834262.
Article
11. Neumann HP, Eggert HR, Weigel K, Friedburg H, Wiestler OD, Schollmeyer P. Hemangioblastomas of the central nervous system. A 10-year study with special reference to von Hippel-Lindau syndrome. J Neurosurg. 1989; 70:24–30. PMID: 2909683.
12. Neumann HP, Wiestler OD. Clustering of features of von Hippel-Lindau syndrome : evidence for a complex genetic locus. Lancet. 1991; 337:1052–1054. PMID: 1673491.
Article
13. Rumboldt Z, Gnjidić Z, Talan-Hranilović J, Vrkljan M. Intrasellar hemangioblastoma : characteristic prominent vessels on MR imaging. AJR Am J Roentgenol. 2003; 180:1480–1481. PMID: 12704075.
Article
14. Sawin PD, Follett KA, Wen BC, Laws ER Jr. Symptomatic intrasellar hemangioblastoma in a child treated with subtotal resection and adjuvant radiosurgery. Case report. J Neurosurg. 1996; 84:1046–1050. PMID: 8847570.
Article
Full Text Links
  • JKNS
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr