1887
Volume 2021, Issue 2
  • ISSN: 0253-8253
  • EISSN: 2227-0426

Abstract

Background: The central nervous system is an unusual location of sarcoidosis, which commonly affects the cranial nerves, meninges, hypothalamus, and pituitary gland. Involvement of the pineal region is extremely rare. This systematic review focused on the diagnosis and management of pineal region sarcoidosis, dorsal mesencephalon, and periaqueductal region.

Objectives: This study aimed to discuss diagnostic modalities and best management tools of the aforementioned pathology.

Methods: ScienceDirect, PubMed, and Google Scholar databases were searched for English or French articles about sarcoidosis of the pineal region, dorsal mesencephalon, and periaqueductal region. The clinical case of a patient managed at our department that we believe is directly relevant to this review is also presented. Patients’ demographics, clinical presentations, presence of hydrocephalus, other sarcoidosis locations in the central nervous system, and medical treatment were collected. Surgical management, surgical approach, and outcomes and complications of each procedure were also obtained. This study was conducted in agreement with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement.

Results: Fifteen cases were examined. The study sample consisted of nine (60%) male and six (40%) female, and the mean age was 32 years. Eight (53%) patients had hydrocephalus, and the predominant clinical presentations were signs of increasing intracranial pressure (headaches, vomiting, and papilledema). Six (40%) patients had diplopia, and convergence–retraction nystagmus was noted in three (20%) patients. Argyll Robertson sign was present in one patient and suspected in another patient (13%). Medical treatment consisted mainly of steroids (93% of cases). Open surgery on the pineal region was performed in five patients, and four of them reported to have serious complications (such as ophthalmoplegia, hemianopsia, hemiparesis, bilateral third cranial nerve paresis, and cerebellar syndrome). Endoscopic management was performed in two patients without complications.

Conclusion: To treat hydrocephalus, brain imaging is mandatory in patients with sarcoidosis if intracranial hypertension is suspected. In pineal region sarcoidosis, management of hydrocephalus is the priority, followed by medical treatment of the lesion. Open surgery of any approach presents a high risk of complications; thus, an endoscopic approach is the preferred management, as it treats hydrocephalus and makes biopsy possible with minimal risk.

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2021-08-23
2024-04-19
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References

  1. Nowak DA, Widenka DC. Neurosarcoidosis a review of its intracranial manifestation. J Neurol 2001 248: 363–372.
    [Google Scholar]
  2. Lacomis D. Neurosarcoidosis. Curr Neuropharmacol 2011 9: 429–436.
    [Google Scholar]
  3. Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. J Clin Epidemiol 2009 62: 1006–1012.
    [Google Scholar]
  4. Schaefer M, Lapra C, Thomalske G, Grau H, Schober R. Sarcoidosis of the pineal gland case report. J Neurosurg 1977 47: 630–632.
    [Google Scholar]
  5. Giroud M, Audry D, Tavernier C, Dumas R. Sarcoïdose disséminée avec une complication neurologique rare la sténose de l‘aqueduc de Sylvius. Rev Med Interne 1983 4: 357–359.
    [Google Scholar]
  6. Poole CJM. Argyll Robertson pupils due to neurosarcoidosis evidence for site of lesion. Br Med J 1984 289: 259.
    [Google Scholar]
  7. Wall MJ, Peyster RG, Finkelstein SD, Pistone WR, Hoover ED. A unique case of neurosarcoidosis with pineal and suprasellar involvement CT and pathological demonstration. J Comput Assist Tomogr 1985 9: 381–383. doi: 10.1097/00004728-198503000-00032.
    [Google Scholar]
  8. Sherman JL, Stern BJ. Sarcoidosis of the CNS comparison of unenhanced and enhanced MR Images. AJNR Am J Neuroradiol 1990 11: 915–923.
    [Google Scholar]
  9. Martin N, Debroucker T, Mompoint D, Akoun J, Cambier J, Nahum H. Sarcoidosis of the pineal region CT and MR studies. J Comput Assist Tomogr 1989 13: 110–112.
    [Google Scholar]
  10. Sattelmeyer V M, Vernet O, Janzer R, de Tribolet N. Neurosarcoidosis presenting as an isolated mass of the quadrigeminal plate. J Clin Neurosci 1999 6: 259–261.
    [Google Scholar]
  11. Klainguti G, Spahn B, Borruat FX. Selective and sequential therapy of oculomotor and palpebral sequelae resulting from biopsy of dorsal midbrain sarcoidosis. Klin Monabl Augenheilkd 2004 221: 404–407. DOI 10.1055/s-2004-812862.
    [Google Scholar]
  12. Oishi A, Miyamoto K, Yoshimura N. Dorsal midbrain syndrome induced by midbrain neurosarcoidosis. Jpn J Ophthalmol 2008 52: 236–238. https://doi.org/10.1007/s10384-007-0529-z.
    [Google Scholar]
  13. Westhout FD, Linskey ME. Obstructive hydrocephalus and progressive psychosis rare presentations of neurosarcoidosis. Surg Neurol 2008 69: 288–292. doi: 10.1016/j.surneu.2007.01.068.
    [Google Scholar]
  14. Yang I, Delpolyi A, Sughrue ME, Rubenstein J, Bollen AW, Parsa AT. Sarcoidosis of the pineal gland an unusual presentation of neurosarcoidosis. J Neurooncol 2009 91: 113–116. doi: 10.1007/s11060-008-9687-1.
    [Google Scholar]
  15. Chandna A, Todd C, Murphy D, Boet R, Duncan R. Sarcoidosis presenting with acute hydrocephalus in a New Zealand European female. N Z Med J 2015 128: 110–113.
    [Google Scholar]
  16. Nakayasu H, Shirai T, Tanaka Y, Sato T, Muro H. Neurosarcoidosis presenting with obstructive hydrocephalus successfully treated with endoscopic third ventriculostomy. Intern Med 2019 58: 105–108. doi: 10.2169/internalmedicine.1259-18.
    [Google Scholar]
  17. O'Connor A, Gilmore D, Shaamile F, McQuaid S. SUN-427 Hypopituitarism as a rare manifestation in a patient with neurosarcoidosis. J Endocr Soc 2019 3: SUN-427. https://doi.org/10.1210/js.2019-SUN-427 .
    [Google Scholar]
  18. Saban RJ, Berns MM, Al-Hakim MM, Patino GA. Hydrocephalus as the presenting symptom of sarcoidosis a case report and review of literature. Clin Case Rep 2020 8: 363–368. https://doi.org/10.1002/ccr3.2665 .
    [Google Scholar]
  19. Byard RW, Manton N, Tsokos M. Sarcoidosis and mechanisms of unexpected death. J Forensic Sci 2008 53: 460–464. doi: 10.1111/j.1556-4029.2008.00662.x.
    [Google Scholar]
  20. Zoja R, Andreola S, Gentile G, Rancati A. Sudden death from systemic sarcoidosis a case of legal medicine. Sarcoidosis Vasc Diffuse Lung Dis 2012 29: 62–68.
    [Google Scholar]
  21. Maisel JA, Lynam T. Unexpected sudden death in a young pregnant woman unusual presentation of neurosarcoidosis. Ann Emerg Med 1996 28: 94.
    [Google Scholar]
  22. Rooijen JMV, Mijnhout GS, Aalders TT, RBJ de. Bondt. Hydrocephalus a rare manifestation of sarcoidosis. Clin Pract 2011 1e66: 136–138. doi: 10.4081/cp.2011.e66.
    [Google Scholar]
  23. Schlitt M, Duvall ER, Bonnin J, Morawetz RB. Neurosarcoidosis causing ventricular loculation hydrocephalus, and death. Surg Neurol 1986 26: 67–71.
    [Google Scholar]
  24. Zajicek JP, Scolding NJ, Foster O, Rovaris M, Evanson J, Moseley IF, et al. Central nervous system sarcoidosis diagnosis and management. QJM 1999 92: 103–117.
    [Google Scholar]
  25. Cipri S, Gangemi A, Cafarelli F, Messina G, Iacopino P, Al Sayyad S, et al. Neuroendoscopic management of hydrocephalus secondary to midline and pineal lesions. J Neurosurg Sci 2005 49: 97–106.
    [Google Scholar]
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  • Article Type: Review Article
Keyword(s): neurosarcoidosispineal region and sarcoidosis
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