CC BY-NC-ND 4.0 · Indian Journal of Neurosurgery 2022; 11(01): 073-075
DOI: 10.1055/s-0041-1726600
Short Communication

Rathke’s Cleft Cyst Abscess—An Unusual Guest in The Sella

1   Department of Endocrinology, Gandhi Medical College/Gandhi Hospital, Musheerabad, Secunderabad, Hyderabad, India
,
P Rao Srinivas
1   Department of Endocrinology, Gandhi Medical College/Gandhi Hospital, Musheerabad, Secunderabad, Hyderabad, India
,
1   Department of Endocrinology, Gandhi Medical College/Gandhi Hospital, Musheerabad, Secunderabad, Hyderabad, India
,
Gollapudi Prakash Rao
2   Department of Neurosurgery, Gandhi Medical College/Gandhi Hospital, Musheerabad, Secunderabad, Hyderabad, India
› Author Affiliations

Abstract

Abscess formation within a Rathke's cleft cyst (RCC) is extremely rare, particularly at a young age. We report the case of a young girl with abscess formation in RCC. A 21-year-old female presented with headache, vomiting, visual deterioration and features suggestive of hypopituitarism. She had bitemporal hemianopia with impairment of visual acuity. MRI revealed a cystic lesion in the sella with suprasellar extension and peripheral rim enhancement. On the basis of history and imaging, this was indistinguishable from more commonly encountered pituitary pathology. She underwent transsphenoidal decompression, which revealed yellowish purulent material that when cultured grew Staphylococcus epidermidis. Histological examination revealed numerous neutrophils and cyst wall lining with features characteristic of RCC. Postoperatively, she received antibiotics and replacement therapy for hypopituitarism. Three months later, she experienced deterioration in visual fields. Considering persistent disease, she underwent redo surgery which revealed similar findings. Postsurgery, pituitary MRI revealed an empty sella syndrome. Thereafter, follow-up for 1 year was stable with permanent diabetes insipidus and multiple pituitary hormone deficiency on supplementation. Although uncommon, we recommend considering RCC abscess as a differential diagnosis of a pituitary mass lesion, as predicting its presence can be difficult preoperatively. Persistent or recurrent disease is common in these cases, so timely diagnosis and adequate surgical drainage leads to lower morbidity and mortality.



Publication History

Article published online:
24 November 2021

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  • References

  • 1 Vates GE, Berger MS, Wilson CB. Diagnosis and management of pituitary abscess: a review of twenty-four cases. J Neurosurg 2001; 95 (02) 233-241
  • 2 Dalan R, Leow MK. Pituitary abscess: our experience with a case and a review of the literature. Pituitary 2008; 11 (03) 299-306
  • 3 Su YH, Chen Y, Tseng SH. Pituitary abscess. J Clin Neurosci 2006; 13 (10) 1038-1041
  • 4 Komatsu F, Tsugu H, Komatsu M. et al. Clinicopathological characteristics in patients presenting with acute onset of symptoms caused by Rathke’s cleft cysts. Acta Neurochir (Wien) 2010; 152 (10) 1673-1678
  • 5 Uchiyama T, Sakai K, Asanuma M, Aoyama T, Hongo K. Pituitary abscess manifesting as meningitis and photophobia associated with Rathke’s cleft cyst in a child. Case report. Neurol Med Chir (Tokyo) 2011; 51 (06) 455-459
  • 6 Tate MC, Jahangiri A, Blevins L, Kunwar S, Aghi MK. Infected Rathke cleft cysts: distinguishing factors and factors predicting recurrence. Neurosurgery 2010; 67 (03) 762-769
  • 7 Wolansky LJ, Gallagher JD, Heary RF. et al. MRI of pituitary abscess: two cases and review of the literature. Neuroradiology 1997; 39 (07) 499-503
  • 8 Celikoglu E, Boran BO, Bozbuga M. Abscess formation in Rathke’s cleft cyst. Neurol India 2006; 54 (02) 213-214
  • 9 Kim JE, Kim JH, Kim OL. et al. Surgical treatment of symptomatic Rathke cleft cysts: clinical features and results with special attention to recurrence. J Neurosurg 2004; 100 (01) 33-40