Rathke's Cleft Cyst Abscess with a Very Unusual Course

Amy Coulden, Joshua Pepper, Agata Juszczak, Ruchika Batra, Swarupsinh Chavda, Latha Senthil, John Ayuk, Ute Pohl, Santhosh Nagaraju, Niki Karavitaki, Georgios Tsermoulas

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Abstract

Infected Rathke’s cleft cysts (RCC) are extremely rare with only a few published cases. We report the case of a 31-year-old man who presented with headaches, visual disturbance, and hypopituitarism secondary to an infected RCC with extension of abscesses along the optic tract. Magnetic resonance imaging showed ring enhancing cystic lesions within an expanded sella with suprasellar and intraparenchymal extension. The radiological appearance suggested a high-grade optic glioma, but an endoscopic transsphenoidal biopsy revealed frank pus in the pituitary fossa, which subsequently grew Staphylococcus aureus. Pathological examination of the cyst wall showed an inflamed RCC. Following a prolonged course of intravenous antibiotics, the infection resolved and vision improved. RCC abscesses are rare and the intracranial extension of the infection in our case makes it unique.
Original languageEnglish
Pages (from-to)527-531
Number of pages5
JournalAsian Journal of Neurosurgery
Volume17
Issue number3
DOIs
Publication statusPublished - 1 Sept 2022

Keywords

  • Rathke’s cleft cyst
  • pituitary abscess
  • transphenoidal surgery

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